Shwartz G, Rhoads ML, VanBaale MJ, Rhoads RP, Baumgard LH. Effects of a supplemental yeast culture on heat-stressed lactating Holstein cows. J Dairy Sci. 2009;92:935–42. https://doi.org/10.3168/jds.2008-1496.
Wheelock JB, Rhoads RP, VanBaale MJ, Sanders SR, Baumgard LH. Effects of heat stress on energetic metabolism in lactating Holstein cows. J Dairy Sci. 2010;93:644–55. https://doi.org/10.3168/jds.2009-2295.
Rhoads ML, Rhoads RP, VanBaale MJ, Collier RJ, Sanders SR, Weber WJ, et al. Effects of heat stress and plane of nutrition on lactating Holstein cows: I. Production, metabolism, and aspects of circulating somatotropin. J Dairy Sci. 2009;92(5):1986–97. https://doi.org/10.3168/jds.2008-1641.
Capuco AV, Ellis SE, Hale SA, Long E, Erdman RA, Zhao X, et al. Lactation persistency: insights from mammary cell proliferation studies. J Anim Sci. 2003;81(Suppl 3):18–31. https://doi.org/10.2527/2003.81suppl_318x.
Tao S, Orellana RM, Weng X, Marins TN, Dahl GE, Bernard JK. Symposium review: The influences of heat stress on bovine mammary gland function. J Dairy Sci. 2018;101:5642–54. https://doi.org/10.3168/jds.2017-13727.
Capuco AV, Choudhary RK. Symposium review: Determinants of milk production: Understanding population dynamics in the bovine mammary epithelium. J Dairy Sci. 2020;103:2928–40. https://doi.org/10.3168/jds.2019-17241.
Slimen IB, Najar T, Ghram A, Dabbebi H, Ben Mrad M, Abdrabbah M. Reactive oxygen species, heat stress and oxidative-induced mitochondrial damage. A review Int J Hyperthermia. 2014;30:513–23. https://doi.org/10.3109/02656736.2014.971446.
Farmer C, Trottier NL, Dourmad JY. Review: Current knowledge on mammary blood flow, mammary uptake of energetic precursors and their effects on sow milk yield. Can J Anim Sci. 2008;88:195–204. https://doi.org/10.4141/CJAS07074.
Sano H, Ambo K, Tsuda T. Blood glucose kinetics in whole body and mammary gland of lactating goats exposed to heat. J Dairy Sci. 1985;68:2557–64. https://doi.org/10.3168/jds.S0022-0302(85)81137-1.
Lublin A, Wolfenson D. Lactation and pregnancy effects on blood flow to mammary and reproductive systems in heat-stressed rabbits. Comp Biochem Physiol A Physiol. 1996;115:277–85. https://doi.org/10.1016/s0300-9629(96)00060-6.
Zeng J, Cai J, Wang DM, Liu HY, Sun HZ, Liu JX. Heat stress affects dairy cow health status through blood oxygen availability. J Anim Sci Biotechnol. 2023;14:112. https://doi.org/10.1186/s40104-023-00915-3.
Richard MJ, Portal B, Meo J, Coudray C, Hadjian A, Favier A. Malondialdehyde kit evaluated for determining plasma and lipoprotein fractions that react with thiobarbituric acid. Clin Chem. 1992;38(5):704–9. https://doi.org/10.1093/clinchem/38.5.704.
Benzie IF, Strain JJ. The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem. 1996;239(1):70–6. https://doi.org/10.1006/abio.1996.0292.
Mepham TB. Amino acid utilization by lactating mammary gland. J Dairy Sci. 1982;65:287–98. https://doi.org/10.3168/jds.S0022-0302(82)82191-7.
Cant JP, DePeters EJ, Baldwin RL. Mammary amino acid utilization in dairy cows fed fat and its relationship to milk protein depression. J Dairy Sci. 1993;76:762–74. https://doi.org/10.3168/jds.S0022-0302(93)77400-7.
Wang B, Sun HZ, Xu NN, Zhu KJ, Liu JX. Amino acid utilization of lactating dairy cows when diets are changed from an alfalfa-based diet to cereal straw-based diets. Anim Feed Sci Technol. 2016;217:56–66. https://doi.org/10.1016/j.anifeedsci.2016.04.014.
Cai J, Zhao FQ, Liu JX, Wang DM. Local mammary glucose supply regulates availability and intracellular metabolic pathways of glucose in the mammary gland of lactating dairy goats under malnutrition of energy. Front Physiol. 2018;9:1467. https://doi.org/10.3389/fphys.2018.01467.
Balogh O, Szepes O, Kovacs K, Kulcsár-Huszenicza M, Reiczigel J, Alcazar J, et al. Interrelationships of growth hormone AluI polymorphism, insulin resistance, milk production and reproductive performance in Holstein-Friesian cows. Vet Med. 2008;53(11):604–16. https://doi.org/10.17221/1865-VETMED.
Pacheco-Rios D, Mackenzie DDS, McNabb WC. Comparison of two variants of the Fick principle for estimation of mammary blood flow in dairy cows fed two levels of dry matter intake. Can J Anim Sci. 2001;81:57–63. https://doi.org/10.4141/A00-035.
Chaiyabutr N. Control of mammary function during lactation in crossbred dairy cattle in the tropics. In: Chaiyabutr N, editor. Milk production – Advanced genetic traits, cellular mechanism, animal management and health. London: IntechOpen; 2012. Chapter 6. https://www.intechopen.com/chapters/39319.
Renaudeau D, Noblet J, Dourmad JY. Effect of ambient temperature on mammary gland metabolism in lactating sows. J Anim Sci. 2003;81:217–31. https://doi.org/10.2527/2003.811217x.
Choshniak I, McEwan-Jenkinson D, Blatchford DR, Peaker M. Blood flow and catecholamine concentration in bovine and caprine skin during thermal sweating. Comp Biochem Physiol C Comp Pharmacol. 1982;71(1):37–42. https://doi.org/10.1016/0306-4492(82)90007-7.
Dahl GE, Tao S, Laporta J. Heat stress impacts immune status in cows across the life cycle. Front Vet Sci. 2020;7:116. https://doi.org/10.3389/fvets.2020.00116.
Hu ZZ, Luo L, Lu Y, Cai J, Liu JX, Wang DM. Role of hypoxia in regulating mammary apoptosis-mediated lactation persistency alteration in high-yielding dairy cows. Anim Nutriomics. 2024;1:e3, 1–11. https://doi.org/10.1017/anr.2024.5.
Deussen A, Ohanyan V, Jannasch A, Yin L, Chilian W. Mechanisms of metabolic coronary flow regulation. J Mol Cell Cardiol. 2012;52:794–801. https://doi.org/10.1016/j.yjmcc.2011.10.001.
Cai J, Wang DM, Liu JX. Regulation of fluid flow through the mammary gland of dairy cows and its effect on milk production: a systematic review. J Sci Food Agric. 2018;98:1261–70. https://doi.org/10.1002/jsfa.8605.
Morris SM. Recent advances in arginine metabolism: roles and regulation of the arginases. Br J Pharmacol. 2009;157:922–30. https://doi.org/10.1111/j.1476-5381.2009.00278.x.
Cieslar SRL, Madsen TG, Purdie NG, Trout DR, Osborne VR, Cant JP. Mammary blood flow and metabolic activity are linked by a feedback mechanism involving nitric oxide synthesis. J Dairy Sci. 2014;97:2090–100. https://doi.org/10.3168/jds.2013-6961.
Trimm E, Red-Horse K. Vascular endothelial cell development and diversity. Nat Rev Cardiol. 2023;20:197–210. https://doi.org/10.1038/s41569-022-00770-1.
Madsen TG, Cieslar SRL, Trout DR, Nielsen MO, Cant JP. Inhibition of local blood flow control systems in the mammary glands of lactating cows affects uptakes of energy metabolites from blood. J Dairy Sci. 2015;98:3046–58. https://doi.org/10.3168/jds.2014-8200.
Curtis RV, Kim JJM, Bajramaj DL, Doelman J, Osborne VR, Cant JP. Decline in mammary translational capacity during intravenous glucose infusion into lactating dairy cows. J Dairy Sci. 2014;97:430–8. https://doi.org/10.3168/jds.2013-7252.
Youngblood JP, VandenBrooks JM, Babarinde O, Donnay ME, Elliott DB, Fredette-Roman J, et al. Oxygen supply limits the chronic heat tolerance of locusts during the first instar only. J Insect Physiol. 2020;127: 104157. https://doi.org/10.1016/j.jinsphys.2020.104157.
Serano M, Pietrangelo L, Paolini C, Guarnier FA, Protasi F. Oxygen consumption and basal metabolic rate as markers of susceptibility to malignant hyperthermia and heat stroke. Cells. 2022;11:2468. https://doi.org/10.3390/cells11162468.
Wang Y, Venton BJ. Caffeine modulates spontaneous adenosine and oxygen changes during ischemia and reperfusion. ACS Chem Neurosci. 2019;10:1941–9. https://doi.org/10.1021/acschemneuro.8b00251.
Zhao FQ. Biology of glucose transport in the mammary gland. J Mammary Gland Biol Neoplasia. 2014;19:3–17. https://doi.org/10.1007/s10911-013-9310-8.
Shao Y, Wellman TL, Lounsbury KM, Zhao FQ. Differential regulation of GLUT1 and GLUT8 expression by hypoxia in mammary epithelial cells. Am J Physiol Regul Integr Comp Physiol. 2014;307:R237–247. https://doi.org/10.1152/ajpregu.00093.2014.
Sadovnikova A, Garcia SC, Hovey RC. A comparative review of the cell biology, biochemistry, and genetics of lactose synthesis. J Mammary Gland Biol Neoplasia. 2021;26:181–96. https://doi.org/10.1007/s10911-021-09490-7.
Guinard-Flament J, Delamaire E, Lemosquet S, Boutinaud M, David Y. Changes in mammary uptake and metabolic fate of glucose with once-daily milking and feed restriction in dairy cows. Reprod Nutr Dev. 2006;46:589–98. https://doi.org/10.1051/rnd:2006030.
Gao ST, Ma L, Zhou Z, Zhou ZK, Baumgard LH, Jiang D, et al. Heat stress negatively affects the transcriptome related to overall metabolism and milk protein synthesis in mammary tissue of midlactating dairy cows. Physiol Genomics. 2019;51:400–9. https://doi.org/10.1152/physiolgenomics.00039.2019.
Abbas Z, Sammad A, Hu L, Fang H, Xu Q, Wang Y. Glucose metabolism and dynamics of facilitative glucose transporters (GLUTs) under the influence of heat stress in dairy cattle. Metabolites. 2020;10:312. https://doi.org/10.3390/metabo10080312.
Galster AD, Clutter WE, Cryer PE, Collins JA, Bier DM. Epinephrine plasma thresholds for lipolytic effects in man: measurements of fatty acid transport with [l-13C]palmitic acid. J Clin Invest. 1981;67:1729–38. https://doi.org/10.1172/jci110211.
Sammad A, Wang YJ, Umer S, Lirong H, Khan I, Khan A, et al. Nutritional physiology and biochemistry of dairy cattle under the influence of heat stress: consequences and opportunities. Animals. 2020;10:793. https://doi.org/10.3390/ani10050793.
Min L, Cheng JB, Shi BL, Yang HJ, Zheng N, Wang JQ. Effects of heat stress on serum insulin, adipokines, AMP-activated protein kinase, and heat shock signal molecules in dairy cows. J Zhejiang Univ-Sci B (Biomed & Biotechnol). 2015;16:541–8. https://doi.org/10.1631/jzus.B1400341.
Itoh F, Obara Y, Fuse H, Rose MT, Osaka I, Takahashi H. Effects of heat exposure on plasma insulin, glucagon and metabolites in response to nutrient injection in heifers. Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1998;119:157–64. https://doi.org/10.1016/s0742-8413(97)00203-x.
Tian H, Zheng N, Wang WL, Cheng JB, Li SL, Zhang Y, et al. Integrated metabolomics study of the milk of heat-stressed lactating dairy cows. Sci Rep. 2016;6:24208. https://doi.org/10.1038/srep24208.
Chiang SK, Chen SE, Chang LC. The role of HO-1 and its crosstalk with oxidative stress in cancer cell survival. Cells. 2021;10:2401. https://doi.org/10.3390/cells10092401.
Wang YR, Yang CX, Elsheikh NAH, Li CM, Yang FX, Wang GL, et al. HO-1 reduces heat stress-induced apoptosis in bovine granulosa cells by suppressing oxidative stress. Aging. 2019;11(15):5535–47. https://doi.org/10.18632/aging.102136.
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