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Prenatal immobilization stress and postnatal maternal separation cause differential neuroendocrine responses to fasting stress in adult male rats
Author(s) -
Roque Angélica,
RuizGonzález Roberto,
Pineda-López Edel,
Torner Luz,
Lajud Naima
Publication year - 2020
Publication title -
developmental psychobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 93
eISSN - 1098-2302
pISSN - 0012-1630
DOI - 10.1002/dev.21947
Subject(s) - endocrinology , medicine , corticosterone , maternal deprivation , stressor , prenatal stress , hypothalamus , elevated plus maze , anxiety , corticotropin releasing hormone , hormone , psychology , pregnancy , gestation , biology , neuroscience , genetics , psychiatry
Prenatal immobilization stress (PNS) and postnatal maternal separation (MS180) are two widely used rodent models of early‐life stress (ELS) that affect the hypothalamus–pituitary–adrenal (HPA) axis, cause behavioral alterations, and affect glucose tolerance in adults. We compared anxiety‐like behavior, coping strategies, and HPA axis activity in PNS and MS180 adult (4‐month‐old) male rats and assessed their glucose tolerance and HPA axis response after mild fasting stress. Both PNS and MS180 induced a passive coping strategy in the forced swimming test, without affecting anxiety‐like behavior in the elevated plus‐maze. Moreover, both PNS and MS180 increased the hypothalamic corticotropin‐releasing hormone expression; however, only MS180 increased the circulating corticosterone levels. Both early life stressors increased fasting glucose levels and this effect was significantly higher in PNS rats. MS180 rats showed impaired glucose tolerance 120 min after intravenous glucose administration, whereas PNS rats displayed an efficient homeostatic response. Moreover, MS180 rats showed higher circulating corticosteroid levels in response to fasting stress (overnight fasting, 12 hr), which were restored after glucose administration. In conclusion, early exposure to postnatal MS180, unlike PNS, increases the HPA axis response to moderate fasting stress, indicating a differential perception of fasting as a stressor in these two ELS models.