Neurologic dysfunction in newborn calves: understanding neonatal encephalopathy in clinical practice

  • Bailey Bailey College of Veterinary Medicine, Washington State University, Pullman, WA, USA
  • Ramanathan Kasimanickam College of Veterinary Medicine, Washington State University, Pullman, WA, USA https://orcid.org/0000-0003-1117-7867
Keywords: Cattle, calf, neonatal encephalopathy, maladjustment syndrome, perinatal hypoxia, progesterone, gut microbiome

Abstract

Neonatal encephalopathy (NE), a clinically important syndrome causing neurologic dysfunction in newborn calves, contributes to early-life morbidity and mortality. Affected calves exhibit impaired adaptation to extrauterine life, including delayed or absent respiration, difficulty standing, and ineffective nursing, compromising colostrum intake, passive immunity transfer, and overall viability. NE reflects a clinical presentation rather than a specific etiologic diagnosis and may result from hypoxic-ischemic injury, metabolic disturbances, trauma, infection, or intoxication. Historical terms such as ‘dummy calf’ and weak calf syndrome lack diagnostic precision and should be interpreted cautiously. Neonatal maladjustment syndrome, derived largely from equine and human literature, represents a proposed mechanistic subset of NE, potentially involving persistent neurosteroid activity but remains speculative in calves. Emerging hypotheses, including neurosteroid persistence and maternal gut microbiome influences, may contribute to neonatal maladaptation but require further validation. Management is primarily supportive whereas prevention should focus on dystocia reduction, timely obstetric intervention, and optimized periparturient and early neonatal care. Clarifying terminology and understanding underlying mechanisms is essential to improve clinical decision-making and research interpretation.

Downloads

Download data is not yet available.

References


1.
Probo M, Veronesi MC: Clinical scoring systems in the newborn calf: an overview. Animals (Basel) 2022;12:3013. doi: 10.3390/ani12213013

2.
Mee JF: Newborn dairy calf management. Vet Clin North Am Food Anim Pract 2008;24:1–17. doi: 10.1016/j.cvfa.2007.10.002

3.
Mee JF: Neonatal calf vitality. In: Simões J: editor. Encyclopedia of Livestock Medicine for Large Animal and Poultry Production. Springer; Cham: 2025. p. 1–44.

4.
Bienboire-Frosini C, Muns R, Marcet-Rius M, et al: Vitality in newborn farm animals: adverse factors, physiological responses, pharmacological therapies, and physical methods to increase neonate vigor. Animals (Basel) 2023;13:1542. doi: 10.3390/ani13091542

5.
Murray CF, Leslie KE: Newborn calf vitality: risk factors, characteristics, assessment, resulting outcomes and strategies for improvement. Vet J 2013;198:322–328. doi: 10.1016/j.tvjl.2013.06.007

6.
Gamsjäger L, Haines DM, Pajor EA, et al: Impact of volume, immunoglobulin G concentration, and feeding method of colostrum product on neonatal nursing behavior and transfer of passive immunity in beef calves. Animal 2021;15:100345. doi: 10.1016/j.animal.2021.100345

7.
Homerosky ER, Caulkett NA, Timsit, et al: Clinical indicators of blood gas disturbances, elevated L-lactate concentration and other abnormal blood parameters in newborn beef calves. Vet J 2017;219:49–57. doi: 10.1016/j.tvjl.2016.12.001

8.
Stauber EH: Weak calf syndrome: a continuing enigma. J Am Vet Med Assoc 1976;168:223–225. doi: 10.2460/javma.1976.168.03.223

9.
Constable PD, Hinchcliff KW, Done SH, et al: Perinatal diseases. In: Veterinary Medicine: A Textbook of the Diseases of Cattle, Horses, Sheep, Pigs and Goats. 11th edition, St. Louis, MO; Elsevier: 2017. p. 1830–1903.

10.
Bianco AW, Moore GE, Taylor SD: Neonatal encephalopathy in calves presented to a university hospital. J Vet Intern Med 2017;31:1892–1899. doi: 10.1111/jvim.14821

11.
Barrier AC, Haskell MJ, Birch S, et al: The impact of dystocia on dairy calf health, welfare, performance and survival. Vet J 2013;195:86–90. doi: 10.1016/j.tvjl.2012.07.031

12.
Ward J: Weak calf syndrome. Proc Am Assoc Bovine Pract 1973; p. 97–105.

13.
Mee JF: Why do so many calves die on modern dairy farms and what can we do about calf welfare in the future? Animals (Basel) 2013;3:1036–1057. doi: 10.3390/ani3041036

14.
Norquay R, Orr J, Norquay B, et al: Perinatal mortality in 23 beef herds in Orkney: incidence, risk factors and aetiology. Vet Rec 2020;187:28. doi: 10.1136/vr.105536

15.
Abutarbush SM, Radostits OM: Congenital nutritional muscular dystrophy in a beef calf. Can Vet J 2003;44:738–739.

16.
Baker JC: The clinical manifestations of bovine viral diarrhea infection. Vet Clin North Am Food Anim Pract 1995;11:425–445. doi: 10.1016/s0749-0720(15)30460-6

17.
Jung Y, Kim B, Ku JY, et al: Physiological alterations and predictors of death in neonatal calves with weak calf syndrome. Vet Rec 2025;197(3):e5327. doi: 10.1002/vetr.5327

18.
Rowan TG: Thermoregulation in neonatal ruminants. In: Varley MA, Williams PEV, Lawrence TLJ: editors. Neonatal Survival and Growth. Edinburgh, UK; British Society of Animal Production: 1992. p. 13–24.

19.
Mota-Rojas D, Wang D, Titto CG, et al: Neonatal infrared thermography images in the hypothermic ruminant model: anatomical-morphological-physiological aspects and mechanisms for thermoregulation. Front Vet Sci 2022;9:963205. doi: 10.3389/fvets.2022.963205

20.
Mohseni S: Neurologic damage in hypoglycemia. Handb Clin Neurol 2014;126:513–532. doi: 10.1016/B978-0-444-53480-4.00036-9

21.
Tennant B, Harrold D, Reina-Guerra M: Hypoglycemia in neonatal calves associated with acute diarrhea. Cornell Vet 1968;58:136–146.

22.
Ider M, Naseri A, Ok M, et al: Surveilling brain damage using brain biomarkers in hypoglycemic neonatal calves with diarrhea. Front Vet Sci 2023;10:1240846. doi: 10.3389/fvets.2023.1240846

23.
Dore V, Smith G: Cerebral disorders of calves. Vet Clin North Am Food Anim Pract 2017;33:27–41. doi: 10.1016/j.cvfa.2016.09.004

24.
Mee JF, Sánchez-Miguel C, Doherty M: Influence of modifiable risk factors on the incidence of stillbirth/perinatal mortality in dairy cattle. Vet J 2014;199:19–23. doi: 10.1016/j.tvjl.2013.08.004

25.
Smyth JA, Fitzpatrick DA, Ellis WA: Stillbirth/perinatal weak calf syndrome: a study of calves infected with Leptospira. Vet Rec 1999;145:539–42. doi: 10.1136/vr.145.19.539

26.
Gardiner RM: Cerebral blood flow and oxidative metabolism during hypoxia and asphyxia in the new-born calf and lamb. J Physiol 1980;305:357–76. doi: 10.1113/jphysiol.1980.sp013369

27.
Hammer CJ, Tyler HD: Effects of early rupture of the umbilical vessels in Jersey calves. J Dairy Sci 1999;82 Suppl:49.

28.
Szenci O, Taverne MA, Bakonyi S, et al: Comparison between pre- and postnatal acid-base status of calves and their perinatal mortality. Vet Q 1988;10:140–144. doi: 10.1080/01652176.1988.9694161

29.
Mee JF: Premature expulsion of the placenta and bovine perinatal mortality. Vet Rec 1991;128:521–523. doi: 10.1136/vr.128.22.521

30.
Smail NL, Adnane M, Wagener K, et al: Roadmap to dystocia management-guiding obstetric interventions in cattle. Life (Basel) 2025;15:457. doi: 10.3390/life15030457

31.
Wood CE, Keller-Wood M: Current paradigms and new perspectives on fetal hypoxia: implications for fetal brain development in late gestation. Am J Physiol Regul Integr Comp Physiol 2019;317:R1–R13. doi: 10.1152/ajpregu.00008.2019

32.
Mota-Rojas D, Villanueva-García D, Solimano A, et al: Pathophysiology of perinatal asphyxia in humans and animal models. Biomedicines 2022;10:347. doi: 10.3390/biomedicines10020347

33.
Garfinkle J, Steven P, Miller SP: The placenta and neurodevelopment in preterm newborns. Neoreviews 2018;19:e456–e466. doi: 10.1542/neo.19-8-e456

34.
Almeida A, Delgado-Esteban M, Bolaños JP, et al: Oxygen and glucose deprivation induces mitochondrial dysfunction and oxidative stress in neurones but not in astrocytes in primary culture. J Neurochem 2002;81:207–217. doi: 10.1046/j.1471-4159.2002.00827.x

35.
Jagečić D, Petrović DJ, Šimunić I, et al: The oxygen and glucose deprivation of immature cells of the nervous system exerts distinct effects on mitochondria, mitophagy, and autophagy, depending on the cells’ differentiation stage. Brain Sci 2023;13:910. doi: 10.3390/brainsci13060910

36.
Woods JR Jr: Birth asphyxia: pathophysiologic events and fetal adaptive changes. Clin Perinatol 1983;10:473–486. doi: 10.1016/S0095-5108(18)30980-1

37.
Fellman V, Raivio KO: Reperfusion injury as the mechanism of brain damage after perinatal asphyxia. Pediatr Res 1997;41:599–606. doi: 10.1203/00006450-199705000-00001

38.
Hirst JJ, Palliser HK, Yates DM, et al: Neurosteroids in the fetus and neonate: potential protective role in compromised pregnancies. Neurochem Int 2008;52:602–610. doi: 10.1016/j.neuint.2007.07.018

39.
Slotkin TA, Lagercrantz H: The stress of being born. Sci Am 1986;254:100. doi: 10.1038/scientificamerican0486-100

40.
Baulieu EE: Neurosteroids: of the nervous system, by the nervous system, for the nervous system. Recent Prog Horm Res 1997;52:1–32.

41.
Zhu W, Huang L, Cheng H, et al: GABA and its receptors’ mechanisms in the treatment of insomnia. Heliyon 2024;10:e40665. doi: 10.1016/j.heliyon.2024.e40665

42.
Chen RJ, Sharma S: GABA receptor. In: StatPearls [Internet]. Treasure Island, FL; StatPearls Publishing: 2025. [updated 18 February 2025]. Available from: https://www.ncbi.nlm.nih.gov/books/NBK526124/ [cited 25 June 2025].

43.
Pinna G, Uzunova V, Matsumoto K, et al: Brain allopregnanolone regulates the potency of the GABAA receptor agonist muscimol. Neuropharmacology 2000:39:440–448. doi: 10.1016/S0028-3908(99)00149-5

44.
Timby E, Balgård M, Nyberg S, et al: Pharmacokinetic and behavioral effects of allopregnanolone in healthy women. Psychopharmacology (Berl) 2006;186:414–424. doi: 10.1007/s00213-005-0148-7

45.
van Broekhoven F, Bäckström T, van Luijtelaar G, et al: Effects of allopregnanolone on sedation in men, and in women on oral contraceptives. Psychoneuroendocrinology 2007;32:555–564. doi: 10.1016/j.psyneuen.2007.03.009

46.
Hu Y, Jin P, Peng J, et al: Different immunological responses to early-life antibiotic exposure affecting autoimmune diabetes development in NOD mice. J Autoimmun 2016;72:47–56. doi: 10.1016/j.jaut.2016.05.001

47.
Braniste V, Al-Asmakh M, Kowal C, et al: The gut microbiota influences blood-brain barrier permeability in mice. Sci Transl Med. 2014;6:263ra158. doi: 10.1126/scitranslmed.3009759

48.
Stilwell G, Mellor DJ, Holdsworth SE: Potential benefit of a thoracic squeeze technique in two newborn calves delivered by caesarean section. N Z Vet J 2020;68:65–68. doi: 10.1080/00480169.2019.1670115

49.
Jöchle W, Esparza H, Giménez T, et al: Inhibition of corticoid-induced parturition by progesterone in cattle: effect on delivery and calf viability. J Reprod Fertil 1972;28:407–412. doi: 10.1530/jrf.0.0280407

50.
Kindahl H, Kornmatitsuk B, Königsson K, et al: Endocrine changes in late bovine pregnancy with special emphasis on fetal well-being. Domest Anim Endocrinol 2002;23:321–328. doi: 10.1016/s0739-7240(02)00167-4

51.
Hirst JJ, Yawno T, Nguyen P, et al: Stress in pregnancy activates neurosteroid production in the fetal brain. Neuroendocrinology 2006;84:264–274. doi: 10.1159/000097990

52.
Brunton PJ, Russell JA, Hirst JJ: Allopregnanolone in the brain: protecting pregnancy and birth outcomes. Prog Neurobiol 2014;113:106–136. doi: 10.1016/j.pneurobio.2013.08.005

53.
Bleul U: Respiratory distress syndrome in calves. Vet Clin North Am Food Anim Pract 2009;25:179–193. doi: 10.1016/j.cvfa.2008.10.002

54.
Bellows RA, Lammoglia MA: Effects of severity of dystocia on cold tolerance and serum concentrations of glucose and cortisol in neonatal beef calves. Theriogenology 2000;53:803–813. doi: 10.1016/S0093-691X(99)00275-7

55.
Frosali S, Di Simplicio P, Perrone S, et al: Glutathione recycling and antioxidant enzyme activities in erythrocytes of term and preterm newborns at birth. Biol Neonate 2004;85:188–194. doi: 10.1159/000075814

56.
Rice LE: Dystocia-related risk factors. Vet Clin North Am Food Anim Pract 1994;10:53–68. doi: 10.1016/s0749-0720(15)30589-2

57.
Kirovski D: Endocrine and metabolic adaptations of calves to extra-uterine life. Acta Vet Beograd 2015;65:297–318. doi: 10.1515/acve-2015-0025

58.
Smith GW: Resuscitation of the newborn calf. Proc Am Assoc Bovine Pract 2022;55:108–110. doi: 10.21423/aabppro20228617

59.
Bleul U, Wey C, Meira C, et al: Assessment of postnatal pulmonary adaption in bovine neonates using electric impedance tomography (EIT). Animals (Basel) 2021;11:3216. doi: 10.3390/ani11113216

60.
Rollin F, Danlois F, Alianoui H, et al: Respiratory distress syndrome in full-term newborn calves. Academia.edu: 2017. Available from: https://calfsessions.com/wp-content/uploads/2017/10/Calf-Sessions-template_Respiratory-Distress-Syndrome.pdf [cited 4 August 2025].

61.
Donnelly CG, Quinn CT, Nielsen SG, et al: Respiratory support for pharmacologically induced hypoxia in neonatal calves. Vet Med Int 2016;2016:2129362. doi: 10.1155/2016/2129362

62.
Wichman LG, Redifer CA, Meyer AM: Maternal nutrient restriction during late gestation reduces vigor and alters blood chemistry and hematology in neonatal beef calves. J Anim Sci 2023;101:skad342. doi: 10.1093/jas/skad342

63.
Caton JS, Hess BW: Maternal plane of nutrition: impacts on fetal outcomes and postnatal offspring responses. In: Proc Graz Lives Nutr Conf, Casper, WY, 2010, pp. 104–119.

64.
Funston RN, Larson DM, Vonnahme KA: Effects of maternal nutrition on conceptus growth and offspring performance: implications for beef cattle production. J Anim Sci 2010;88(13 Suppl):E205–E215. doi: 10.2527/jas.2009-2351

65.
Quigley JD 3rd, Drewry JJ: Nutrient and immunity transfer from cow to calf pre- and postcalving. J Dairy Sci 1998;81:2779–2790. doi: 10.3168/jds.S0022-0302(98)75836-9

66.
Carstens GE: Cold thermoregulation in the newborn calf. Vet Clin North Am Food Anim Pract 1994;10:69–106. doi: 10.1016/S0749-0720(15)30590-9

67.
Okamoto M, Robinson JB, Christopherson RJ, et al: Summit metabolism of newborn calves with and without colostrum feeding. Can J Anim Sci 1986;66:937–944. doi: 10.4141/cjas86-103

68.
Azzam SM, Kinder JE, Nielsen MK, et al: Environmental effects on neonatal mortality of beef calves. J Anim Sci 1993;71:282–290. doi: 10.2527/1993.712282x

69.
Takahashi K, Takahashi E, Ducusin RJ, et al: Changes in serum thyroid hormone levels in newborn calves as a diagnostic index of endemic goiter. J Vet Med Sci 2001;63:175–178. doi: 10.1292/jvms.63.175

70.
USDA. Death loss in U.S. cattle and calves due to predator and nonpredator causes, 2015. Fort Collins (CO); USDA–APHIS–VS–CEAH: 2017. Available from: https://www.aphis.usda.gov/sites/default/files/cattle_calves_deathloss_2015.pdf [cited 25 June 2025]

71.
Lombard JE, Garry FB, Tomlinson SM, et al: Impacts of dystocia on health and survival of dairy calves. J Dairy Sci 2007;90:1751–1760. doi: 10.3168/jds.2006-295

72.
Aleman M, Chigerwe M, Varga A, et al: Steroid precursors, steroids, neuroactive steroids, and neurosteroids concentrations in serum and saliva of healthy neonatal heifer Holstein calves. J Vet Intern Med 2020;34:2767–2775. doi: 10.1111/jvim.15957

73.
Bernard WV, Reimer JM, Cudd T: Historical factors, clinicopathologic findings, clinical features, and outcome of equine neonates presenting with or developing signs of central nervous system disease. Proc Am Assoc Equine Pract 1995;41:222–224.

74.
Mee JF: Impacts of dairy cow nutrition precalving on calf health. JDS Commun 2023;4:245–249. doi: 10.3168/jdsc.2022-0281

75.
Nonnecke BJ, Foote MR, Miller BL, et al: Effects of chronic environmental cold on growth, health, and select metabolic and immunologic responses of preruminant calves. J Dairy Sci 2009;92:6134–6143. doi: 10.3168/jds.2009-2517

76.
Young BA: Ruminant cold stress: effect on production. J Anim Sci 1983;57(6):1601–1607. doi: 10.2527/jas1983.5761601x

77.
Majors C, Myers A, Kasimanickam R: Selenium in cattle diseases and reproductive health. Clinical Theriogenology 2025;17:1–18. doi: 10.58292/CT.v17.12015

78.
Waldner CL, Uehlinger FU: Factors associated with serum vitamin A and vitamin E concentrations in beef calves from Alberta and Saskatchewan and the relationship between vitamin concentrations and calf health outcomes. Can J Anim Sci 2017;97:65–82. doi: 10.1139/cjas-2016-0055

79.
Grooms DL: Reproductive consequences of infection with bovine viral diarrhea virus. Vet Clin North Am Food Anim Pract 2004;20:5–19. doi: 10.1016/j.cvfa.2003.11.006

80.
Anderson ML: Disorders of cattle. In: Njaan BL: editor. Kirkbride’s Diagnosis of Abortion and Neonatal Loss in Animals. Chichester, West Sussex, UK; Wiley-Blackwell: 2012. p. 30–32.

81.
Kolatorova L, Vitku J, Suchopar J, et al: Progesterone: a steroid with wide range of effects in physiology as well as human medicine. Int J Mol Sci 2022;23:7989. doi: 10.3390/ijms23147989

82.
Hauser CA, Chesnoy-Marchais D, Robel P, et al: Modulation of recombinant alpha 6 beta 2 gamma 2 GABAA receptors by neuroactive steroids. Eur J Pharmacol 1995;289:249–257. doi: 10.1016/0922-4106(95)90101-9

83.
Espinoza TR, Wright DW: The role of progesterone in traumatic brain injury. J Head Trauma Rehabil 2011;26:497–499. doi: 10.1097/HTR.0b013e31823088fa

84.
Zheng C, Gong J, Zang L, et al: Mechanism of progesterone in treatment of traumatic brain injury based on network pharmacology and molecular docking technology. Med Sci Monit 2022;28:e937564. doi: 10.12659/MSM.937564

85.
Schumacher M, Sitruk-Ware R, De Nicola AF: Progesterone and progestins: neuroprotection and myelin repair. Curr Opin Pharmacol 2008;8:740–746. doi: 10.1016/j.coph.2008.10.002

86.
Singh M, Su C: Progesterone, brain-derived neurotrophic factor and neuroprotection. Neuroscience 2013;239:84–91. doi: 10.1016/j.neuroscience.2012.09.056

87.
Singh M, Krishnamoorthy VR, Kim S, et al: Brain-derived neuerotrophic factor and related mechanisms that mediate and influence progesterone-induced neuroprotection. Front Endocrinol 2024;15:1286066. doi: 10.3389/fendo.2024.1286066

88.
Henderson VW: Progesterone and human cognition. Climacteric 2018;21:333–340. doi: 10.1080/13697137.2018.1476484

89.
Sundström Poromaa I, Gingnell M: Menstrual cycle influence on cognitive function and emotion processing-from a reproductive perspective. Front Neurosci 2014;8:380. doi: 10.3389/fnins.2014.00380

90.
Wang J, Chen A: High progesterone levels facilitate women’s social information processing by optimizing attention allocation. Psychoneuroendocrinology 2020;122:104882. doi: 10.1016/j.psyneuen.2020.104882

91.
Conde DM, Verdade RC, Valadares ALR, et al: Menopause and cognitive impairment: a narrative review of current knowledge. World J Psychiatry 2021;11:412–428. doi: 10.5498/wjp.v11.i8.412

92.
Borozan S, Kamrul-Hasan ABM, Pappachan JM: Hormone replacement therapy for menopausal mood swings and sleep quality: the current evidence. World J Psychiatry 2024;14:1605–1610. doi: 10.5498/wjp.v14.i10.1605

93.
Stefaniak M, Dmoch-Gajzlerska E, Jankowska K, et al: Progesterone and its metabolites play a beneficial role in affect regulation in the female brain. Pharmaceuticals (Basel) 2023;16:520. doi: 10.3390/ph16040520

94.
Paul SM, Pinna G, Guidotti A: Allopregnanolone: from molecular pathophysiology to therapeutics. A historical perspective. Neurobiol Stress 2020;12:100215. doi: 10.1016/j.ynstr.2020.100215

95.
Voskuhl R: It is time to conduct phase 3 clinical trials of sex hormones in MS - yes. Mult Scler 2018;24:1413–1415. doi: 10.1177/1352458518768764

96.
Harden CL, Pennell PB: Neuroendocrine considerations in the treatment of men and women with epilepsy. Lancet Neurol 2013;12:72–83. doi: 10.1016/s1474-4422(12)70239-9

97.
Honjo H, Iwasa K, Kawata M, et al: Progestins and estrogens and Alzheimer’s disease. J Steroid Biochem Mol Biol 2005;93:305–308. doi: 10.1016/j.jsbmb.2004.12.001

98.
Partridge B, Rossmeisl JH Jr: Companion animal models of neurological disease. J Neurosci Methods 2020;331:108484. doi: 10.1016/j.jneumeth.2019.108484

99.
De Nicola AF, Coronel F, Garay LI, et al: Therapeutic effects of progesterone in animal models of neurological disorders. CNS Neurol Disord Drug Targets 2013;12:1205–1218. doi: 10.2174/187152731131200120

100.
Grone BP, Baraban SC: Animal models in epilepsy research: legacies and new directions. Nat Neurosci 2015;18:339–343. doi: 10.1038/nn.3934

101.
Van Meervenne SA, Volk HA, Matiasek K, et al: The influence of sex hormones on seizures in dogs and humans. Vet J 2014;201:15–20. doi: 10.1016/j.tvjl.2014.05.008

102.
Van Meervenne SA, Volk HA, Van Ham LM: Association between estrus and onset of seizures in dogs with idiopathic epilepsy. J Vet Intern Med 2015;29(1):251–253. doi: 10.1111/jvim.12505

103.
Freitas-de-Melo A, Banchero G, Hötzel MJ, et al: Progesterone administration reduces the behavioural and physiological responses of ewes to abrupt weaning of lambs. Animal 2013;7:1367–1373. doi: 10.1017/S1751731113000621

104.
Lonergan P, Sánchez JM: Symposium review: progesterone effects on early embryo development in cattle. J Dairy Sci 2020;103:8698–8707. doi: 10.3168/jds.2020-18583

105.
Spencer TE, Burghardt RC, Johnson GA, et al: Conceptus signals for establishment and maintenance of pregnancy. Anim Reprod Sci 2004;82–83:537–550. doi: 10.1016/j.anireprosci.2004.04.014

106.
Pokharel K, Peippo J, Weldenegodguad M, et al: Gene expression profiling of corpus luteum reveals important insights about early pregnancy in domestic sheep. Genes 2020;11:415. doi: 10.3390/genes11040415

107.
Hansen PJ: Regulation of immune cells in the uterus during pregnancy in ruminants. J Anim Sci 2007;85(13 Suppl):E30–E31. doi: 10.2527/jas.2006-487

108.
Dicks LMT: Gut bacteria and neurotransmitters. Microorganisms 2022;10:1838. doi: 10.3390/microorganisms10091838

109.
Ziętek M, Celewicz Z, Szczuko M: Short-chain fatty acids, maternal microbiota and metabolism in pregnancy. Nutrients 2021;13:1244. doi: 10.3390/nu13041244

110.
Vuong HE, Pronovost GN, Williams DW, et al: The maternal microbiome modulates fetal neurodevelopment in mice. Nature 2020;586:281–286. doi: 10.1038/s41586-020-2745-3

111.
Clarke G, Grenham S, Scully P, et al: The microbiome-gut-brain axis during early life regulates the hippocampal serotonergic system in a sex-dependent manner. Mol Psychiatry 2013;18:666–673. doi: 10.1038/mp.2012.77

112.
Bonnin A, Levitt P: Fetal, maternal, and placental sources of serotonin and new implications for developmental programming of the brain. Neuroscience 2011;197:1–7. doi: 10.1016/j.neuroscience.2011.10.005

113.
Sachis PN, Armstrong DL, Becker LE, et al: Myelination of the human vagus nerve from 24 weeks postconceptional age to adolescence. J Neuropathol Exp Neurol 1982;41:466–472. doi: 10.1097/00005072-198207000-00009

114.
Dash S, Syed YA, Khan MR: Understanding the role of the gut microbiome in brain development and its association with neurodevelopmental psychiatric disorders. Front Cell Dev Biol 2022;10:880544. doi: 10.3389/fcell.2022.880544

115.
Garzoni L, Faure C, Frasch MG: Fetal cholinergic anti-inflammatory pathway and necrotizing enterocolitis: the brain-gut connection begins in utero. Front Integr Neurosci 2013;7:57. doi: 10.3389/fnint.2013.00057

116.
Nyangahu DD, Jaspan HB: Influence of maternal microbiota during pregnancy on infant immunity. Clin Exp Immunol 2019;198:47–56. doi: 10.1111/cei.13331

117.
Nyangahu DD, Lennard KS, Brown BP, et al: Disruption of maternal gut microbiota during gestation alters offspring microbiota and immunity. Microbiome 2018;6:124. doi: 10.1186/s40168-018-0511-7

118.
Joly A, Leulier F, De Vadder F: Microbial modulation of the development and physiology of the enteric nervous system. Trends Microbiol 2021;29(8):686–699. doi: 10.1016/j.tim.2020.11.007

119.
Yang LL, Millischer V, Rodin S, et al: Enteric short-chain fatty acids promote proliferation of human neural progenitor cells. J Neurochem 2020;154:635–646. doi: 10.1111/jnc.14928

120.
Rogers GB, Keating DJ, Young RL, et al: From gut dysbiosis to altered brain function and mental illness: mechanisms and pathways. Mol Psychiatry 2016;21:738–748. doi: 10.1038/mp.2016.50

121.
Warner BB: The contribution of the gut microbiome to neurodevelopment and neuropsychiatric disorders. Pediatr Res 2019;85:216–224. doi: 10.1038/s41390-018-0191-9

122.
Uystepruyst C, Coghe J, Dorts T, et al: Sternal recumbency or suspension by the hind legs immediately after delivery improves respiratory and metabolic adaptation to extra uterine life in newborn calves delivered by caesarean section. Vet Res 2002;33:709–724. doi: 10.1051/vetres:2002051

123.
Uystepruyst C, Coghe J, Dorts T, et al: Effect of three resuscitation procedures on respiratory and metabolic adaptation to extra uterine life in newborn calves. Vet J 2002;163:30–44. doi: 10.1053/tvjl.2001.0633

124.
Armstrong L, Caulkett N, Pearson JM, et al: Assessing the efficacy of ventilation of anesthetized neonatal calves using a laryngeal mask airway or mask resuscitator. Front Vet Sci 2018;5:292. doi: 10.3389/fvets.2018.00292

125.
Di Gesù CM, Matz LM, Buffington SA: Diet-induced dysbiosis of the maternal gut microbiome in early life programming of neurodevelopmental disorders. Neurosci Res 2021;168:3–19. doi: 10.1016/j.neures.2021.05.003

126.
Kim SW, Youk T, Kim J: Maternal and neonatal risk factors affecting the occurrence of neurodevelopmental disorders: a population-based nationwide study. Asia Pac J Public Health 2022;34:199–205. doi: 10.1177/10105395211066383

127.
Bleul U, Bircher B, Jud RS, et al: Respiratory and cardiovascular effects of doxapram and theophylline for the treatment of asphyxia in neonatal calves. Theriogenology 2010;73:612–619. doi: 10.1016/j.theriogenology.2009.10.017

128.
Bleul U, Bylang T: Effects of doxapram, prethcamide and lobeline on spirometric, blood gas and acid-base variables in healthy new-born calves. Vet J 2012;194:240–246. doi: 10.1016/j.tvjl.2012.04.007

129.
Constable PD, Trefz FM, Sen I, et al: Intravenous and oral fluid therapy in neonatal calves with diarrhea or sepsis and in adult cattle. Front Vet Sci 2021;7:603358. doi: 10.3389/fvets.2020.603358

130.
Shankaran S, Laptook AR, Ehrenkranz RA, et al: Whole-body hypothermia for neonates with hypoxic-ischemic encephalopathy. N Engl J Med 2005;353:1574–1584. doi: 10.1056/NEJMcps050929

131.
Godden SM, Lombard JE, Woolums AR: Colostrum management for dairy calves. Vet Clin North Am Food Anim Pract 2019;35:535–556. doi: 10.1016/j.cvfa.2019.07.005

132.
Abdelfattah E, Fausak E, Maier G: Failure of passive immune transfer in neonatal beef calves: A scoping review. Animals (Basel) 2025;15:2072. doi: 10.3390/ani15142072
Published
2026-04-07
How to Cite
Bailey , B., & Kasimanickam , R. (2026). Neurologic dysfunction in newborn calves: understanding neonatal encephalopathy in clinical practice. Clinical Theriogenology, 18. https://doi.org/10.58292/CT.v18.13247
Section
Review Reports