Insights of Herbal Supplements during Transition Period in Dairy Animals: An Updated Review

Document Type : Review Article


1 Department of Livestock Production Management, ICAR-National Dairy Research Institute, Karnal, India

2 ICAR-Indian Veterinary Research Institute, Bareilly, India

3 Department of Animal Nutrition, ICAR-National Dairy Research Institute, Karnal, India

4 Department of Animal Physiology, ICAR-National Dairy Research Institute, Karnal, India


There have been unsatisfactory results from antibiotic supplementation in long run for dairy animals. Antibiotic supplementation has been reported to accelerate the risk of antibiotic residues along with posing a potential threat to both human and animal health through compromised food safety. Therefore, there was a need of some alternative and safe supplementation to the dairy animals which may improve their production, reproduction, health, body condition, energy balance, and oxidative status. Herbal feed supplements are being widely used these days and scientists in the field of animal production are continuously devising the incorporation of some un-conventional herbal feed stuff in the diet of dairy animals. Herbal feed supplementation has been found comparatively much safer than any antibiotic or other inorganic feed supplements in farm animals. Transition management of dairy animals for improved post-partum performances has been a prime focus of most of the animal scientists. Transition period has far reaching effects on the post partum performances in regard to production, reproduction, health, body condition, energy balance, and oxidative status of dairy animals. Herbal supplements during transition period are anticipated to bring desired changes in the production, reproduction, health, body condition, energy balance, and oxidative status of dairy animals. Therefore, this review was framed with an aim of presenting a concise yet an informative discussion over the effects of supplementing herbal feed additives to the dairy animals to overview its effects on different production, reproduction and health parameters.



Dairy industry is now focussing more over the quality milk production which is safe for human consumption without any negative impact over the health and performances of dairy animals (Singh et al. 2020a; Singh et al. 2020d; Kansal et al. 2020). Improved dairy performance with maintenance of proper udder health has been the centre of attraction of many animal scientists since long time (Kumari et al. 2019; Kumari et al. 2020; Singh et al. 2020f). Proper management practices for animal husbandry may help in improving and maintaining the performances of dairy animals (Kumari et al. 2020; Singh et al. 2020a; Singh et al. 2020g). There have been detailed studies on the influence of antibiotics and hormonal treatments in farm animals during their transition period (Ludri et al. 1989; Singh and Ludri, 1994; Jyotsna and Singh, 2010; Singh et al. 2012; Mullen et al. 2014). However, it has also been remarked that prolonged utilization of antibiotics and hormonal treatments in farm animals to obtain improved milk yield are associated with health problems like antibiotic residues and hormonal imbalances which leads to poor well being of farm animals (Grosvenor et al. 1993). Nevertheless, supplementation of herbal preparations emerged as useful and efficient possible substitute for use of antibiotics and hormones in dairy animals during late dry period and initial lactation period for desired production performances, reduced subclinical mastitis cases, with minimum negative energy balance in farm animals. It has been reported that there are more than 300 medicinal spices which have been identified in the world (Krishna et al. 2005; Pandey et al. 2005; Singh et al. 2012). Selection of suitable herbs for supplementing to the dairy animals has the potential of improving health and performances of farm animals as shown in Figure 1. Management of dairy animals for the maintenance of their health during whole transition period has been seen to have far reaching effects on the lactation and health performances of dairy animals (Singh et al. 2020h; Singh et al. 2020i; Singh et al. 2020e). Transition period may be explained as last three weeks of dry period to three weeks post partum (Drackley, 1999; Overton and Waldron, 2004; Drackley and Cardoso, 2014). It is a common trend that high producing animals suffer negative energy balance wherein the nutrition requirement of animal escapes the supply of nutrients to the animals by decreased dry matter intake (Singh et al. 2020a; Singh et al. 2020b). McArt et al. (2013) remarked that the management strategies should be driven in such a way that it can suffice the nutrient availability to the animals to combat negative energy balance conditions. Combating negative energy balance in peri-partum animals have shown improved production, reproduction, and health of dairy animals (Ospina et al. 2010; Chapinal et al. 2011; Chapinal et al. 2012; Singh, 2019; Singh et al. 2020a; Singh et al. 2020b). In recent past, dairy sector has experienced tremendous growth resulting in elevation of pressure for intense selection of dairy animals for higher production. This has led to higher incidences of metabolic disorders, and reduced reproductive performances in dairy herds. Excessive negative energy balance due to mobilization of nutrients during transition period is the main reason for most of the production loss and overall profitability of the dairy farms. Transition period (also termed as periparturient period) is the most crucial period in the life of a dairy cow. The period between 3 weeks before parturition to 3 weeks after parturition is considered as transition phase and is very much important for the production, and health status of the dairy cow. During this phase dairy cows are more susceptible for metabolic disorders, and infectious diseases (Drackley, 1999). As the cow changes from gestational non-lactating state to lactating state major nutritional, physiological, immunological, and metabolic changes occur during this phase (Sordillo and Raphael, 2013; Singh et al. 2020e; Singh et al. 2020i ). The cow has to adjust rapidly to increased energy demands for milk production. Substantial amount of lipid is mobilized due to altered energy metabolism in this phase (Drackley, 1999) which might be accompanied by systemic inflammation (Trevisi et al. 2012). Alteration in redox balance has also been observed in early lactation due to metabolic changes occur during the transition phase (Bionaz et al. 2007; Singh et al. 2020c; Singh, 2021a). Recent studies (Koujalagi et al. 2018; Safari et al. 2018; Acharya et al. 2019; Gutiérrez et al. 2019; Kekana et al. 2020) shown that herbal supplementation during transition period may have beneficial effects for dairy animals and hence it may prove to be an important alternative for antibiotics and hormonal treatments for dairy animals (Ludri et al. 1989; Singh and Ludri, 1994; Jyotsna and Singh, 2010; Singh et al. 2012; Mullen et al. 2014). It is a fact that there are several reviews on herbal feeding in dairy animals during lactation periods, however, there is scantiness of informative and yet a concise review paper on the supplementing herbal feeds or herbal preparations to the dairy animals during transition period to highlight its post-partum effects. Therefore, this review was specifically framed to present the insights of herbal feedings to dairy animals during transition period.


Mechanism of action of different compounds of herbs

Mode of actions of herbs supplemented to dairy animals have yet not been fully understood, however, different approaches have been tried to explain the mechanisms of action of such herbs or their bioactive compounds. Chemical compounds produced by herbs are arbitrarily divided into primary and secondary metabolites. Primary metabolites include sugars and fats, commonly found in all plants where as the secondary metabolites or phytochemicals are found in smaller range of plants, sometimes found only in a particular genus or species. These secondary metabolites are categorized into major group of chemicals such as essential oils, alkaloids, tannins, saponins, flavonoids, glycosides, amines and non-protein amino acids. Phytochemicals exert antimicrobial activity through different mechanisms. Tannic acid present in tannins inhibit the growth of gut microbes such as E. coli, Clostridium perfringens, Bacteroides fragilis by deprivation of iron, hydrogen bonding and by non-specific interactions with vital proteins. Besides this, tannins bind to polysaccharides or enzyme promoting inactivation (Paiva et al. 2010). Alkaloid act by inhibition of topoisomerase and inhibit DNA synthesis (Karou et al. 2006). Saponin exhibits antimicrobial activity by forming complexes with sterols that are present in the membrane of micro-organisms.


Figure 1 Potential benefits of herbal supplementation in transition dairy animals


These formations of complexes result in collapse of cells by damaging the membrane (Hashemi and Davoodi, 2011). Essential oils show antimicrobial activity against bacteria E. coli and Clostridium perfringens (Jamroz et al. 2005) but the exact mechanism is poorly understood. It may be due to lipophilic property of essential oil because the terpenoids and phenylpropanoids penetrate the membrane of pathogen and reach the inner part of cells to damage them (Bakkali et al. 2008) or it may be due to the chemical structure of essential oil such as presence of functional group and aromaticity. Flavonoids are polyphenolic phytochemicals having both bactericidal and bacteriostatic properties. They act by damaging cytoplasmic membrane, inhibiting energy metabolism and inhibiting nucleic acids synthesis in microorganisms (Ahmed et al. 2015). Through beneficial actions of compounds of herbs on rumen and gut health, an improved immunity response is obtained in animals’ body. Unwanted depletion of energy towards combating against the effects of invading micro-organisms is relieved. Cell damage in animals’ body is minimized through free radical scavenging action of constituents of herbs (Hashemi and Davoodi, 2011). It can be suggested that there may be no specific mode of action for herbal supplementation; instead, herbs have multi- dimensional beneficial effects in animals’ body.


Effect of herbal feeding during transition phase on production performance

Transition period is very crucial in the life cycle of a dairy cow. During this phase cow require more energy to support the initiation of lactation; however it is challenging because of series of metabolic and physiological changes taking place in transition animals (Drackley, 1999). Overall reduction in feed intake was observed in animals prior to calving (Bertics et al. 1992; Drackley, 1999), and thereafter gradual increase in feed intake was observed in days following parturition (Osborne et al. 2002; Huzzey et al. 2005). The metabolic, nutritional, and physiological changes lead to negative energy balance in transition cows. Many researchers have tried different feed supplementation and feeding regimen to overcome the adverse effects of negative energy balance in transition cows. Poly-herbal mixtures are better alternatives for feed supplementation among various compounds employed to reduce the oxidative stress and to increase the production performance in transition animals (Koujalagi et al. 2018; Safari et al. 2018; Acharya et al. 2019; Gutiérrez et al. 2019; Kekana et al. 2020). Poly-herbal feed supplements are safe to use in animals to increase milk production. Several physiological and metabolic changes occurring during periparturient period leads to reduction in dry matter intake and subsequent decline in milk production (Gross and Bruckmaier, 2019). Dietary supplementation of herbal plant mixture has positive effect of dry matter intake in periparturient period (Hashemzadeh-Cigari et al. 2015). Some studies reported an enhancement of dry matter intake in animals supplemented with dietary pomegranate extracts. Pomegranate by-products are believed to be beneficial in terms of reducing methane production, degradation of ruminal protein, and enhancing propionic acid level (Safari et al. 2018). Body condition score (BCS) depicts the nutritional status of the animals and more loss of BCS is observed immediately after calving owing to intensive mobilization of body reserves towards milk production (Hartwell et al. 2000). The change in body weight and change in BCS were significantly higher in control group of animals as compared to animals supplemented with pomegranate by-products during transition period (Safari et al. 2018). Changes in BCS was lesser in transition animals fed with herbal mixture suggestive of feeding herbal mixture had beneficial effect on mobilization of body reserves (Hashemzadeh-Cigari et al. 2015). The milk yield enhancing effect of Shatavari has been observed through many studies since a long time (Kumar et al. 2008). Patel and Kanitkar (1969) outlined that when of fresh root part of Shatavari was added to the concentrate feed in amount of ½ kilogram per day at milking time, it helps to enhance the milk yield markedly. Relatable results were documented in crossbred cattle in early lactation where feeding of grinded root of Shatavari at the rate of 100 grams every other day helped in substantial improvement in milk yield (Berhane and Singh, 2002). Berhane (2000), observed that when Shatavari was added to the diet of freshly calved crossbred cows at the rate of 100 grams every other day, it helped to induce estrus in 100% of the cows as well as successful conception in 75% cows in the span of 3 months after calving. Milk yield, 4% fat corrected milk and energy corrected milk were significantly higher in transition animals fed with rumen protected choline and green tea extracts (Acharya et al. 2020b). Higher milk production was observed in animals fed with herbal mixture during transition period (Hashemzadeh-Cigari et al. 2015). Although significant difference in milk efficiency (milk yield/dry matter intake) was not observed in animals fed with pomegranate by-products, fat corrected and energy corrected milk yield were significantly higher in animals fed with pomegranate by-products (Safari et al. 2018). An increase in daily average milk yield (by 12.76% over control group), and fat corrected milk yield (by 17.45% over control group) was observed in Murrah buffaloes by feeding poly-herbal mixture (poly-herbal mixture constituted of six herbs, Saunf (Foeniculum vulgare), 25 g; Ajwain (Trachyspermum ammi), 25 g; Methi (Trigonella foenum-graecum), 25 g; Sundh (Zingiber officinale), 25 g; Sowa (Anethum graveolens), 25 g and Cardamom (Elettaria cardamomum), 25 g with 25 gram black salt (Kala Namak) and administered in a single dose) along with butyrate in transition period (Chandra et al. 2017). The increase in milk yield is attributed to the galactopoietics and milk ejection property of poly-herbal mixture which enhances milk production and milk flow in lactating animals. Similarly, Singh et al. (2012) reported an increase of 0.526 kg/day milk yield in Murrah buffaloes supplemented with Asparagus racemosus root powder during transition period. Patel et al. (2013) also reported an increase in milk yield (by 14.2%) in Surti buffaloes by supplementing poly-herbal galactogogue mixture. Inclusion of Scutellaria baicalensis, a kind of fungus which has been traditionally utilised in Chinese medicines, extract in diet of early lactating animals has shown increase in overall milk yield in response to alteration of digestibility, and dynamics of rumen fermentation thereby increasing milk production (Olagaray et al. 2019). Increase in milk yield was observed in dairy animals by supplementing herbal choline, especially in first lactation (Gutiérrez et al. 2019). Feeding of concentrated pomegranate extract had significant effect on increasing milk yield in early lactation (Shabtay et al. 2012). Milk fat content and total solids were higher in transition animals fed with poly-herbal mixture along with butyrate (Chandra et al. 2017). The higher amount of milk fat is attributed to better availability of butyrate (Thomas and Chamberlain, 1988) and lesser lipid mobilization in body of animals supplemented with poly-herbal mixture. Milk constituents such milk fat, milk solids-not-fat, and protein increased in transition cows supplemented with herbal vitamin E and selenium complex (Koujalagi et al. 2020). Dietary supplementation of rumen protected choline and green tea extracts enhanced milk fat and total solid contents transition Karan Fries cows (Acharya et al. 2020b). Rumen protected choline helps in more lipid mobilization towards mammary gland for synthesis of milk fat. Lactating animals supplemented with Moringa oleifera leaf meal have shown increase in milk fat (Kekana et al. 2020) owing to the stimulatory effect of Moringa oleifera on higher fiber digestibility and enhancement of acetate production in rumen (Khalel et al. 2014). The energy status of the cows during pre-parturient period significantly affects the birth weight of calves. Higher birth weight of calves was observed in animals fed with poly-herbal mixture and butyric acid (Barjibhe et al. 2019). Lower amount of negative energy balance in animals fed with poly-herbal mixture reduces the level of insulin which in-turn has glucose sparing effect and this saved energy is deviated for the growth of fetus (Barjibhe et al. 2019). Curvilinear increase (P≤0.05) in milk yield due to addition of cumin seed in the diet of dairy cows at 0, 100, 200 and 300 g/cow/d with values 47.9, 52.5, 55.1 and 53.6 kg/d respectively was observed by Ghafaria et al. (2017). Fat and 4% fat corrected milk yield were not affected by treatment, but all other milk components yield followed the same trend as that of milk yield (P≤0.05). Bipate and Mishra (2020) supplemented the poly herbal mixture prepared from 25g each of Ajwain (Trachyspermum ammi), Saunf (Foeniculum vulgare), Methi (Trigonella foenum-graecum), Sowa (Anethum graveolens), Sundh (Zingiber officinale) and Cardamom (Elettaria cardamomum) in crossbred cows from the day of calving to 10 days postpartum. They reported average enhancement of 21.53% milk yield in treatment group compared to control (6.91%) from 0 to 60th day of lactation. Similarly, Japheth et al. (2019) was also observed increased average total milk in Murrah buffaloes (2642.87±75.45 kg) supplemented with polyherbal mixture as compared to the control group (2292.27±77.65 kg). Furthermore, proportion of animals suspicious for mastitis were also significantly decreased (P<0.05) in treatment group as that of control group. Supplementation of herbal preparation of galactogogue (Sanjivani biokseera) to Kankrej cows at 60 g/day from 4th day of calving for 1-month substantially increased (P<0.05) the average milk yield of 52 days in treatment group (9.34±0.21 L/day) as compared to the control group (7.75±0.26 L/day), without affecting the milk composition (Panchasara et al. 2019). Supplementation of Shatavari containing saponin and tannin at 50 to 100 g/day/animal significantly enhanced the milk production in buffaloes (Tanwar et al. 2008) and crossbred cows (Mirzaei, 2012). Similarly, significant increase (P<0.05) in milk production was recorded due to supplementation of Shatavari powder at 50 g/head/day for 90 days after parturition in lactating crossbred Sahiwal cows (Muwal et al. 2020).


Effect of herbal feeding during transition phase on antioxidant status

Due to increased lipid mobilization during transition period to combat the negative energy balance, the animals are more susceptible to oxidative stress, and inflammatory and immune dysfunction (Sordillo and Mavangira, 2014). These physiological alterations increase the risk of occurrence of metabolic and inflammatory diseases in transition animals. The antioxidants present in the circulatory systems plays a crucial role in maintaining the balance between damage due to oxidative stress and repairing of oxidative damage (Wang et al. 2019). Some of the antioxidants such as glutathione peroxidase, superoxide dismutase (SOD), catalase, glucose-6-phosphate, and glutathione reductase facilitates in the anti-oxidation activity against free radical damage caused by oxidative stress (Reyazuddin et al. 2014). Superoxide dismutase catalyses the conversion of superoxide moleculesinto hydrogen peroxide, which in-turn metabolized to water by glutathione peroxidase, and catalase. Total antioxidant capacity was increased in animals supplemented with rumen protected choline (Salman et al. 2017) and green tea extracts (Acharya et al. 2019). Increased level of blood antioxidant status was observed in transition animals supplemented with rumen protected choline (Sun et al. 2016). The antioxidant capacity of green tea extracts is attributed to the epigallocatechin-3-gallate present in the green tea extracts (Saleh et al. 2014). Thio-barbituric acid reactive substance level was reduced significantly in transition animals supplemented with rumen protected choline and green tea extracts (Acharya et al. 2019) which is an indicative of lesser oxidative stress in transition animals. Oxidation and fatty acid mobilization was reduced in transition animals supplemented with pomegranate by-products indicated by reduced ß-hydroxy butyrate and free fatty acid levels (Safari et al. 2018). Polyphenolic compounds and conjugated fatty acids are responsible for the antioxidant property of the pomegranate by-products (Tzulker et al. 2007). Transition cows supplemented with Moringa oleifera leaf meal shown significantly higher levels of superoxide dismutase, and catalase activity indicating enhanced antioxidant status (Kekana et al. 2020). Reduction in concentration of malondialdehyde (MDA) is suggestive of indicator to lipid peroxidation (Wang et al. 2019). Safari et al. (2018) reported an increase in antioxidant activity, and decrease in level of MDA (indicator of oxidative stress) in transition animals fed with pomegranate by-products, specifically pomegranate seed pulp. High polyphenol content present in Moringa oleifera leaf meal reduced MDA and increased the activity of glutathione peroxidase (Siddhuraju and Becker, 2003). Oxidative stress and lipid peroxidation was less in transition animals supplemented with herbal vitamin E and selenium complex (Koujalagi et al. 2020). In addition, feeding of herbal vitamin E and selenium complex has been observed to increase the level of antioxidants such as superoxide dismutase and reduced glutathione in transition animals. Supplementation of herbal choline (20 g per 100 kg body weight per day) along with herbal liver tonic (10 g per 100 kg body weight per day) has shown to reduce the oxidative stress in transition animals (Koujalagi et al. 2018). Many studies done in India indicated that cumin oils exhibit high antioxidant activity due to presence of flavonoids especially apigenin and luteolin in cumin seeds (Patil et al. 2017; Leung, 1980). Gagandeep et al. (2003) showed that supplementation of cumin seed in mice diet at 2.5 and 5% of diet resulted in increased catalase, superoxide dismutase and decreased glutathione. Furthermore, glutathione reductase and glutathione peroxidase activities were not affected due to cumin supplementation. Juhaimi and Ghafoor (2013) confirmed that addition of extracts of cumin seed has enhanced DPPH (1,1-Diphenyl-2-Picrylhydrazyl) radical scavenging activities when compared to non supplemented animals and cumin seed extracts had antioxidant activity range from 8.25 to 11.24 mg/mL. In both normal and immune suppressed animals, oral administration of cumin resulted in modulation of T-lymphocyte’s expression in a dose dependent manner. It also stimulated the expression of T-cell’s (CD4 and CD8) and Th-1 cytokine’s in cyclosporine-A induced immune suppressed mice and normal mice. The active component of cumin increased the level of depleted T-lymphocytes, reduced the increased corticosterone levels and adrenal glands size and increased the thymus and spleen weight in stress induced immune suppressed animals (Chauhan et al. 2010; Patil et al. 2017).


Effect of herbal feeding during transition phase on reproduction performance:

Transition period is very challenging for the dairy cows as they undergo several environmental and managemental stresses. In addition, they have to cope with the metabolic, physiological, and endocrine changes happening in them during transition period. The resulted negative energy metabolism may reduce the reproductive efficiency through various biological mechanisms (Shabab et al. 2016). In a multiyear evaluation by feeding herbal choline to dairy animals, Gutiérrez et al. (2019) reported an increase in fertility rate in first lactation animals and reduced cases of abortion. The occurrence of post-partum anestrous was less in animals fed with poly-herbal mixture during transition period (Chandra et al. 2019). Feeding of poly-herbal mixture during transitional period reduced the days to first observed heat (commencement of cyclicity) which might be due to early uterine involution and initiation of estrous in animals fed with herbal mixture (Barjibhe et al. 2019; Acharya et al. 2020a). Improved uterine health due to herbal feeding decreases the service period, and improves the conception rate (Barjibhe et al. 2019; Acharya et al. 2020a) and pregnancy rate (Acharya et al. 2020a). There is a high chance of occurrence of reproductive disorders during transition period due to compromised immunity and negative energy balance. The incidences of reproductive disorders were low in transitional animals fed with herbal mixture (Barjibhe et al. 2019; Chandraet et al. 2019; Acharya et al. 2020a). The occurrence of metritis and endometritis were lower in animals supplemented with butyric acid and green tea extracts (Chandraet et al. 2019). Similarly, Acharya et al. (2020a) also observed lesser incidences of uterine infections in animals supplemented with rumen protected choline and green tea extracts during transition period. Anti-inflammatory action along with immuno-modulation property of the herbal mixture was related to the lesser incidences of uterine infection in animals fed with herbal mixture. Negative energy balance occur during transitional phase may delay the involution of uterus. The increased concentration of non-esterified fatty acids (NEFA) during transitional period alters the phagocytic activity of leukocytes thereby making the host more susceptible for uterine infections (Zerbe et al. 2000). Lower level of NEFA concentration was observed in transitional animals fed with poly-herbal mixture as compared to control group of animals (Barjibhe et al. 2019). In addition, retained fetal membranes also delay the involution of uterus and predispose the animals for reproductive infections (Gröhn and Rajala-Schultz 2000). Retention of fetal membranes was lesser in animals fed with poly-herbal mixture during transition period (Ulfina et al. 2015; Barjibhe et al. 2019; Chandra et al. 2019; Acharya et al. 2020a) due to early detachment of placental membranes which might be attributed to the improved host immunity, antioxidant, and metabolic status of animals by feeding herbal mixture. Lower incidence of reproductive disorders in animals fed with poly-herbal mixture was thought to hasten the process of uterine involution. Japheth et al. (2021) investigated the effect of supplementation poly-herbal mixture on reproductive performance in post- partum dairy buffaloes. They observed, significant increase (P<0.05) in the involution rate of cervix and uterus in treatment group, along with this, there was efficient cleansing of lochia. Days to first insemination, service period, and the number of services per conception was reduced in poly-herbal mixture supplemented group as compared to the control group. Number of buffaloes with large ovarian follicles within 28 days post- partum were substantially (P<0.05) higher in treatment group as compared to control group. Chaudhiry et al. (2018) observed that supplementation of combination of Tinospora cordifolia and Randia dumetorum were effective in treatment of anoestrus buffalo heifers. Bipate and Mishra (2020) reported that supplementation of poly-herbal mixture to the crossbred cattle decreased the number of insemination per conception in treatment group (2.38) when compared with un-supplemented group (2.88). Apart from this, substantial reduction (P<0.05) in time required for of foetal membranes expulsion and no case of foetal membrane retention was recorded in treatment group as compared to control. Muwal et al. (2020) reported that average first post-partum oestrus and service period was significantly reduced (P<0.05) due to supplementation of shatavari (Asparagus racemosus) powder at 50 g/head/day for 90 days after parturition in lactating crossbred Sahiwal cows (52.83±1.27 and 90.16±1.44 days) when compared to non supplemented group (77.50±2.50 and 112.50±2.50 days). Shatavari enhances antioxidant activity in the by surging the body levels of ascorbic acid, enzymes like superoxide dismutase and catalase (Bhatnagar et al. 2005).


Effect of herbal feeding during transition phase on udder health

Milk somatic cell count (SCC) is used to assess the quality of milk. Somatic cells are closely related to udder health and quality of milk. In general, somatic cells are secreted to eliminate udder infections and tissue damage during lactation (Hillerton, 1999). Reduction in immunity and other inflammatory conditions may lead to increase in milk SCC during initial stages of lactation (Acharya et al. 2019). The immuno-modulating and anti-inflammatory effect of the herbal feed supplements is thought to boost up the udder immunity thereby decreasing milk SCC (Acharya et al. 2019). Several researches have been conducted to estimate the effect of herbal feeding on udder health but least work has been done to assess its effect during transition period. Feeding of plant additives containing choline can reduce the incidences of both clinical and subclinical mastitis (Gutiérrez et al. 2019). Acharya et al. (2019) reported decline in SCC by supplementing rumen protected choline and green tea extracts in transition period suggestive of positive effect of green tea extracts on immunity, and in addition rumen protected choline provides more methyl groups which will help in building polyamides, improving immunity, and repairing of tissue damage by reducing inflammatory reactions (Bindel et al. 2000). Feeding of poly-herbal mixture along with butyric acid improves the udder health status in transition cows. Significant decline in SCC is observed in animals supplemented with poly-herbal mixture and butyric acid as compared to non supplemented group (Chandra et al. 2017). Feeding of Scutellaria baicalensis extract during early lactation reduced milk somatic cells and also incidences of mastitis in dairy cows (Olagaray et al. 2019). Decline in incidence of mastitis was observed in dairy animals supplemented with herbal mixture (Hashemzadeh-Cigari et al. 2014), and reduction in milk somatic cells in lactating cows fed with Moringa olifera leaf meal (Kekana et al. 2019). Koujalagi et al. (2020) also reported decline in SCC in transition cows supplemented with herbal vitamin E and selenium complex. Shatavari can be helpful in preventing incidences of udder infection in dairy animals (Kumar et al. 2011). The alcoholic solution of shatavari root showed germicidal effect on prime mastitis causing microbes like coliform, pseudomonas, klebsiella and streptococci (Bhatnagar et al. 1961, Ahmad et al. 1998). Plasma level of haptoglobin is generally used as an indicator of systemic inflammation. Haptoglobin concentration in milk will be helpful in detecting clinical and subclinical mastitis (Thomas et al. 2015). Although higher concentration of haptoglobin was observed during first week after calving, supplementation of Scutellaria baicalensis extract had no significant effect on concentration of haptoglobin in milk (Olagaray et al. 2019). Supplementation of herbal vitamin E and selenium complex could reduce the pH and electrical conductivity of milk by reducing seepage of sodium, chlorine, and immunoglobulins from blood to milk (Koujalagi et al. 2020). Feeding of herbal vitamin E has positive effect on the udder health by enhancing antioxidant activity and improving the shelf-life of milk by inhibiting auto-oxidation of milk.



Supplementation of herbal preparation to dairy animals has opened a safer window for dairy herdsman to obtain improved milk quality and quantity from dairy animals. Herbal supplementation is safer in the context that it does not have food safety issues for human health such as antibiotic residues and hormonal imbalances as in the cases of antibiotic or hormonal treatment to dairy animals achieving more milk from them. Transition period supplementation of herbal preparations to farm animals may have far reaching beneficial effects over their production, reproduction, and health performances of dairy animals through channelizing nutrients available to the animal’s body thereby maintaining proper body condition and reduced negative energy balance during transition and initial lactation period. This review is anticipated to provide a basic and yet a concise and informative overview about herbal supplementation during transition period.



Authors show their deep regards to the Directors of ICAR- National Dairy Research Institute, Karnal, India and ICAR- Indian Veterinary Research Institute, Bareilly, India for providing financial assistance in the form of institute fellowships. Authors wish to acknowledge National Library in Dairying, NDRI, Karnal where most of the research findings work was performed.

Acharya P., Lathwal S.S., Baithalu R., Patnaik N., Thul M.R. and Moharana B. (2020a). Supplementing rumen protected choline with green tea extract improves reproductive performances in transition Karan Fries Cows. Indian J. Anim. Res. 54(4), 452-455.
Acharya P., Lathwal S.S., Patnaik N.M. and Moharana B. (2019). Green tea extract along with rumen-protected choline improves immune status by modulating oxidative stress in transition Karan fries cows. Int. J. Livest. Res. 9(9), 46-54.
Acharya P., Lathwal S.S., Singh P., Patnaik N.M. and Moharana B. (2020b). Effect of supplementation with rumen-protected choline and green tea extract on production performance of transition Karan Fries cows. Vet. World. 13(3), 489-494.
Ahmad I., Mehmood Z. and Mohammad F. (1998). Screening of some Indian medicinal plants for their antimicrobial properties. J. Ethnopharmacol. 62(2), 183-193.
Ahmed A., Kaleem M., Ahmed Z. and Shafiq H. (2015). Therapeutic potential of flavonoids and their mechanism of action against microbial and viral infections-A review. Food Res. Int. 77, 221-235.
Bakkali F., Averbeck S., Averbeck D. and Idaomar M. (2008). Biological effects of essential oils-A review. Food Chem. Toxicol. 46, 446-475.
Barjibhe S., Oberoi P.S., Patel B. and Patel P.K. (2019). Improving reproductive efficiency through the supplementation of mustard oil, poly-herbal mixture and butyric acid during the periparturient period in Sahiwal cows. J. Entomol. Zool. Stud. 7(2), 668-673.
Berhane M. (2000). Studies on feeding some indigenous galactopoietics feed supplement on performance of crossbred cows. MS Thesis. Jabalpur, India.
Berhane M. and Singh V.P. (2002). Effect of feeding indigenous galactopoietics feed supplements on milk production in crossbred cows. Indian J. Anim. Sci. 72(7), 609-611.
Bertics S.J., Grummer R.R., Cadorniga-Valino C. and Stoddard E.E. (1992). Effect of prepartum dry matter intake on liver triglyceride concentration and early lactation. J. Dairy Sci. 75(7), 1914-1922.
Bhatnagar M., Sisodia S.S. and Bhatnagar R. (2005). Antiulcer and antioxidant activity of Asparagus racemosus willd and Withania somnifera dunal in rats. Ann. N. Y. Acad. Sci. 1056, 261-278.
Bhatnagar S.S., Santapau H., Desa J.D., Maniar A.C., Ghadially N.C., Solomon M.J., Yellore S. and Rao T.N. (1961). Biological activity of Indian medicinal plants. I. Antibacterial, antitubercular and antifungal action. Indian J. Med. Res. 49, 799-813.
Bindel D.J., Drouillard J.S., Titgemeyer E.C., Wessels R.H. and Löest C.A. (2000). Effects of ruminally protected choline and dietary fat on performance and blood metabolites of finishing heifers. J. Anim. Sci. 78(10), 2497-2503.
Bionaz M., Trevisi E., Calamari L., Librandi F., Ferrari A. and Bertoni G. (2007). Plasma paraoxonase, health, inflammatory conditions, and liver function in transition dairy cows. J. Dairy Sci. 90(4), 1740-1750.
Bipate M. and Misra A.K. (2020). Effect of polyherbal supplementation on milk production and postpartum reproduction in crossbred cattle. Indian J. Dairy Sci. 73(2), 136-139. 
Chandra S., Oberoi P.S., Bhakat M., Yogi R.K., Yadav A., Singh P.K. and Kumar A. (2017). Effect of dietary supplementation of poly-herbal mixture and butyric acid on milk production, milk quality and somatic cell counts of postpartum Murrah buffaloes. Indian J. Anim. Res. 51(5), 892-895.
Chandra S., Oberoi P.S., Gupta A., Singh P.K., Bharti P., Diwakar D., Panchbhai G.J. and Thakur A. (2019). Effect of poly-herbal mixture and butyric acid supplementation on incidances of metritis, endometritis and anestrus in postpartum Murrah buffaloes. J. Entomol. Zool. Stud. 7(1), 1361-1363.
Chapinal N., Carson M., Duffield T.F., Capel M., Godden S., Overton M., Santos J.E. and LeBlanc S.J. (2011). The association of serum metabolites with clinical disease during the transition period. J. Dairy Sci. 94(10), 4897-4903.
Chapinal N., Carson M.E., LeBlanc S.J., Leslie K.E., Godden S., Capel M., Santos J.E., Overton M.W. and Duffield T.F. (2012). The association of serum metabolites in the transition period with milk production and early-lactation reproductive performance. J. Dairy Sci. 95(3), 1301-1309.
Chaudhiry V., Kumar A., Kumar J., Srivastava S., Verma R. and Vijayalakshmy K. (2018). Comparative studies on different herbal medicines for induction of estrus in anoestrus buffalo heifers. Turkish J. Vet. Res2(2), 12-19.
Chauhan P., Satti N.K., Suri K.A., Amina M. and Bani S. (2010). Stimulatory effects of Cuminum cyminum and flavonoid glycoside on cyclosporine-A and restraint stress induced immune- suppression in swiss albino mice. Chem. Biol. Interact. 185, 66-72.
Drackley J.K. (1999). Biology of dairy cows during the transition period: The final frontier? J. Dairy Sci. 82(11), 2259-2273.
Drackley J.K. and Cardoso F.C. (2014). Prepartum and postpartum nutritional management to optimize fertility in high-yielding dairy cows in confined TMR systems. Animal. 8(1), 5-14.
Gagandeep S., Dhanalakshmi S., Mendiz E., Rao A.R. and Kale R.K. (2003). Chemopreventive effects of Cuminum cyminum in chemically induced forestomach and uterine cervix tumours in murine model systems. Nutr. Cancer. 47, 171-180.
Ghafaria M., Foroozandeh Shahrakia A.D., Nasrollahib S.M., Aminib H.R. and Beaucheminc K.A. (2017). Cumin seed improves nutrient intake and milk production by dairy cows. Anim. Feed Sci. Technol. 210, 276-280.
Gröhn Y.T. and Rajala-Schultz P.J. (2000). Epidemiology of reproductive performance in dairy cows. Anim. Reprod. Sci. 60, 605-614.
Gross J.J. and Bruckmaier R.M. (2019). Metabolic challenges in lactating dairy cows and their assessment via established and novel indicators in milk. Animal. 13(1), 75-81.
Grosvenor C.E., Picciano M.F. and Baumrucker C.R. (1993). Hormones and growth factors in milk. Endocr. Rev. 14, 710-728.
Gutiérrez A., Gutiérrez A., Sánchez C. and Mendoza G.D. (2019). Effect of including herbal choline in the diet of a dairy herd; a multiyear evaluation. Emirates J. Food Agric. 31(6), 477-481.
Hartwell J.R., Cecava M.J. and Donkin S.S. (2000). Impact of dietary rumen undegradable protein and rumen-protected choline on intake, peripartum liver triacylglyceride, plasma metabolites and milk production in transition dairy cows. J. Dairy Sci. 83(12), 2907-2917.
Hashemi S.R. and Davoodi H. (2011). Herbal plants and their derivatives as growth and health promoters in animal nutrition. Vet. Res. Commun. 35(3), 169-180.
Hashemzadeh-Cigari F., Ghorbani G.R., Khorvash M., Riasi A., Taghizadeh A. and Zebeli Q. (2015). Supplementation of herbal plants differently modulated metabolic profile, insulin sensitivity, and oxidative stress in transition dairy cows fed various extruded oil seeds. Prev. Vet. Med. 118(1), 45-55.
Hashemzadeh-Cigari F., Khorvash M., Ghorbani G.R., Kadivar M., Riasi A. and Zebeli Q. (2014). Effects of supplementation with a phytobiotics-rich herbal mixture on performance, udder health, and metabolic status of Holstein cows with various levels of milk somatic cell counts. J. Dairy Sci. 97(12), 7487-7497.
Hillerton J.E. (1999). Redefining mastitis based on somatic cell count. Bull. Int. Dairy Fed. 345, 4-6.
Huzzey J.M., Von Keyserlingk M.A.G. and Weary D.M. (2005). Changes in feeding, drinking, and standing behavior of dairy cows during the transition period. J. Dairy Sci. 88(7), 2454-2461.
Jamroz D., Wiliczkiewicz A., Wertelecki T., Orda J. and Sukorupinska J. (2005). Use of active substances of plant origin in chicken diets based on maize and locally grown cereals. British Poult. Sci. 46, 485-493.
Japheth K.P., Kumaresan A., Ganaie B.A., Oberoi P.S., Lathwal S.S. and Singh P. (2019). Effect of polyherbal mixture supplementation on incidence of mastitis and milk production in postpartum Murrah buffaloes. Indian J. Dairy Sci. 72(1), 85-88.
Japheth K.P., Kumaresan A., Patbandha T.K., Baithalu R.K., Selvan A.S., Nag P. and Oberoi P.S. (2021). Supplementation of a combination of herbs improves immunity, uterine cleansing and facilitate early resumption of ovarian cyclicity: A study on post-partum dairy buffaloes. J. Ethnopharmacol272, 113931-113939.
Juhaimi A.L. and Ghafoor K. (2013). Extraction optimization and in vitro antioxidant properties of phenolic compounds from cumin (Cuminum cyminum) seed. Int. Food Res. J. 20, 1669-1675.
Jyotsna P. and Singh M. (2010). Effect of bromocryptine on hormones and milk secretion in Murrah buffaloes (Bubalus bubalis). Animal. 4, 772-776.
Kansal G., Yadav D.K., Singh A.K. and Rajput M.S. (2020). Advances in the management of bovine mastitis. Int. J. Adv. Agric. Sci. Technol. 7(2), 10-22.
Karou D., Savadogo A., Canini A., Yameogo S., Montesano C., Simpore J., Colizzi V. and Traore A.S. (2006). Antibacterial activity of alkaloids from Sida acuta. African J. Biotechnol. 5, 195-200.
Kekana T.W., Marume U., Muya C.M. and Nherera-Chokuda F.V. (2019). Lactation performance and blood metabolites in lactating dairy cows micro-supplemented with Moringaoleifera leaf meal. South African J. Anim. Sci. 49(4), 709-716.
Kekana T.W., Marume U., Muya M.C. and Nherera-Chokuda F.V. (2020). Periparturient antioxidant enzymes, haematological profile and milk production of dairy cows supplemented with Moringa oleifera leaf meal. Anim. Feed Sci. Technol. 268, 114606-114612.
Khalel M.S., Shwerab A.M., Hassan A.A., Yacout M.H., El-Badawi A.Y. and Zaki M.S. (2014). Nutritional evaluation of Moringaoleifera fodder in comparison with Trifolium alexandrinum (berseem) and impact of feeding on lactation performance of cows. Life Sci. J. 11(10), 1040-1054.
Koujalagi S., Chhabra S., Randhawa S.N.S., Singh R. and Gupta D.K. (2020). Effect of herbal vitamin E and organic selenium complex supplementation on oxidative stress, milk quality and somatic cell count in transition dairy cows. J. Entomol. Zool. Stud. 8(4), 660-665.
Koujalagi S., Chhabra S., Randhawa S.N.S., Singh R., Randhawa C.S. and Kashyap N. (2018). Effect of herbal bio choline supplementation on oxidative stress and biochemical parameters in transition dairy cows. J. Pharm. Innov. 7(4), 842-847.
Krishna L., Swarup D. and Patra R.C. (2005). An overview of prospects of ethno-veterinary medicine in India. Indian J. Anim. Sci. 75, 1481-1491.
Kumar S., Mehla R. and Dang A. (2008). Use of Shatavari (Asparagus racemosus) as a galactopoietic and therapeuticherb- A review. Agric. Rev. 29(2), 132-138.
Kumar S., Mehla R.K. and Menna R.K. (2011). Pre-and-postpartum managemental intervention through herbal feed supplement (Asparagus racemosus) and its effect on production and reproduction performance during supplementation and post-supplementation period in crossbred cows. Indian J. Anim. Sci. 81, 669-675.
Kumari T., Bhakat C. and Singh A.K. (2020). Adoption of management practices by the farmers to control sub clinical mastitis in dairy animals. J. Entomol. Zool. Stud. 8(2), 924-927.
Kumari T., Bhakat C., Singh A.K., Sahu J., Mandal D.K. and Choudhary R.K. (2019). Low cost management practices to detect and control sub-clinical mastitis in dairy cattle. Int. J. Curr. Microbiol. Appl. Sci. 8(5), 1958-1964.
Leung A.Y. (1980). Encyclopedia of common natural ingredients used in food, drugs, and cosmetics. Wiley, New York, USA.
Ludri R.S., Upadhyay R.C., Singh M., Guneratne J.R. and Basson R.P. (1989). Milk production in buffaloes receiving recombinant produced bovine somatotropin (BST). J. Dairy Sci. 72, 2283-2287.
McArt J.A.A., Nydam D.V. and Oetzel G.R. (2013). Dry period and parturient predictors of early lactation hyperketonemia in dairy cattle. J. Dairy Sci. 96(1), 198-209.
Mirzaei F. (2012). Effect of herbal feed additives on performance parameters of ruminants and especially on dairy goat: A review. Int. J. Agro Vet. Med. Sci. 6, 307-331.
Mullen K.A.E., Anderson K.L. and Washburn S.P. (2014). Effect of 2 herbal intra-mammary products on milk quantity and quality compared with conventional and no dry cow therapy. J. Dairy Sci. 97, 3509-3522.
Muwal H., Rai D.C., Bhateshwar V., Lal D. and Nehra H.L. (2020). Effect of herbal feed supplementation shatavari (Asparagus racemosus) on milk yield and post-partum estrus in lactating sahiwal crossbred cows. Int. J. Curr. Microbiol. App. Sci. 9(2), 2921-2928.
Olagaray K.E., Brouk M.J., Mamedova L.K., Sivinski S.E., Liu H., Robert F., Dupuis E., Zachut M. and Bradford B.J. (2019). Dietary supplementation of Scutellaria baicalensis extract during early lactation decreases milk somatic cells and increases whole lactation milk yield in dairy cattle. PLoS One. 14(1), e0210744.
Osborne V.R., Leslie K.E. and McBride B.W. (2002). Effect of supplementing glucose in drinking water on the energy and nitrogen status of the transition dairy cow. Canadian J. Anim. Sci. 82(3), 427-433.
Ospina P.A., Nydam D.V., Stokol T. and Overton T.R. (2010). Associations of elevated nonesterified fatty acids and β-hydroxybutyrate concentrations with early lactation reproductive performance and milk production in transition dairy cattle in the northeastern United States. J. Dairy Sci. 93(4), 1596-1603.
Overton T.R. and Waldron M.R. (2004). Nutritional management of transition dairy cows: Strategies to optimize metabolic health. J. Dairy Sci. 87, 105-119.
Paiva P.M.G., Gomes F.S., Napoleão T.H., Sá R.A., Correia M.T.S. and Coelho L.C.B.B. (2010). Antimicobial activity of secondary metabolites and lectins from plants. Pp. 396-406 in Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology. Formatex Research Center. Badajoz, Spain.
Panchasara H.H., Chaudhari A.B., Patel D.A., Gami Y.M. and Patel M.P. (2019). Effect of herbal galactogogue (Sanjivani biokseera) on milk yield and milk constituents in lactating Kankrej cattle at organised farm. Indian J. Vet. Sci. Biotechl. 15(2), 38-40.
Pandey S.K., Sahay A., Pandey R.S. and Tripathi Y.B. (2005). Effect of Asparagus racemosus rhizome (Shatavari) on mammary gland and genital organs of pregnant rat. Phytother. Res. 19, 721-724.
Patel A.B. and Kanitkar U.K. (1969). Asparagus racemosuswilld-form bordi, as a galactogogue, in buffaloes. Indian Vet. J. 46(8), 718-721.
Patel M.D., Tyagi K.K., Sorathiya L.M. and Fulsoundar A.B. (2013). Effect of polyherbalgalactogogue supplementation on milk yield and quality as well as general health of Surti buffaloes of south Gujarat. Vet. World. 6(4), 214-218.
Patil A.K., Baghel R.P.S., Nayak S., Malapure C.D., Govil K., Kumar D. and Yadav P.K. (2017). Cumin (Cuminum cyminum): As a feed additive for livestock. J. Entomol. Zool. Stud. 5(3), 365-369.
Reyazuddin M., Azmi S.A., Islam N. and Rizvi A. (2014). Oxidative stress and level of antioxidant enzymes in drug-naive schizophrenics. Indian J. Psychiatry. 56(4), 344-349.
Safari M., Ghasemi E., Alikhani M. and Ansari-Mahyari S. (2018). Supplementation effects of pomegranate by-products on oxidative status, metabolic profile, and performance in transition dairy cows. J. Dairy Sci. 101(12), 11297-11309.
Saleh F., Raghupathy R., Asfar S., Oteifa M. and Al-Saleh N. (2014). Analysis of the effect of the active compound of green tea (EGCG) on the proliferation of peripheral blood mononuclear cells. BMC Complement. Altern. Med. 14(1), 322-328.
Salman M., Çiftçi G. and Ciftci A. (2017). Influence of rumen-protected choline on blood red-ox potential and biochemical biomarkers of dairy cows during the transition period. Vet. Med. 73(8), 483-487.
Shabab K., Singh M., Mehla R.K., Thakur S. and Meena B.S. (2016). Plasma hormones and milk production performances in early lactation buffaloes supplemented with a mixture of prilled fat, sweetener and toxin binder. Biotechnol. Anim. Husb. 32(1), 15-26.
Shabtay A., Nikbachat M., Zenou A., Yosef E., Arkin O., Sneer O., Shwimmer A., Yaari A., Budman E., Agmon G. and Miron J. (2012). Effects of adding a concentrated pomegranate extract to the ration of lactating cows on performance and udder health parameters. Anim. Feed Sci. Technol. 175(2), 24-32.
Siddhuraju P. and Becker K. (2003). Antioxidant properties of various solvent extracts of total phenolic constituents from three different agroclimatic origins of drumstick tree (Moringa oleifera) leaves. J. Agric. Food. Chem. 51(8), 2144-2155.
Singh A.K. (2019). Influence of alteration of management practice on performances of dairy cows at lower Gangetic region. MS Thesis. Karnal, India.
Singh A.K. (2021a). Advancements in management practices from far-off dry period to initial lactation period for improved production, reproduction, and health performances in dairy animals: A review. Int. J. Livest. Res. 11(3), 25-41.
Singh A.K., Bhakat C., Kumari T., Mandal D.K., Chatterjee A. and Dutta T.K. (2020a). Influence of alteration of dry period feeding management on body weight and body measurements of Jersey crossbred cows at lower Gangetic region. J. Anim. Res. 10(1), 137-141.
Singh A.K., Bhakat C., Kumari T., Mandal D.K., Chatterjee A., Karunakaran M. and Dutta T.K. (2020b). Influence of pre and postpartum alphatocopherol supplementation on milk yield, milk quality and udder health of Jersey crossbred cows at tropical lower Gangetic region. Vet. World. 13, 2006-2011.
Singh A.K., Bhakat C., Mandal D.K. and Chatterjee A. (2020c). Effect of pre and postpartum alpha-tocopherol supplementation on body condition and some udder health parameters of Jersey crossbred cows at tropical lower Gangetic region. J. Anim. Res. 10(5), 697-703.
Singh A.K., Bhakat C., Mandal D.K., Mandal A., Rai S., Chatterjee A. and Ghosh M.K. (2020d). Effect of reducing energy intake during dry period on milk production, udder health and body condition score of Jersey crossbred cows at tropical lower Gangetic region. Trop. Anim. Health Prod. 52, 1759-1767.
Singh A.K., Bhakat C., Mohammad A., Chatterjee A., Karunakaran M. and Ghosh M.K. (2020e). Economic analysis of pre and postpartum alphatocopherol supplementation for milk performance and dry matter intake of dairy cows in tropical region. Int. J. Livest. Res. 10(10), 137-143.
Singh A.K., Bhakat C., Yadav D.K., Kansal G. and Rajput M.S. (2020f). Importance of measuring water intake in dairy animals: A review. Int. J. Adv. Agric. Sci. Technol. 7(2), 23-30.
Singh A.K., Bhakat C., Yadav D.K., Kumari T., Mandal D.K., Rajput M.S. and Bhatt N. (2020g). Effect of pre and postpartum alphatocopherol supplementation on body measurements and its relationship with body condition, milk yield, and udder health of Jersey crossbred cows at tropical lower Gangetic region. J. Entomol. Zool. Stud. 8(1), 1499-1502.
Singh A.K., Kumari T., Rajput M.S., Baishya A., Bhatt N. and Roy S. (2020h). Review on effect of bedding material on production, reproduction and health of dairy animals. Int. J. Livest. Res. 10, 11-20.
Singh A.K., Yadav D.K., Bhatt N., Sriranga K.R. and Roy S. (2020i). Housing management for dairy animals under Indian tropical type of climatic conditions-a review. Vet. Res. Int. 8(2), 94-99.
Singh M. and Ludri R.S. (1994). Plasma growth hormone profile and milk yield responses of Murrah buffaloes treated with slow release formulation of somidobove. Buffalo J. 10, 81-84.
Singh S.P., Mehla R.K. and Singh M. (2012). Plasma hormones, metabolites, milk production, and cholesterol levels in Murrah buffaloes fed with Asparagus racemosus in transition and postpartum period. Trop. Anim. Health Prod. 44(8), 1827-1832.
Sordillo L.M. and Mavangira V. (2014). The nexus between nutrient metabolism, oxidative stress and inflammation in transition cows. Anim. Prod. Sci. 54(9), 1204-1214.
Sordillo L.M. and Raphael W. (2013). Significance of metabolic stress, lipid mobilization, and inflammation on transition cow disorders. Vet. Clin. North Am. Food Anim. 29(2), 267-278.
Sun F., Cao Y., Cai C., Li S., Yu C. and Yao J. (2016). Regulation of nutritional metabolism in transition dairy cows: Energy homeostasis and health in response to post-ruminal choline and methionine. PLoS One. 11(8), e0160659.
Tanwar P.S., Rathore S.S. and Kumar Y. (2008). Effect of shatavari (Asparagus recemosus) on milk production in dairy animals. Indian J. Anim. Res. 42(3), 232-233.
Thomas F.C., Waterston M., Hastie P., Parkin T., Haining H. and Eckersall P.D. (2015). The major acute phase proteins of bovine milk in a commercial dairy herd. BMC Vet. Res. 11(1), 207-2015.
Thomas P.C. and Chamberlain D.G. (1988). Manipulation of milk composition to meet market needs. Pp. 198-220 in Recent developments in ruminant nutrition 2/editors. W. Haresign and D.J.A. Cole, Eds. Butterworth-Heinemann, Elsevier, United Kingdom.
Trevisi E., Amadori M., Cogrossi S., Razzuoli E. and Bertoni G. (2012). Metabolic stress and inflammatory response in high-yielding, periparturient dairy cows. Res. Vet. Sci. 93(2), 695-704.
Tzulker R., Glazer I., Bar-Ilan I., Holland D., Aviram M. and Amir R. (2007). Antioxidant activity, polyphenol content, and related compounds in different fruit juices and homogenates prepared from 29 different pomegranate accessions. J. Agric. Food Chem. 55(23), 9559-9570.
Ulfina G.G., Kimothi S.P., Oberoi P.S., Baithalu R.K., Kumaresan A., Mohanty T.K., Imtiwati P. and Dang A.K. (2015). Modulation of post partum reproductive performance in dairy cows through supplementation of longor short chain fatty acids during transition period. J. Anim. Physiol. Anim. Nutr. 99(6), 1056-1064.
Wang Y.Z., Li Y., Xu Q.B., Zhang X.Y., Zhang G.N., Lin C. and Zhang Y.G. (2019). Effects of Acremonium terricola culture on production performance, antioxidant status, and blood biochemistry in transition dairy cows. Anim. Feed Sci. Technol. 256, 114261-114269.
Zerbe H., Schneider N., Leibold W., Wensing T., Kruip T.A.M. and Schuberth H.J. (2000). Altered functional and immunophenotypical properties of neutrophilic granulocytes in postpartum cows associated with fatty liver. Theriogenology. 54(5), 771-786.