Effects of Dietary Supplementation of Saccharomyces cerevisiae on Milk Production, Oxidative Stress, and Blood Metabolites of Holstein Dairy Cows during Summer Season
محورهای موضوعی : CamelF. Sehati 1 , A. Towhidi 2 , M. Zhandi 3 , M. Ganjkhanlou 4 , A.H. Nasiri 5 , F. Parnian-Khajehdizaj 6
1 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
2 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
3 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
4 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
5 - Department of Animal Science, College of Agriculture and Natural Resources, University of Tehran, Karaj, Iran
6 - Department of Animal Science, Faculty of Agriculture, University of Tabriz, Tabriz, Iran
کلید واژه: cattle, Probiotic, Oxidative stress, Yeast, <i>Saccharomyces cerevisiae</i>, summer season, yealth,
چکیده مقاله :
The effects of dietary live Saccharomyces cerevisiae as a probiotic on milk production, oxidant/antioxidant status, and lipid metabolism of Holstein dairy cows through the transition and early lactation period during the summer season were investigated. Twelve lactating multiparous dairy cows were randomly allocated to two dietary treatments (n=6) including a control and probiotic-fed groups. Blood samples were collected on days -21, 0, 14, 28, 42, 60 days relative to parturition and analyzed for calcium, iron, cholesterol, triglyceride, low-density lipoprotein, high-density lipoprotein, total antioxidant capacity, malondialdehyde, and albumin. Serum concentrations of triglycerides, cholesterol, and low-density lipoprotein were lower in the probiotic-fed cows compared to those offered the control diet. Albumin concentration did not differ between the groups. The contents of total antioxidant capacity and high-density lipoprotein in the yeast-fed group was greater than the control group (P=0.01 and 0.02, respectively). In addition, serum calcium and iron tended to be higher in the yeast-fed group (P=0.08). Malondialdehyde level did not change between groups, but there was a decrease at calving time in the probiotic-fed group. Yeast-fed cows produced more milk and had higher concentrations of milk fat and non-fat solids than control cows (P<0.05). Rectal temperature was lower in the probiotic-fed group on parturition day. In conclusion, dietary supplementation of Saccharomyces cerevisiae in dairy cows may be a beneficial strategy to alleviate the heat stress and improve the antioxidative defense system and milk production during the transition and the early lactating period.
Abuelo A., Hernández J., Benedito J.L. and Castillo C. (2013). Oxidative stress index (OSi) as a new tool to assess redox status in dairy cattle during the transition period. J. Anim. 7, 1374-1378.
Amundson J.L., Mader T.L., Rasby R.J. and Hu Q.S. (2006). Environmental effects on pregnancy rate in beef cattle. J. Anim. Sci. 84(12), 3415-3420.
Bami M.H., Mohri M., Seifi H.A. and Tabatabaee A.A.A. (2008). Effects of parenteral supply of iron and copper on hematology, weight gain, and health in neonatal dairy calves. Vet. Res. Commun. 32(7), 553-561.
Baumgard L.H. and Rhoads Jr R.P. (2013). Effects of heat stress on postabsorptive metabolism and energetics. Annu. Rev. Anim. Biosci. 1(1), 311-337.
Begley M., Hill C. and Gahan C.G.M. (2006). Bile salt hydrolase activity in probiotics. Appl. Environ. Microbiol. 72(3), 1729-1738.
Benzie I.F.F. and Strain J.J. (1996). The ferric reducing ability of plasma (FRAP)as a measure of “antioxidant power”: the FRAP assay. Anal. Biochem. 239, 70-76.
Berridge M.J. (2012). Calcium signalling remodelling and disease. Biochem. Soc. Trans. 40, 297-309.
Bhimte A., Konyak Y., Balamurugan B. and Singh L.K. (2018). Effect of supplementation of antioxidant (vitamin E ), trace minerals (selenium, copper, zinc) and increased energy allowance on (certain) serum metabolites and competence of transition crossbred cows. Int. J. Curr. Microbiol. Appl. Sci. 7(7), 439-447.
Bourdon E. and Blache D. (2001). The importance of proteins in defense against oxidation. J. Antioxid. Redox Signal. 3(2), 293-311.
Bruno R.G.S., Rutigliano H.M., Cerri R.L., Robinson P.H. and Santos J.E.P. (2009). Effect of feeding Saccharomyces cerevisiae on performance of dairy cows during summer heat stress. Anim. Feed Sci. Technol. 150, 175-186.
Callaway E.S. and Martin S.A. (1997). Effects of a Saccharomyces cerevisiae culture on ruminal bacteria that utilize lactate and digest cellulose. J. Dairy Sci. 80, 2035-2044.
Castillo C., Hernandez J., Bravo A., Pereira V. and Benedito J.L. (2005). Oxidative status during late pregnancy and early lactation in dairy cows. Vet. J. 169(2), 286-292.
Dehghan-Banadaky M., Ebrahimi M., Motameny R. and Heidari S.R. (2013). Effects of live yeast supplementation on mid-lactation dairy cows performances, milk composition, rumen digestion and plasma metabolites during hot season. J. Appl. Anim. Res. 41(2), 137-142.
De Rensis F., Garcia-Ispierto I. and López-Gatius F. (2015). Seasonal heat stress: Clinical implications and hormone treatments for the fertility of dairy cows. Theriogenology. 84(5), 659-666.
Eisenberg S. (1984). High density lipoprotein metabolism. J. Lipid Res. 25(10), 1017-1058.
Erasmus L.J., Robinson P.H., Ahmadi A., Hinders R. and Garrett J.E. (2005). Influence of prepartum and postpartum supplementation of a yeast culture and monensin, or both, on ruminal fermentation and performance of multiparous dairy cows. Anim. Feed Sci. Technol. 122, 219-239.
Giraffa G., Chanishvili N. and Widyastuti Y. (2010). Importance of lactobacilli in food and feed biotechnology. Res. Microbiol. 161(6), 480-487.
Görlach A., Bertram K., Hudecova S. and Krizanova O. (2015). Calcium and ROS: A mutual interplay. Redox Biol. 6, 260-271.
Holmström K.M. and Finkel T. (2014). Cellular mechanisms and physiological consequences of redox-dependent signalling. Nat. Rev. Mol. Cell Biol. 15(6), 411-418.
Huber J.T., Higginbotham G., Gomez-Alarcon R.A., Taylor R.B., Chen K.H., Chan S.C. and Wu Z. (1994). Heat stress interactions with protein, supplemental fat, and fungal cultures. J. Dairy Sci. 77, 2080-2090.
Kankofer M. (2002). Placental release/retention in cows and its relation to peroxidative damage of macromolecules. J. Reprod. Domest. Anim. 37(1), 27-30.
Kapila S. and Sinha P. (2006). Antioxidative and hypocholesterolemic effect of Lactobacillus casei ssp casei (biodefensive properties of lactobacilli). Indian J. Med. Sci. 60(9), 361-368.
Kapusta A., Kuczyńska B. and Puppel K. (2018). Relationship between the degree of antioxidant protection and the level of malondialdehyde in high-performance Polish Holstein-Friesian cows in peak of lactation. PLoS One. 13(3), e0193512.
Karimi A., Mohammadi-Kamalabadi M., Rafieian-Kopaei M. and Amjad L. (2016). Determination of antioxidant activity, phenolic contents and antiviral potential of methanol extract of Euphorbia spinidens bornm (Euphorbiaceae). Trop. J. Pharm. Res. 15(4), 759-764.
Lambert G.P. (2009). Stress-induced gastrointestinal barrier dysfunction and its inflammatory effects. J. Anim. Sci. 87, 101-108.
Li S., Yoon I., Scott M., Khafipour E. and Plaizier J.C. (2016). Impact of Saccharomyces cerevisiae fermentation product and subacute ruminal acidosis on production, inflammation, and fermentation in the rumen and hindgut of dairy cows. Anim. Feed Sci. Technol. 211, 50-60.
Lim D.H., Han M.H., Ki K.S., Kim T.I., Park S.M., Kim D.H. and Kim Y. (2021). Changes in milk production and blood metabolism of lactating dairy cows fed Saccharomyces cerevisiae culture fluid under heat stress. J. Anim. Sci. Technol. 63(6), 1433-1439.
Morrison S.R. (1983). Ruminant heat stress: Effect on production and means of alleviation. J. Anim. Sci. 57, 1594-1600.
NRC. (2001). Nutrient Requirements of Dairy Cattle. 7th Ed. National Academy Press, Washington, DC., USA.
Paik D.C., Wendel T.D. and Freeman H.P. (2005). Cured meat consumption and hypertension: An analysis from NHANES III (1988-1994). Nutr. Res. 25, 1049-1060.
Salvati G.G.S., Júnior N.N.M., Melo A.C.S., Vilela R.R., Cardoso F.F., Aronovich M., Pereira R.A.N. and Pereira M.N. (2015). Response of lactating cows to live yeast supplementation during summer. J. Dairy Sci. 98(6), 4062-4073.
Samli H.E., Senkoylu N., Koc F., Kanter M. and Agma A. (2007). Effects of Enterococcus faecium and dried whey on broiler performance, gut histomorphology and intestinal microbiota. Arch. Anim. Nutr. 61(1), 42-49.
SAS Institute. (2001). SAS®/STAT Software, Release 8.2. SAS Institute, Inc., Cary, NC. USA.
Sauer H., Wartenberg M. and Hescheler J. (2001). Reactive oxygen species as intracellular messengers during cell growth and differentiation. Cell. Physiol. Bioch. 11(4), 173-186.
Saxton A.M. (1998). A macro for converting mean separation output to letter groupings. Pp. 1243-1246 in Proc. 23rd SAS User Group Int., SAS Institute, Cary, North Carolina.
Spady D.K., Woollett L.A. and Dietschy J.M. (1993). Regulation of plasma LDL-cholesterol levels by dietary cholesterol and fatty acids. Annu. Rev. Nutr. 13(1), 355-381.
Stein D.R., Allen D.T., Perry E.B., Bruner J.C., Gates K.W., Rehberger T.G., Mertz K., Jones D. and Spicer L.J. (2006). Effects of feeding propionibacteria to dairy cows on milk yield, milk components, and reproduction. J. Dairy Sci. 89(1), 111-125.
Taranto M.P., Medici M., Perdigon G., Holgado A.P.R. and Valdez G.F. (1998). Evidence for hypocholesterolemic effect of Lactobacillus reuteri in hypercholesterolemic mice. J. Dairy Sci. 81(9), 2336-2340.
Upadhyay N., Kumar A., Lal D., Kant R. and Goyal A. (2018). Detection of groundnut oil and goat body fat adulteration in ghee using principal component analysis on fatty acid profile. Indian J. Dairy Sci. 71(5), 464-472.
Woodford F.P. and Whitehead T.P. (1998). Is measuring serum antioxidant capacity clinically useful? Ann. Clin. Biochem. 35, 48-56.
Yoo J., Maeng H., Sun Y., Kim Y., Park D., Park T.S., Lee S.T. and Choi J. (2009). Oxidative status in iron‐deficiency anemia. J. Clin. Lab. Anal. 23(5), 319-323.
Yoshioka T., Kawada K., Shimada T. and Mori M. (1979). Lipid peroxidation in maternal and cord blood and protective mechanism against activated-oxygen toxicity in the blood. American J. Obst. Gynecol. 135(3), 372-376.
Yuan K., Mendonca L.G.D., Hulbert L.E., Mamedova L.K., Muckey M.B., Shen Y., Elrod, C.C. and Bradford B.J. (2015). Yeast product supplementation modulated humoral and mucosal immunity and uterine inflammatory signals in transition dairy cows. J. Dairy Sci. 98, 3236-3246.
Zaworski E.M., Shriver-Munsch C.M., Fadden N.A., Sanchez W.K., Yoon I. and Bobe G. (2014). Effects of feeding various dosages of Saccharomyces cerevisiae fermentation product in transition dairy cows. J. Dairy Sci. 97, 3081-3098.
Zhu W., Zhang B.X., Yao K.Y., Yoon I., Chung Y.H., Wang J.K. and Liu J.X. (2016). Effects of supplemental levels of Saccharomyces cerevisiae fermentation product on lactation performance in dairy cows under heat stress. Asian-Australasian J. Anim. Sci. 29, 801-806.
Zimbelman R.B., Rhoads R.P., Rhoads M.L., Duff G.C., Baumgard L.H. and Collier R.J. (2009). A re-evaluation of the impact of temperature humidity index (THI) and black globe humidity index (BGHI) on milk production in high producing dairy cows. Pp. 158-169 in Proc. 24th Southwest Nutr. Conf., Arizona, USA.
