Longitudinal genomic analyses of automatically-recorded vaginal temperature in lactating sows under heat stress conditions based on random regression models.
Journal
Genetics, selection, evolution : GSE
ISSN: 1297-9686
Titre abrégé: Genet Sel Evol
Pays: France
ID NLM: 9114088
Informations de publication
Date de publication:
21 Dec 2023
21 Dec 2023
Historique:
received:
28
04
2023
accepted:
12
12
2023
medline:
22
12
2023
pubmed:
22
12
2023
entrez:
22
12
2023
Statut:
epublish
Résumé
Automatic and continuous recording of vaginal temperature (T Heritability estimates for T T
Sections du résumé
BACKGROUND
BACKGROUND
Automatic and continuous recording of vaginal temperature (T
RESULTS
RESULTS
Heritability estimates for T
CONCLUSIONS
CONCLUSIONS
T
Identifiants
pubmed: 38129768
doi: 10.1186/s12711-023-00868-1
pii: 10.1186/s12711-023-00868-1
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
95Subventions
Organisme : National Institute of Food and Agriculture
ID : 2020-67015-31575
Organisme : National Institute of Food and Agriculture
ID : 2022-67021-37022
Informations de copyright
© 2023. The Author(s).
Références
Morrison SR. Ruminant heat stress: effect on production and means of alleviation. J Anim Sci. 1983;57:1594–600.
pubmed: 6370944
doi: 10.2527/jas1983.5761594x
West JW. Effects of heat-stress on production in dairy cattle. J Dairy Sci. 2003;86:2131–44.
pubmed: 12836950
doi: 10.3168/jds.S0022-0302(03)73803-X
Wolfenson D, Roth Z. Impact of heat stress on cow reproduction and fertility. Anim Front. 2018;9:32–8.
pubmed: 32002237
pmcid: 6951943
doi: 10.1093/af/vfy027
Polsky L, von Keyserlingk MAG. Invited review: effects of heat stress on dairy cattle welfare. J Dairy Sci. 2017;100:8645–57.
pubmed: 28918147
doi: 10.3168/jds.2017-12651
Cabezón FA, Schinckel PASAP, Richert BT, Peralta WA, Gandarillas M. Technical note: application of models to estimate daily heat production of lactating sows. Prof Anim Sci. 2017;33:357–62.
doi: 10.15232/pas.2016-01583
Luo H, Brito LF, Li X, Su G, Dou J, Xu W, et al. Genetic parameters for rectal temperature, respiration rate, and drooling score in Holstein cattle and their relationships with various fertility, production, body conformation, and health traits. J Dairy Sci. 2021;104:4390–403.
pubmed: 33685707
doi: 10.3168/jds.2020-19192
Luo H, Hu L, Brito LF, Dou J, Sammad A, Chang Y, et al. Weighted single-step GWAS and RNA sequencing reveals key candidate genes associated with physiological indicators of heat stress in Holstein cattle. J Anim Sci Biotechnol. 2022;13:108.
pubmed: 35986427
pmcid: 9392250
doi: 10.1186/s40104-022-00748-6
Freitas PHF, Wang Y, Yan P, Oliveira HR, Schenkel FS, Zhang Y, et al. Genetic diversity and signatures of selection for thermal stress in cattle and other two Bos species adapted to divergent climatic conditions. Front Genet. 2021;12: 604823.
pubmed: 33613634
pmcid: 7887320
doi: 10.3389/fgene.2021.604823
Freitas PHF, Johnson JS, Chen S, Oliveira HR, Tiezzi F, Lázaro SF, et al. Definition of environmental variables and critical periods to evaluate heat tolerance in large white pigs based on single-step genomic reaction norms. Front Genet. 2021;12: 717409.
pubmed: 34887897
pmcid: 8650309
doi: 10.3389/fgene.2021.717409
Hu L, Sammad A, Zhang C, Brito LF, Xu Q, Wang Y. Transcriptome analyses reveal essential roles of alternative splicing regulation in heat-stressed Holstein cows. Int J Mol Sci. 2022;23:10664.
pubmed: 36142577
pmcid: 9505234
doi: 10.3390/ijms231810664
Fu Y, Hu J, Cheng H. Research note: Probiotic, Bacillus subtilis, alleviates neuroinflammation in the hippocampus via the gut microbiota-brain axis in heat-stressed chickens. Poult Sci. 2023;102: 102635.
pubmed: 37011470
pmcid: 10240367
doi: 10.1016/j.psj.2023.102635
Luo H, Li X, Hu L, Xu W, Chu Q, Liu A, et al. Genomic analyses and biological validation of candidate genes for rectal temperature as an indicator of heat stress in Holstein cattle. J Dairy Sci. 2021;104:4441–51.
pubmed: 33589260
doi: 10.3168/jds.2020-18725
Lee WC, Wen HC, Chang CP, Chen MY, Lin MT. Heat shock protein 72 overexpression protects against hyperthermia, circulatory shock, and cerebral ischemia during heatstroke. J Appl Physiol. 2006;100:2073–82.
pubmed: 16627676
doi: 10.1152/japplphysiol.01433.2005
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;92:1986–97.
pubmed: 19389956
doi: 10.3168/jds.2008-1641
Vickers LA, Burfeind O, von Keyserlingk MAG, Veira DM, Weary DM, Heuwieser W. Technical note: comparison of rectal and vaginal temperatures in lactating dairy cows. J Dairy Sci. 2010;93:5246–51.
pubmed: 20965340
doi: 10.3168/jds.2010-3388
Collier RJ, Dahl GE, VanBaale MJ. Major advances associated with environmental effects on dairy cattle. J Dairy Sci. 2006;89:1244–53.
pubmed: 16537957
doi: 10.3168/jds.S0022-0302(06)72193-2
Coppock CE, Grant PA, Portzer SJ, Charles DA, Escobosa A. Lactating dairy cow responses to dietary sodium, chloride, and bicarbonate during hot weather. J Dairy Sci. 1982;65:566–76.
pubmed: 6284822
doi: 10.3168/jds.S0022-0302(82)82234-0
Schaeffer LR. Application of random regression models in animal breeding. Livest Prod Sci. 2004;86:35–45.
doi: 10.1016/S0301-6226(03)00151-9
Oliveira HR, Brito LF, Lourenco DAL, Silva FF, Jamrozik J, Schaeffer LR, et al. Invited review: advances and applications of random regression models: from quantitative genetics to genomics. J Dairy Sci. 2019;102:7664–83.
pubmed: 31255270
doi: 10.3168/jds.2019-16265
Meyer K. Random regression analyses using B-splines to model growth of Australian Angus cattle. Genet Sel Evol. 2005;37:473–500.
pubmed: 16093011
pmcid: 2697221
doi: 10.1186/1297-9686-37-6-473
Siddiqui SH, Kang D, Park J, Khan M, Shim K. Chronic heat stress regulates the relation between heat shock protein and immunity in broiler small intestine. Sci Rep. 2020;10:18872.
pubmed: 33139769
pmcid: 7608671
doi: 10.1038/s41598-020-75885-x
Jovic K, Sterken MG, Grilli J, Bevers RPJ, Rodriguez M, Riksen JAG, et al. Temporal dynamics of gene expression in heat-stressed Caenorhabditis elegans. PLoS One. 2017;12:e0189445.
pubmed: 29228038
pmcid: 5724892
doi: 10.1371/journal.pone.0189445
Oliveira HR, Cant JP, Brito LF, Feitosa FLB, Chud TCS, Fonseca PAS, et al. Genome-wide association for milk production traits and somatic cell score in different lactation stages of Ayrshire, Holstein, and Jersey dairy cattle. J Dairy Sci. 2019;102:8159–74.
pubmed: 31301836
doi: 10.3168/jds.2019-16451
Johnson J, Wen H, Freitas PHF, Maskal J, Hartman S, Byrd M, et al. Evaluating phenotypes associated with heat tolerance and identifying moderate and severe heat stress thresholds in lactating sows housed in mechanically or naturally ventilated barns during the summer under commercial conditions. J Anim Sci. 2023;101:skad129.
pubmed: 37104047
pmcid: 10195204
doi: 10.1093/jas/skad129
Burrow HM. Importance of adaptation and genotype × environment interactions in tropical beef breeding systems. Animal. 2012;6:729–40.
pubmed: 22558921
doi: 10.1017/S175173111200002X
Misztal I, Tsuruta S, Luorenco DA, Masuda Y, Aguilar I, Legarra A, et al. Manual for BLUPF90 family programs. University of Georgia; 2018. http://nce.ads.uga.edu/wiki/lib/exe/fetch.php?media=blupf90_all8.pdf/ . Accessed 10 Oct 2023.
VanRaden PM. Efficient methods to compute genomic predictions. J Dairy Sci. 2008;91:4414–23.
pubmed: 18946147
doi: 10.3168/jds.2007-0980
Schaeffer LR, Jamrozik J. Random regression models: a longitudinal perspective. J Anim Breed Genet. 2008;124:145–6.
doi: 10.1111/j.1439-0388.2008.00748.x
Kirkpatrick M, Lofsvold D, Bulmer M. Analysis of the inheritance, selection and evolution of growth trajectories. Genetics. 1990;124:979–93.
pubmed: 2323560
pmcid: 1203988
doi: 10.1093/genetics/124.4.979
Buck AL. New equations for computing vapor pressure and enhancement factor. J Appl Meteorol Climatol. 1981;20:1527–32.
doi: 10.1175/1520-0450(1981)020<1527:NEFCVP>2.0.CO;2
Silva FF, Mulder HA, Knol EF, Lopes MS, Guimarães SEF, Lopes PS, et al. Sire evaluation for total number born in pigs using a genomic reaction norms approach. J Anim Sci. 2014;92:3825–34.
pubmed: 24492557
doi: 10.2527/jas.2013-6486
Akaike H. A new look at the statistical model identification. IEEE Trans Autom Control. 1974;19:716–23.
doi: 10.1109/TAC.1974.1100705
Ovenden B, Milgate A, Wade LJ, Rebetzke GJ, Holland JB. Accounting for genotype-by-environment interactions and residual genetic variation in genomic selection for water-soluble carbohydrate concentration in wheat. G3 (Bethesda). 2018;8:1909–19.
pubmed: 29661842
pmcid: 5982820
doi: 10.1534/g3.118.200038
Lozada-Soto EA, Maltecca C, Wackel H, Flowers W, Gray K, He Y, et al. Evidence for recombination variability in purebred swine populations. J Anim Breed Genet. 2021;138:259–73.
pubmed: 32975329
doi: 10.1111/jbg.12510
de Fragomeni O, Misztal I, Lourenco DL, Aguilar I, Okimoto R, Muir WM. Changes in variance explained by top SNP windows over generations for three traits in broiler chicken. Front Genet. 2014;5:332.
pubmed: 25324857
pmcid: 4181244
doi: 10.3389/fgene.2014.00332
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, et al. Gene ontology: tool for the unification of biology. Nat Genet. 2000;25:25–9.
pubmed: 10802651
pmcid: 3037419
doi: 10.1038/75556
Kanehisa M, Goto S. KEGG: Kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 2000;28:27–30.
pubmed: 10592173
pmcid: 102409
doi: 10.1093/nar/28.1.27
Yu G, Wang LG, Han Y, He QY. clusterProfiler: an R package for comparing biological themes among gene clusters. OMICS. 2012;16:284–7.
pubmed: 22455463
pmcid: 3339379
doi: 10.1089/omi.2011.0118
Boligon AA, Mercadante MEZ, Lôbo RB, Baldi F, Albuquerque LG. Random regression analyses using B-spline functions to model growth of Nellore cattle. Animal. 2012;6:212–20.
pubmed: 22436178
doi: 10.1017/S1751731111001534
Baldi F, Alencar MM, Albuquerque LG. Random regression analyses using B-splines functions to model growth from birth to adult age in Canchim cattle. J Anim Breed Genet. 2010;127:433–41.
pubmed: 21077967
doi: 10.1111/j.1439-0388.2010.00873.x
Dikmen S, Cole JB, Null DJ, Hansen PJ. Heritability of rectal temperature and genetic correlations with production and reproduction traits in dairy cattle. J Dairy Sci. 2012;95:3401–5.
pubmed: 22612974
doi: 10.3168/jds.2011-4306
Seath DM. Heritability of heat tolerance in dairy cattle. J Dairy Sci. 1947;30:137–44.
doi: 10.3168/jds.S0022-0302(47)92331-X
Tan CL, Knight ZA. Regulation of body temperature by the nervous system. Neuron. 2018;98:31–48.
pubmed: 29621489
pmcid: 6034117
doi: 10.1016/j.neuron.2018.02.022
Burrow HM. Variances and covariances between productive and adaptive traits and temperament in a composite breed of tropical beef cattle. Livest Prod Sci. 2001;70:213–33.
doi: 10.1016/S0301-6226(01)00178-6
Gourdine J-L, Mandonnet N, Giorgi M, Renaudeau D. Genetic parameters for thermoregulation and production traits in lactating sows reared in tropical climate. Animal. 2017;11:365–74.
pubmed: 27378416
doi: 10.1017/S175173111600135X
Silpa MV, König S, Sejian V, Malik PK, Nair MRR, Fonseca VFC, et al. Climate-resilient dairy cattle production: applications of genomic tools and statistical models. Front Vet Sci. 2021;8: 625189.
pubmed: 33996959
pmcid: 8117237
doi: 10.3389/fvets.2021.625189
Bernabucci U, Lacetera N, Baumgard LH, Rhoads RP, Ronchi B, Nardone A. Metabolic and hormonal acclimation to heat stress in domesticated ruminants. Animal. 2010;4:1167–83.
pubmed: 22444615
doi: 10.1017/S175173111000090X
George WD, Godfrey RW, Ketring RC, Vinson MC, Willard ST. Relationship among eye and muzzle temperatures measured using digital infrared thermal imaging and vaginal and rectal temperatures in hair sheep and cattle. J Anim Sci. 2014;92:4949–55.
pubmed: 25253816
doi: 10.2527/jas.2014-8087
Sellier N, Guettier E, Staub C. A review of methods to measure animal body temperature in precision farming. Am J Agric Sc Technol. 2014;2:74–99.
Stiehler T, Heuwieser W, Pfützner A, Burfeind O. The course of rectal and vaginal temperature in early postpartum sows. J Swine Health Prod. 2015;23:72–83.
Chauhan SS, Rashamol VP, Bagath M, Sejian V, Dunshea FR. Impacts of heat stress on immune responses and oxidative stress in farm animals and nutritional strategies for amelioration. Int J Biometeorol. 2021;65:1231–44.
pubmed: 33496873
doi: 10.1007/s00484-021-02083-3
Steele M. Does heat stress affect immune function in dairy cows? Vet Evid. 2016. https://doi.org/10.18849/ve.v1i3.39 .
doi: 10.18849/ve.v1i3.39
Safa S, Kargar S, Moghaddam GA, Ciliberti MG, Caroprese M. Heat stress abatement during the postpartum period: effects on whole lactation milk yield, indicators of metabolic status, inflammatory cytokines, and biomarkers of the oxidative stress. J Anim Sci. 2019;97:122–32.
pubmed: 30346551
doi: 10.1093/jas/sky408
Ju XH, Xu HJ, Yong YH, An LL, Jiao PR, Liao M. Heat stress upregulation of Toll-like receptors 2/4 and acute inflammatory cytokines in peripheral blood mononuclear cell (PBMC) of Bama miniature pigs: an in vivo and in vitro study. Animal. 2014;8:1462–8.
pubmed: 24912383
doi: 10.1017/S1751731114001268
Xiang-hong J, Yan-hong Y, Han-jin X, Li-long A, Yingmei X. Impacts of heat stress on baseline immune measures and a subset of T cells in Bama miniature pigs. Livest Sci. 2011;135:289–92.
doi: 10.1016/j.livsci.2010.07.009
Wojtas K, Cwynar P, Kołacz R. Effect of thermal stress on physiological and blood parameters in merino sheep. B Vet I Pulawy. 2014;58:283–8.
doi: 10.2478/bvip-2014-0043
da Silva GR, da Costa MJ, Sobrinho AG. Influence of hot environments on some blood variables of sheep. Int J Biometeorol. 1992;36:223–5.
pubmed: 1428224
doi: 10.1007/BF02726402
Madhusoodan AP, Sejian V, Afsal A, Bagath M, Krishnan G, Savitha ST, et al. Differential expression patterns of candidate genes pertaining to productive and immune functions in hepatic tissue of heat-stressed Salem Black goats. Biol Rhythm Res. 2021;52:809–20.
doi: 10.1080/09291016.2019.1607213
Paul A, Dangi SS, Gupta M, Singh J, Thakur N, Naskar S, et al. Expression of TLR genes in Black Bengal goat (Capra hircus) during different seasons. Small Ruminant Res. 2015;124:17–23.
doi: 10.1016/j.smallrumres.2015.01.011
Hirakawa R, Nurjanah S, Furukawa K, Murai A, Kikusato M, Nochi T, et al. Heat stress causes immune abnormalities via massive damage to effect proliferation and differentiation of lymphocytes in broiler chickens. Front Vet Sci. 2020;7:46.
pubmed: 32118068
pmcid: 7020782
doi: 10.3389/fvets.2020.00046
Bartlett JR, Smith MO. Effects of different levels of zinc on the performance and immunocompetence of broilers under heat stress. Poult Sci. 2003;82:1580–8.
pubmed: 14601736
doi: 10.1093/ps/82.10.1580
Mehla K, Magotra A, Choudhary J, Singh AK, Mohanty AK, Upadhyay RC, et al. Genome-wide analysis of the heat stress response in Zebu (Sahiwal) cattle. Gene. 2014;533:500–7.
pubmed: 24080481
doi: 10.1016/j.gene.2013.09.051
Rowell LB, Brengelmann GL, Murray JA. Cardiovascular responses to sustained high skin temperature in resting man. J Appl Physiol. 1969;27:673–80.
pubmed: 5360442
doi: 10.1152/jappl.1969.27.5.673
Low DA, Keller DM, Wingo JE, Brothers RM, Crandall CG. Sympathetic nerve activity and whole body heat stress in humans. J Appl Physiol. 2011;111:1329–34.
pubmed: 21868685
pmcid: 3220304
doi: 10.1152/japplphysiol.00498.2011
Crandall CG, Wilson TE, Marving J, Vogelsang TW, Kjaer A, Hesse B, et al. Effects of passive heating on central blood volume and ventricular dimensions in humans: heat stress and regional blood volume distribution. J Physiol. 2008;586:293–301.
pubmed: 17962331
doi: 10.1113/jphysiol.2007.143057
He BJ, Zhao D, Dong X, Zhao Z, Li L, Duo L, et al. Will individuals visit hospitals when suffering heat-related illnesses? Yes, but…. Build Environ. 2022;208: 108587.
doi: 10.1016/j.buildenv.2021.108587
Kenny GP, Yardley J, Brown C, Sigal RJ, Jay O. Heat stress in older individuals and patients with common chronic diseases. Can Med Assoc J. 2010;182:1053–60.
doi: 10.1503/cmaj.081050
Crandall CG, Wilson TE. Human cardiovascular responses to passive heat stress. In: Terjung R, editor. Comprehensive physiology. Hoboken: Wiley; 2014. p. 17–43.
doi: 10.1002/cphy.c140015
Booth RE, Johnson JP, Stockand JD. Aldosterone. Adv Physiol Educ. 2002;26:8–20.
pubmed: 11850323
doi: 10.1152/advan.00051.2001
El-Nouty FD, Elbanna IM, Davis TP, Johnson HD. Aldosterone and ADH response to heat and dehydration in cattle. J Appl Physiol Respir Environ Exerc Physiol. 1980;48:249–55.
pubmed: 7364609
Etches RJ, John T, Gibbins A. Behavioural, physiological, neuroendocrine and molecular responses to heat stress. In: Daghir NJ, editor. Poultry production in hot climates. 2nd ed. Wallingford: CAB International; 2008. p. 48–79.
doi: 10.1079/9781845932589.0048
Tao S, Dahl GE. Invited review: heat stress effects during late gestation on dry cows and their calves. J Dairy Sci. 2013;96:4079–93.
pubmed: 23664343
doi: 10.3168/jds.2012-6278
Palikaras K, Lionaki E, Tavernarakis N. Balancing mitochondrial biogenesis and mitophagy to maintain energy metabolism homeostasis. Cell Death Differ. 2015;22:1399–401.
pubmed: 26256515
pmcid: 4532782
doi: 10.1038/cdd.2015.86
Palikaras K, Lionaki E, Tavernarakis N. Coupling mitogenesis and mitophagy for longevity. Autophagy. 2015;11:1428–30.
pubmed: 26083448
pmcid: 4590656
doi: 10.1080/15548627.2015.1061172
Tamura Y, Kitaoka Y, Matsunaga Y, Hoshino D, Hatta H. Daily heat stress treatment rescues denervation-activated mitochondrial clearance and atrophy in skeletal muscle. J Physiol. 2015;593:2707–20.
pubmed: 25900738
pmcid: 4500354
doi: 10.1113/JP270093
Brownstein AJ, Ganesan S, Summers CM, Pearce S, Hale BJ, Ross JW, et al. Heat stress causes dysfunctional autophagy in oxidative skeletal muscle. Physiol Rep. 2017;5: e13317.
pubmed: 28646096
pmcid: 5492206
doi: 10.14814/phy2.13317
Popoli M, Yan Z, McEwen BS, Sanacora G. The stressed synapse: the impact of stress and glucocorticoids on glutamate transmission. Nat Rev Neurosci. 2012;13:22–37.
doi: 10.1038/nrn3138
Asea AAA, Brown IR. Heat shock proteins and the brain: implications for neurodegenrative diseases and neuroprotection. Dordrecht: Springer; 2008.
doi: 10.1007/978-1-4020-8231-3
Kiang J, Tsokos GC. Heat Shock Protein 70 kDa: molecular biology, biochemistry, and physiology. Pharmacol Ther. 1998;80:183–201.
pubmed: 9839771
doi: 10.1016/S0163-7258(98)00028-X
Cheruiyot EK, Haile-Mariam M, Cocks BG, MacLeod IM, Xiang R, Pryce JE. New loci and neuronal pathways for resilience to heat stress in cattle. Sci Rep. 2021;11:16619.
pubmed: 34404823
pmcid: 8371109
doi: 10.1038/s41598-021-95816-8
Gilbert SS, van den Heuvel CJ, Ferguson SA, Dawson D. Thermoregulation as a sleep signalling system. Sleep Med Rev. 2004;8:81–93.
pubmed: 15033148
doi: 10.1016/S1087-0792(03)00023-6
Van Someren EJW. Mechanisms and functions of coupling between sleep and temperature rhythms. Prog Brain Res. 2006;153:309–24.
pubmed: 16876583
doi: 10.1016/S0079-6123(06)53018-3
Li Y, Feng X, Wang H, Meng C, Zhang J, Qian Y, et al. Transcriptome analysis reveals corresponding genes and key pathways involved in heat stress in Hu sheep. Cell Stress Chaperones. 2019;24:1045–54.
pubmed: 31428918
pmcid: 6882975
doi: 10.1007/s12192-019-01019-6
Calapre L, Gray ES, Ziman M. Heat stress: a risk factor for skin carcinogenesis. Cancer Lett. 2013;337:35–40.
pubmed: 23748013
doi: 10.1016/j.canlet.2013.05.039
Srikanth K, Kwon A, Lee E, Chung H. Characterization of genes and pathways that respond to heat stress in Holstein calves through transcriptome analysis. Cell Stress Chaperones. 2017;22:29–42.
pubmed: 27848120
doi: 10.1007/s12192-016-0739-8
Tomaschitz A, Pilz S, Ritz E, Meinitzer A, Boehm BO, Marz W. Plasma aldosterone levels are associated with increased cardiovascular mortality: the Ludwigshafen Risk and Cardiovascular Health (LURIC) study. Eur Heart J. 2010;31:1237–47.
pubmed: 20200015
doi: 10.1093/eurheartj/ehq019
Machado NLS, Abbott SBG, Resch JM, Zhu L, Arrigoni E, Lowell BB, et al. A glutamatergic hypothalamomedullary circuit mediates thermogenesis, but not heat conservation, during stress-induced hyperthermia. Curr Biol. 2018;28:2291-2301.e5.
pubmed: 30017482
pmcid: 6085892
doi: 10.1016/j.cub.2018.05.064
McNab BK. The physiological ecology of vertebrates. Ithaca: Cornell University Press; 2002.
Pan D. The hippo signaling pathway in development and cancer. Dev Cell. 2010;19:491–505.
pubmed: 20951342
pmcid: 3124840
doi: 10.1016/j.devcel.2010.09.011
Jimenez RH, Lee JS, Francesconi M, Castellani G, Neretti N, Sanders JA, et al. Regulation of gene expression in hepatic cells by the mammalian target of rapamycin (mTOR). PLoS One. 2010;5:e9084.
pubmed: 20140209
pmcid: 2816708
doi: 10.1371/journal.pone.0009084
Das A, Rushton PJ, Rohila JS. Metabolomic profiling of soybeans (Glycine max L.) reveals the importance of sugar and nitrogen metabolism under drought and heat stress. Plants (Basel). 2017;6:21.
pubmed: 28587097
pmcid: 5489793
doi: 10.3390/plants6020021
Stasolla C, Loukanina N, Yeung EC, Thorpe TA. Alterations in pyrimidine nucleotide metabolism as an early signal during the execution of programmed cell death in tobacco BY-2 cells. J Exp Bot. 2004;55:2513–22.
pubmed: 15361531
doi: 10.1093/jxb/erh259
Ray PD, Huang B-W, Tsuji Y. Reactive oxygen species (ROS) homeostasis and redox regulation in cellular signaling. Cell Signal. 2012;24:981–90.
pubmed: 22286106
pmcid: 3454471
doi: 10.1016/j.cellsig.2012.01.008
Gu Z, Li L, Tang S, Liu C, Fu X, Shi Z, et al. Metabolomics reveals that crossbred dairy buffaloes are more thermotolerant than Holstein cows under chronic heat stress. J Agric Food Chem. 2018;66:12889–97.
pubmed: 30472851
doi: 10.1021/acs.jafc.8b02862
Liao Y, Hu R, Wang Z, Peng Q, Dong X, Zhang X, et al. Metabolomics profiling of serum and urine in three beef cattle breeds revealed different levels of tolerance to heat stress. J Agric Food Chem. 2018;66:6926–35.
pubmed: 29905066
doi: 10.1021/acs.jafc.8b01794
Contreras-Jodar A, Salama AA, Hamzaoui S, Vailati-Riboni M, Caja G, Loor JJ. Effects of chronic heat stress on lactational performance and the transcriptomic profile of blood cells in lactating dairy goats. J Dairy Res. 2018;85:423–30.
pubmed: 30236165
doi: 10.1017/S0022029918000705
Kosunen KJ, Pakarinen AJ, Kuoppasalmi K, Adlercreutz H. Plasma renin activity, angiotensin II, and aldosterone during intense heat stress. J Appl Physiol. 1976;41:323–7.
pubmed: 965299
doi: 10.1152/jappl.1976.41.3.323
Fan GC. Role of heat shock proteins in stem cell behavior. Prog Mol Biol Transl Sci. 2012;111:305–22.
pubmed: 22917237
pmcid: 4422174
doi: 10.1016/B978-0-12-398459-3.00014-9
Baumgard LH, Rhoads RP Jr. Effects of heat stress on postabsorptive metabolism and energetics. Annu Rev Anim Biosci. 2013;1:311–37.
pubmed: 25387022
doi: 10.1146/annurev-animal-031412-103644
Yin C, Tang S, Liu L, Cao A, Xie J, Zhang H. Effects of bile acids on growth performance and lipid metabolism during chronic heat stress in broiler chickens. Animals (Basel). 2021;11:630.
pubmed: 33673472
doi: 10.3390/ani11030630
Kim JM, Lim KS, Byun M, Lee KT, Yang Y, Park M, et al. Identification of the acclimation genes in transcriptomic responses to heat stress of White Pekin duck. Cell Stress Chaperones. 2017;22:787–97.
pubmed: 28634817
pmcid: 5655367
doi: 10.1007/s12192-017-0809-6
Hansen A, Bi P, Nitschke M, Ryan P, Pisaniello D, Tucker G. The effect of heat waves on mental health in a temperate Australian city. Environ Health Perspect. 2008;116:1369–75.
pubmed: 18941580
pmcid: 2569097
doi: 10.1289/ehp.11339
Berry HL, Bowen K, Kjellstrom T. Climate change and mental health: a causal pathways framework. Int J Public Health. 2010;55:123–32.
pubmed: 20033251
doi: 10.1007/s00038-009-0112-0
Ma Y, Bao Y, Wang S, Li T, Chang X, Yang G, et al. Anti-inflammation effects and potential mechanism of saikosaponins by regulating nicotinate and nicotinamide metabolism and arachidonic acid metabolism. Inflammation. 2016;39:1453–61.
pubmed: 27251379
doi: 10.1007/s10753-016-0377-4
Tribble JR, Otmani A, Sun S, Ellis SA, Cimaglia G, Vohra R, et al. Nicotinamide provides neuroprotection in glaucoma by protecting against mitochondrial and metabolic dysfunction. Redox Biol. 2021;43: 101988.
pubmed: 33932867
pmcid: 8103000
doi: 10.1016/j.redox.2021.101988