PLANT BIOLOGY
ANIMAL BIOLOGY
SUBSCRIPTION
E-SUBSCRIPTION
 
MAP
MAIN PAGE

 

 

 

 

doi: 10.15389/agrobiology.2025.6.986eng

UDC: 636.2:636.082.2:577.2

Acknowledgements:
Supported financially from the Russian Science Foundation, project No. 19-76-20012.

 

SEARCH FOR SELECTION SIGNATURES IN GENOMES OF NORTHERN AND STEPPE MODERN CATTLE IN RUSSIA AS COMPARED TO SAMPLES OF XIX-XX CENTURIES

A.S. Abdelmanova , T.E. Deniskova, A.V. Shakhin, A.A. Nikolaev,
G.O. Abramov, O.I. Boronetskaya, V.A. Bagirov, V.I. Truchachev,
N.A. Zinovieva

Ernst Federal Research Center for Animal Husbandry, 60, pos. Dubrovitsy, Podolsk District, Moscow Province, 142132 Russia, e-mail abdelmanova@vij.ru (✉ corresponding author) horarka@yandex.ru, alexshakhin@vij.ru,
alexandralces@yandex.ru, g0work@mail.ru, liskun@rgau-msha.ru, vugarbagirov@mail.ru, rector@rgau-msha.ru,
n_zinovieva@mail.ru

ORCID:
Abdelmanova A.S. orcid.org/0000-0003-4752-0727
Boronetskaya O.I. orcid.org/0000-0001-8389-5572
Deniskova T.E. orcid.org/0000-0002-5809-1262
Bagirov V.A. orcid.org/0000-0001-5398-8815
Shakhin A.V. orcid.org/0000-0003-4959-878X
Truchachev V.I. orcid.org/0000-0003-4676-5407
Nikolaev A.A. orcid.org/0000-0001-9355-3285
Zinovieva N.A. orcid.org/0000-0003-4017-6863
Abramov G.O. orcid.org/0009-0000-7239-3227

Final revision received May 29, 2025
Accepted July 22, 2025

The development of whole genome sequencing (WGS) technology opens new opportunities in studying the genomic variability of farm animals under the influence of natural and artificial selection. Analysis of WGS data allows us to identify key genes and genomic regions responsible for the formation of adaptive properties to specific natural and climatic breeding conditions. Selection and genetic drift are key sources of genetic differentiation between representatives of original and modern breeds. Studying the dynamics of changes in the gene pool of local breeds is relevant, since local breeds are carriers of rare and valuable genetic variants that may become a priority in the event of changing market demands and climate change. This paper describes for the first time the results of identifying genomic regions fixed as a result of selection in contrasting groups of cattle adapted to significantly different environmental conditions, and provides a structural and functional annotation of the genes localized in them. Genes common to modern and ancestral cattle populations of the studied groups were identified. The aim of the study was to compare the genomes of historical and modern cattle of different breeds based on WGS data to identifygenomic regions affected by natural and artificial selection. The study material included museum cattle skull specimens from the E.F. Liskun Livestock Museum (Timiryazev Russian State Agrarian University - Moscow Agricultural Academy, Moscow), dating from the late 19th to early 20th centuries, as well as samples from breeding animals stored in the biological collection of the National Center for Farm Animal Genetic Resources of the L.K. Ernst Federal Research Center for Animal Husbandry. The northern cattle group was represented by samples of the Kholmogor and Yaroslavl breeds, and the steppe cattle group was represented by samples of Kalmyk cattle. The sample of historical specimens (n = 20)included 15 samples of northern cattle (Kholmogor cattle, n = 8; Yaroslavl cattle, n = 7) and 5 samples of steppe (Kalmyk) cattle. The sample of modern specimens included 17, 11 and12 samples of the above-mentioned breeds, respectively. The final data set included the genotypes for 1,615,259 SNPs. DNA extraction from museum specimens was performed using the previously described method, and from modern specimens, using the DNA-Extran 2 kit (Sintol JSC, Moscow). Libraries for whole-genome sequencing using NGS technology were prepared using the TruSeq DNA Nano Library Prep kit (Illumina, Inc., USA) and the Accel-NGS® 2S Plus DNA Library Kit (IDT). Sequencing was performed on a NovaSeq 6000 sequencer (2.5150 bp). Three methods were used to identify genomic regions under selection pressure: pairwise comparison of populations based on FST genetic distances usinga sliding window, analysis of cross-population extended haplotype homozygosity (XP-EHH), and identification of regions of excess homozygosity (ROH islands). The absence of overlapping genomic regions under selection pressure in the genome of the historical and modern populations of studied cattle breeds based on the results of a comparative analysis of FST and XP-EHH for pairs (Kholmogor + Yaroslavl) – Kalmyk indicates significant differences in the breeding goals in different periods of breed formation. Seven ROH islands have been identified, overlapping in museum and modern samples of Kholmogor and Yaroslavl cattle, localized in the known QTL for milk yield, milk composition, growth, body size andfertility, which indicates the long-term use of the above-mentioned indices as target parameters at breeding these breeds. The genes common to modern and historical cattlepopulations of the studied groups have been identified. The identified genomic regions, which are under selection pressure in the historical populations of the studied breeds andoverlap with the signature of selection in the genome of modern representatives of the same breeds, can be used in the selection of animals for inclusion in genetic resourceconservation programs in order to preserve authentic genomic components.

Keywords: cattle, Kholmogor breed, Yaroslavl breed, Kalmyk breed, museum specimens, whole genome sequencing, selection pressure, candidate genes.

 

REFERENCES

  1. Endris M., Feki E. Review on effect of stress on animal productivity and response of animal to stressors. Journal of Animal and Veterinary Advances, 2021, 20(1): 1-14 CrossRef
  2. Shoshin D.E., Erofeev N.G., Sizova E.A., Pavlova M.Yu. Zhivotnovodstvo i kormoproizvodstvo, 2024, 107(3): 138-162 CrossRef (in Russ.).
  3. Jurkovich V., Hejel P., Kovács L. A review of the effects of stress on dairy cattle behaviour. Animals (Basel), 2024, 14(14): 2038 CrossRef
  4. Selye H. A syndrome produced by diverse nocuous agents. Nature, 1936, 138(32): CrossRef
  5. Gebregeziabhear E., Ameha N. The effect of stress on productivity of animals: A review. Journal of Biology, Agriculture and Healthcare, 2015, 5(3): 165-172.
  6. Thoriya A.V., Bhoi D.B., Patel M.A., Kumar A., Raval J.K. Effect of stress on dairy animal reproduction.  Journal of Livestock Science, 2024, 15: 276-284 CrossRef
  7. Rajput A.S., Rajawat D., Jisna K.S., Panwar A., Patra M.K. Transient impacts of vaccination on livestock production: a holistic review. Indian Journal of Animal Health, 2024, 63(1): 29-40 CrossRef
  8. Brown E.J., Vosloo A. The involvement of the hypothalamo-pituitary-adrenocortical axis in stress physiology and its significance in the assessment of animal welfare in cattle. Onderstepoort Journal of Veterinary Research, 2017, 84(1): a1398 CrossRef
  9. Chu B., Marwaha K., Sanvictores T., Awosika A.O., Ayers D. Physiology, stress reaction. In: StatPearls [Internet]. StatPearls Publishing LLC, Treasure Island (FL), 2025. Available: https://www.ncbi.nlm.nih.gov/books/NBK541120/. No date.
  10. Verma O.P., Kumar R., Kumar A., Chand S. Assisted reproductive techniques in farm animal – from artificial insemination to nanobiotechnology. Veterinary World, 2012, 5(5): 301-310 CrossRef
  11. Zinovieva N.A., Pozyabin S.V., Chinarov R.Yu. Assisted reproductive technologies: the history and role in the development of genetic technologies in cattle (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2020, 55(2): 225-242 CrossRef
  12. Velazquez M.A. Assisted reproductive technologies in cattle: Applications in livestock production, biomedical research and conservation biology. Annual Review of Biomedical Sciences, 2008, 10: 36-62 CrossRef
  13. Pestis V.K., Golubets L.V., Deshko A.S. Izvestiya Natsional’noy akademii nauk Belarusi. Seriya agrarnikh nauk, 2019, 57(2): 192-203 CrossRef (in Russ.).
  14. Babenkov V.Yu., Chimidova N.V., Khakhlinov A.I., Ubushieva A.V., Manzhiev V.I. Zhivotnovodstvo i kormoproizvodstvo, 2023,106(1): 67-76 CrossRef (in Russ.).
  15. Callesen H., Greve T., Christensen F. Ultrasonically guided aspiration of bovine follicular oocytes. Theriogenology, 1987, 27: 217.
  16. Kumar B., Manuja A., Aich P. Stress and its impact on farm animals. Frontiers in Bioscience (Elite edition), 2012, 4(5): 1759-1767 CrossRef
  17. Fernandez-Novo A., Pérez-Garnelo S.S., Villagrá A., Pérez-Villalobos N., Astiz S. The effect of stress on reproduction and reproductive technologies in beef cattle-a review. Animals (Basel), 2020, 10(11): 2096 CrossRef
  18. Costa V.G.G., Vieira A.D., Schneider A., Rovani M.T., Gonçalves P.B.D., Gasperin B.G. Systemic inflammatory and stress markers in cattle and sheep submitted to different reproductive procedures. Ciência Rural, 2018, 48: e20180336 CrossRef
  19. King S.L., Hegadoren K.M. Stress hormones: how do they measure up? Biological Research for Nursing, 2002, 4(2): 92-103 CrossRef
  20. Sheriff M.J., Dantzer B., Delehanty B., Palme R., Boonstra R. Measuring stress in wildlife: Techniques for quantifying glucocorticoids. Oecologia, 2011, 166: 869-887 CrossRef
  21. Mazer K.A., Knickerbocker P.L., Kutina K.L., Huzzey J.M. Changes in behavior and fecal cortisol metabolites when dairy cattle are regrouped in pairs versus individually after calving. Journal of Dairy Science, 2020, 103: 4681-4690 CrossRef
  22. MohanKumar S.M.J., Balasubramanian P., Dharmaraj M., MohanKumar P.S. neuroendocrine regulation of adaptive mechanisms in livestock. In: Environmental stress and amelioration in livestock production. V. Sejian, S. Naqvi, T. Ezeji, J. Lakritz, R. Lal (eds.). Springer, Berlin, 2012: 263-298 CrossRef
  23. Ombelet W., Van Robays J. Artificial insemination history: hurdles and milestones. Facts, Views & Vision in ObGyn, 2015, 7(2): 137-143.
  24. Ferreira V., Ferreira G. Effect of artificial insemination, ruminal incubation, and esophageal tubing on cortisol concentration in blood of lactating dairy cows. JDS Communications, 2025, 6(2): 241-244 CrossRef
  25. Carrell R.S., Smith W.B., Kinman L.A., Mercadante V.R.G., Dias N.W., Roper D.A. Cattle stress and pregnancy responses when imposing different restraint methods for conducting fixed time artificial insemination. Animal Reproduction Science, 2021, 225: 106672 CrossRef
  26. Mujuni P.F., Mgongo F.O.K. Rectal palpation in bovine female reproduction: advantages, risks and procedure. A review. Tanzania Veterinary Journal, 1991, 11(1): 24-42.
  27. Christiansen D. Pregnancy diagnosis: Rectal palpation. In: Bovine reproduction, First edition. R.M. Hopper (ed.). John Wiley & Sons, Inc., 2015: 314-319 CrossRef
  28. Nakao T., Sato T., Moriyoshi M., Kawata K. Plasma cortisol response in dairy cows to vaginoscopy, genital palpation per rectum and artificial insemination. Zentralblatt für Veterinärmedizin. Reihe A, 1994, 41(1): 16-21 CrossRef
  29. Giese H., Dilly M., Gundelach Y., Hoffmann G., Schmicke M. Influence of transrectal palpation training on cortisol levels and heart rate variability in cows. Theriogenology, 2018, 119: 238-244 CrossRef
  30. Kovács L., Tőzsér J., Szenci O., Póti P., Kézér F.L., Ruff F., Gábriel-Tőzsér G., Hoffmann D., Bakony M., Jurkovich V. Cardiac responses to palpation per rectum in lactating and nonlactating dairy cows. Journal of Dairy Science, 2014, 97(11): 6955-6963 CrossRef
  31. Pilz M., Fischer-Tenhagen C., Grau M., Heuwieser W. Behavioural and physiological assessment of stress reactions during vaginal examination in dairy cows. Tierarztliche Praxis Ausgabe G: Grosstiere —Nutztiere, 2014, 42(2): 88-94 CrossRef
  32. Alvi M.A., Khan R., Ullah N., Ihtisham-ul-Haq M. Measurement of stress level in buffaloes by the effect of repeated rectal palpation in teaching environment. Pakistan Journal of Science, 2023, 75(02): 398-418 CrossRef
  33. Grzeczka A., Wozniak G., Graczyk S., Wyszkowska J. Effect of rectal examination on the behavior of multiparous cows (Bos taurus taurus) assessed on the basis of selected stress indicators. Medycyna Weterynaryjna, 2025, 81(3): 108-114 CrossRef
  34. López S.R. Ovum Pick-Up (OPU) in cattle: an update. In: Biotechnologies applied to animal reproduction. First edition. J.C. Gardón, K. Satué (eds.). Apple Academic Press, NY, 2020: 139-183 CrossRef
  35. Chinarov R.Yu., Lukanina V.A., Pozyabin S.V., Singina G.N. The influence of individual features and the breed of donor heifers on the efficiency of oocyte retrieval by ovum pick-up. Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2022, 57(6): 1188-1196 CrossRef
  36. Petyim S., Båge R., Madej A., Larsson B. Ovum pick-up in dairy heifers: Does it affect animal well-being? Reproduction in Domestic Animals, 2007, 42: 623-632 CrossRef
  37. Chastant-Maillard S., Quinton H., Lauffenburger J., Cordonnier-Lefort N., Richard C., Marchal J., Mormede P., Renard J.P. Consequences of transvaginal follicular puncture on well-being in cows. Reproduction, 2003, 125: 555-563 CrossRef
  38. Bomzon A. Pain and stress in cattle: a personal perspective. Israel Journal of Veterinary Medicine, 2011, 66(2): 12-20.
  39. Pisarenko A.V. Heat tolerance of cattle and the influence of heat stress on economically useful traits (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2025, 60(2): 199-219 CrossRef
  40. Mićić N., Bogdanović V., Stanojević D., Gavran M., Samardžija M., Kostelić A., Gantner V. Comprehensive review of heat stress effects on dairy cattle: the implications for production, reproduction, and adaptation in the context of climate change. Veterinarski Arhiv, 2025, 95(4): 365-380 CrossRef
  41. Dash S., Chakravarty A.K., Singh A., Upadhyay A., Singh M., Yousuf S. Effect of heat stress on reproductive performances of dairy cattle and buffaloes: A review. Veterinary World, 2016, 9(3): 235-244 CrossRef
  42. Wang J., Li J., Wang F., Xiao J., Wang Y., Yang H., Li S., Cao Z. Heat stress on calves and heifers: a review. Journal of Animal Science and Biotechnology, 2020, 11: 79 CrossRef
  43. Szalai S., Bodnár Á., Fébel H., Bakony M., Jurkovich V. Effects of heat stress on estrus expression and pregnancy in dairy cows. Animals, 2025, 15: 1688 CrossRef
  44. De Rensis F., Saleri R., Garcia-Ispierto I., Scaramuzzi R., López-Gatius F. Effects of heat stress on follicular physiology in dairy cows. Animals, 2021, 11: 3406 CrossRef
  45. Gendelman M., Aroyo A., Yavin S., Roth Z. Seasonal effects on gene expression, cleavage timing, and developmental competence of bovine preimplantation embryos. Reproduction, 2010, 140: 73-82 CrossRef
  46. Edwards J.L., Saxton A.M., Lawrence J.L., Payton R.R., Dunlap J.R. Exposure to a physiologically relevant elevated temperature hastens in vitro maturation in bovine oocytes. Journal of Dairy Science, 2005, 88(12): 4326-4333 CrossRef
  47. Singh M., Chaudhari B.K., Singh J.K., Singh A.K., Maurya P.K. Effects of thermal load on buffalo reproductive performance during summer season. Journal of Biological Sciences, 2013, 1: 1-8.
  48. Khodaei-Motlagh M.M., Zare Shahneh A., Masoumi R., Derensis F. Alterations in reproductive hormones during heat stress in dairy cattle. African Journal of Biotechnology, 2011, 10: 5552-5558.
  49. Roman-Ponce H., Thatche W.W., Caton D., Barron D.H., Wilcox C.J. Thermal stress effects on uterine blood flow in dairy cows. Journal of Animal Science, 1978, 46(1): 175-180 CrossRef
  50. Mondal S., Mor A., Reddy I.J., Nandi S., Gupta P.S.P. Effect of heat exposure on prostaglandin production and expression of COX-2, PGES, PGFS, ITGAV and LGALS15 mRNAs in endometrial epithelial cells of buffalo (Bubalus bubalis). Molecular Biology Reports, 2024, 51(1): 405 CrossRef
  51. Succu S., Sale S., Ghirello G., Ireland J., Evans A., Atzori A., Mossa F. Exposure of dairy cows to high environmental temperatures and their lactation status impairs establishment of the ovarian reserve in their offspring. Journal of Dairy Science, 2020, 103(12): 11957-11969 CrossRef
  52. Badinga L., Collier R.J., Thatcher W.W., Wilcox C.J. Effects of climatic and management factors on conception rate of dairy cattle in subtropical environment. Journal of Dairy Science, 1985, 68(1): 78-85 CrossRef
  53. Macedo G.G., Zúccari C.E.S.N., de Abreu U.G.P., Negrão J.A., da Costa e Silva E.V. Human–animal interaction, stress, and embryo production in Bos indicus embryo donors under tropical conditions. Tropical Animal Health and Production, 2011, 43: 1175-1182 CrossRef
  54. Creamer M., Horback K. Researching human-cattle interaction on rangelands: challenges and potential solutions. Animals, 2021, 11: 725 CrossRef
  55. Acharya R.Y., Hemsworth P.H., Coleman G.J., Kinder J.E. The animal-human interface in farm animal production: animal fear, stress, reproduction and welfare. Animals (Basel), 2022, 12(4): 487 CrossRef
  56. Zhuchaev K.V., Kochneva M.L., Borisenko E.A. Welfare of productive animals (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2024, 59(6): 1025-1038 CrossRef
  57. Waiblinger S., Menke C., Korff J. & Bucher A. Previous handling and gentle interactions affect behaviour and heart rate of dairy cows during a veterinary procedure. Applied Animal Behaviour Science, 2004, 85(1): 31-42 CrossRef
  58. Schmied C., Boivin X., Waiblinger S. Stroking different body regions of dairy cows: Effects on avoidance and approach behavior toward humans. Journal of Dairy Science, 2008, 91: 596-605 CrossRef
  59. Lürzel S., Barth K., Windschnurer I., Futschik A., Waiblinger S. The influence of gentle interactions during milking on dairy cows’ avoidance distance and milk yield, flow and composition. Animal, 2018, 12: 340-349 CrossRef
  60. Durocher J., Morin N., Blondin P. Effect of hormonal stimulation on bovine follicular response and oocyte developmental competence in a commercial operation. Theriogenology, 2006, 65(1): 102-115 CrossRef
  61. Gou K.-M., Guan H., Bai J.-H., Cui X.-H., Wu Z.-F., Yan F.-X., An X.-R. Field evaluation of juvenile in vitro embryo transfer (JIVET) in sheep. Animal Reproduction Science, 2009, 112(3-4): 316-324 CrossRef
  62. Hafez Y.M. Assisted reproductive technologies in farm animals. Proc. of the 2nd International Conference on the Modern Approaches in Livestock's Production Systems (ICMALPS). Alexandria University, Egypt, 2015: 91-1184.
  63. Rhinehart J., Pohler K., Anderson L. Physiological factors affecting success to reproductive technologies. In: Applied reproductive strategies in beef cattle. Iowa, 2016: 6-16.
  64. Singina G.N., Chinarov R.Yu., Shedova E.N. Dostizheniya nauki i tekhniki APK, 2023, 37(11): 59-64 CrossRef (in Russ.).
  65. Dehdehi L., Novin M.G., Sadeghi Y. Chronic stress diminishes the oocyte quality and in vitro embryonic development in maternally separated mice. International Journal of Women s Health and Reproduction Sciences, 2020, 8(1): 29-36 CrossRef
  66. Lebedeva D.A., Igonina T.N., Brusentsev E.Yu., Shavshaeva N.A., Amstislavskiy S.Ya. Rossiyskiy fiziologicheskiy zhurnal im. I.M. Sechenova, 2024, 110(6): 930-944 CrossRef (in Russ.).
  67. Sun J., Guo Y., Zhang Q., Bu S., Li B., Wang Q., Lai D. Chronic restraint stress disturbs meiotic resumption through APC/C-mediated cyclin B1 excessive degradation in mouse oocytes. Cell Cycle, 2018, 17(13): 1591-1601 CrossRef
  68. Casillas F., Flores-González A., Juárez-Rojas L., López A., Betancourt M., Casas E., Bahena I., Bonillac E. Chronic stress decreases fertility parameters in female rats. Systems Biology in Reproductive Medicine, 2023, 69(3): 234-244 CrossRef
  69. Chen R.R., Wang J., Zhang M., Kong Q.Q., Sun G.Y., Jin C.H., Luo M.J., Tan J.H. Restraint stress of female mice during oocyte development facilitates oocyte postovulatory aging. Aging (Albany NY), 2022, 14(22): 9186-9199 CrossRef
  70. Zhao L.H., Cui X.Z., Yuan H.J., Liang B., Zheng L.L., Liu Y.X., Luo M.J., Tan J.H. Restraint stress inhibits mouse implantation: temporal window and the involvement of HB-EGF, estrogen and progesterone. PLoS ONE, 2013, 8(11): e80472 CrossRef
  71. Shiryaev G.V., Prituzhalova A.O., Nikitin G.S., Nikitkina E.V., Musidray A.A., Alekseeva A.Yu. The influence of various kisspeptins on the reproductive function of Bos taurus (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2023, 58(6): 974-989 CrossRef
  72. Domes G., Linnig K., von Dawans B. Gonads under stress: a systematic review and meta-analysis on the effects of acute psychosocial stress on gonadal steroids secretion in humans. Psychoneuroendocrinology, 2024, 164: 107004 CrossRef
  73. Dobson H., Smith R.F. Stress and reproduction in farm animals. Journal of Reproduction and Fertility. Supplement, 1995, 49: 451-461.
  74. Cook D.L., Winters T.A., Horstman L.A., Allrich R.D. Influence of cortisol and dexamethasone on estrous behavior of estradiol-treated ovariectomized cows and heifers. Journal of Dairy Science, 1987, 70: 181-185 CrossRef
  75. Walker S.L., Smith R.F., Jones D.N., Routly J.E., Dobson H. Chronic stress, hormone profiles and estrus intensity in dairy cattle. Hormones and Behavior, 2008, 53(3): 493-501 CrossRef
  76. Wei Y., Li W., Meng X., Zhang L., Shen M., Liu H. Corticosterone injection impairs follicular development, ovulation and steroidogenesis capacity in mice ovary. Animals, 2019, 9: 1047 CrossRef
  77. Kala M., Nivsarkar M. Role of cortisol and superoxide dismutase in psychological stress induced anovulation. General and Comparative Endocrinology, 2016, 225: 117-124 CrossRef
  78. Mahdy A.K.H., da Silva M.H.M., da Silva F.M. Effect of cortisol on bovine oocytes maturation and further embryonic development after in vitro fertilization. Biomedical Journal of Scientific & Technical Research, 2018, 10(4): 8029-8034 CrossRef
  79. Burkuš J., Kačmarová M., Kubandová J., Kokošová N., Fabianová K., Fabian D., Koppel J., Čikoš Š. Stress exposure during the preimplantation period affects blastocyst lineages and offspring development. The Journal of Reproduction and Development, 2015, 61(4): 325-331 CrossRef
  80. Wahl F., Huo J., Du S., Schoen J., Chen S. Maternal stress and the early embryonic microenvironment: investigating long-term cortisol effects on bovine oviductal epithelial cells using air–liquid interface culture. Journal of Animal Science and Biotechnology,2024, 15: 129 CrossRef
  81. Faria N., Pacheco-Lima J., Moreira da Silva M.H., Borba A., Moreira da Silva J.F. Effects of cortisol levels on reproductive success in cattle of different temperaments during fixed-time artificial insemination (FTAI). Journal of Animal Behaviour and Biometeorology, 2024, 12(1): 2024002 CrossRef
  82. Arck P. Stress et implantation [Stress and embryo implantation]. Journal de Gynecologie, Obstetricue et Biologie de la Reproduction (Paris), 2004, 33(1/Pt 2): S40-42 CrossRef
  83. Kasimanickam R., Schroeder S., Assay M., Kasimanickam V., Moore D., Gay J., Whittier W. Influence of temperament score and handling facility on stress, reproductive hormone concentrations, and fixed time AI pregnancy rates in beef heifers. Reproduction in Domestic Animals, 2014, 49: 775-782 CrossRef
  84. Kasimanickam V., Abdel Aziz R., Williams H., Kasimanickam R. Predictors of beef calf temperament at weaning and its impact on temperament at breeding and reproductive performance. Reproduction in Domestic Animals, 2018, 53(2): 484-494 CrossRef
  85. Kovács L., Kézér F.L., Kulcsár-Huszenicza M., Ruff F., Szenci O., Jurkovich V. Hypothalamic-pituitary-adrenal and cardiac autonomic responses to transrectal examination differ with behavioral reactivity in dairy cows. Journal of Dairy Science, 2016, 99(9): 7444-7457 CrossRef
  86. Cooke R.F., Arthington J.D., Araujo D.B., Lamb G.C. Effects of acclimation to human interaction on performance, temperament, physiological responses, and pregnancy rates of Brahman-crossbred cows. Journal of Animal Science, 2009, 87(12): 4125-4132 CrossRef
  87. Heck A.L., Handa R.J. Sex differences in the hypothalamic-pituitary-adrenal axis' response to stress: an important role for gonadal hormones. Neuropsychopharmacology, 2019, 44(1): 45-58 CrossRef
  88. Zuloaga D.G., Heck A.L., De Guzman R.M., Handa R.J. Roles for androgens in mediating the sex differences of neuroendocrine and behavioral stress responses. Biology of Sex Differences, 2020, 11(1): 44 CrossRef
  89. Viau V., Meaney M.J. Variations in the hypothalamic-pituitary-adrenal response to stress during the estrous cycle in the rat. Endocrinology, 1991, 129(5): 2503-2511 CrossRef
  90. Nickolov V., Ivanova E. Influence of stress with different power and time of action on reproduction performance in bulls. Bulgarian Journal of Agricultural Science, 1995, 1: 329-335.
  91. Pérez-Garnelo S.S., Utrilla M.J., Fernández-Novo A., Revilla-Ruiz Á., Villagrá A., Astiz S. Effect of stress on reproduction and reproductive technologies in male and female, beef and dairy cattle. In: Assisted reproductive technologies in animals V. 1. J.C. Gardón, K. Satué Ambrojo (eds.). Springer, Cham, 2024: 127-193 CrossRef
  92. Möstl E., Choi H.S., Bamberg E. Stimulation of androgen and oestrogen concentrations in plasma of cows after administration of a synthetic glucocorticoid (flumethasone) at the end of gestation. The Journal of Endocrinology, 1985, 105(1): 121-126 CrossRef
  93. Spicer L.J., Zinn S.A. Relationship between concentrations of cortisol in ovarian follicular fluid and various biochemical markers of follicular differentiation in cyclic and an ovulatory cattle.  Journal of Reproduction and Fertility, 1987, 81: 221-226 CrossRef
  94. Dong J., Li J., Li J., Cui L., Meng X., Qu Y., Wang H. The proliferative effect of cortisol on bovine endometrial epithelial cells. Reproductive Biology and Endocrinology, 2019, 17(1): 97 CrossRef
  95. Abilov A.I., Gudilina A.A., Kombarova N.A., Turbina V.V., Korneenko-Zhilyaev Yu.A. Cortisol as a marker of physiological stress in Bos taurus sires. Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2024, 59(2): 301-315 CrossRef

back

 


CONTENTS

 

Full article PDF (Rus)