Anxiogenic role of vasopressin during the early postnatal period: maternal separation-induced ultrasound vocalization in vasopressin-deficient Brattleboro rats

Amino Acids ◽  
2015 ◽  
Vol 47 (11) ◽  
pp. 2409-2418 ◽  
Author(s):  
János Varga ◽  
Anna Fodor ◽  
Barbara Klausz ◽  
Dóra Zelena
Stress ◽  
2016 ◽  
Vol 19 (4) ◽  
pp. 434-438 ◽  
Author(s):  
Diána Balázsfi ◽  
Lívia Farkas ◽  
Péter Csikota ◽  
Anna Fodor ◽  
Sándor Zsebők ◽  
...  

Endocrinology ◽  
2008 ◽  
Vol 149 (5) ◽  
pp. 2576-2583 ◽  
Author(s):  
Dóra Zelena ◽  
Ágnes Domokos ◽  
István Barna ◽  
Zsuzsa Mergl ◽  
József Haller ◽  
...  

In adulthood the hypothalamo-pituitary-adrenal axis is controlled by both CRH and arginine vasopressin (AVP). However, in neonates CRH secretion is very low, whereas AVP secretion is fully functional. This suggests that the role of AVP is more pronounced in young than in adult rats. We investigated the role of AVP by studying stress responses in 5, 10, and 20-d-old AVP-deficient Brattleboro rats. Two different stressors were applied: 24-h maternal separation and Hypnorm Grove Oxford UK injections. In heterozygous controls (that do express AVP), both stressors increased plasma ACTH and corticosterone. The ACTH stress response disappeared in AVP-deficient rats, demonstrating that during the perinatal period, the secretion of this hormone is controlled by AVP. Surprisingly, corticosterone responses remained intact in AVP-deficient rats. Similar findings were obtained after 1-, 4-, 12-, and 24-h long maternal separations. Thus, preserved corticosterone stress responses were not explained by changes in the timing of ACTH secretion. In vitro experiments suggested that the dissociation of ACTH and corticosterone stress responses can only be partly explained by higher ACTH responsiveness of the adrenal cortex in AVP-deficient rats. Together, our results show that in neonatal periods, AVP is crucial for the expression of ACTH stress responses, but neither AVP nor ACTH is necessary for the induction of corticosterone stress responses. Discrepant ACTH and corticosterone stress responses may reflect compensatory mechanisms activated by AVP deficiency, but disparate findings suggest that they rather depict a neonate-specific mechanism of hypothalamo-pituitary-adrenal-axis control.


2021 ◽  
Vol 22 (11) ◽  
pp. 6037
Author(s):  
Dina K. Gaynullina ◽  
Tatiana V. Kudryashova ◽  
Alexander V. Vorotnikov ◽  
Rudolf Schubert ◽  
Olga S. Tarasova

Previously, the abundance of p42/44 and p38 MAPK proteins had been shown to be higher in arteries of 1- to 2-week-old compared to 2- to 3-month-old rats. However, the role of MAPKs in vascular tone regulation in early ontogenesis remains largely unexplored. We tested the hypothesis that the contribution of p42/44 and p38 MAPKs to the contraction of peripheral arteries is higher in the early postnatal period compared to adulthood. Saphenous arteries of 1- to 2-week-old and 2- to 3-month-old rats were studied using wire myography and western blotting. The α1-adrenoceptor agonist methoxamine did not increase the phosphorylation level of p38 MAPK in either 1- to 2-week-old or 2- to 3-month-old rats. Accordingly, inhibition of p38 MAPK did not affect arterial contraction to methoxamine in either age group. Methoxamine increased the phosphorylation level of p42/44 MAPKs in arteries of 2- to 3-month-old and of p44 MAPK in 1- to 2-week-old rats. Inhibition of p42/44 MAPKs reduced methoxamine-induced contractions in arteries of 2- to 3-month-old, but not 1- to 2-week-old rats. Thus, despite a high abundance in arterial tissue, p38 and p42/44 MAPKs do not regulate contraction of the saphenous artery in the early postnatal period. However, p42/44 MAPK activity contributes to arterial contractions in adult rats.


2016 ◽  
Vol 38 ◽  
pp. 69-73 ◽  
Author(s):  
Melissa Hines ◽  
Debra Spencer ◽  
Karson TF Kung ◽  
Wendy V Browne ◽  
Mihaela Constantinescu ◽  
...  

2019 ◽  
Vol 81 (10) ◽  
pp. 1461-1467 ◽  
Author(s):  
Ayumi TSUBOTA ◽  
Yuko OKAMATSU-OGURA ◽  
Jussiaea Valente BARIUAN ◽  
Junnosuke MAE ◽  
Shinya MATSUOKA ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Katsuya Uchida ◽  
Kentaro Hasuoka ◽  
Toshimitsu Fuse ◽  
Kenichi Kobayashi ◽  
Takahiro Moriya ◽  
...  

AbstractThe functional role of thyroid hormone (TH) in the cortex and hippocampus of mouse during neuronal development was investigated in this study. TH insufficiency showed a decrease in the expression of parvalbumin (PV) in the cortex and hippocampus of pups at postnatal day (PD) 14, while treatment with thyroxine from PD 0 to PD 14 ameliorated the PV loss. On the other hand, treatment with antithyroid agents in adulthood did not result in a decrease in the expression of PV in these areas. These results indicate the existence of a critical period of TH action during the early postnatal period. A decrease in MeCP2-positive neuronal nuclei was also observed in the cortical layers II–IV of the cerebral cortex. The brains were then stained with CUX1, a marker for cortical layers II–IV. In comparison with normal mice, CUX1 signals were decreased in the somatosensory cortex of the hypothyroid mice, and the total thickness of cortical layers II–IV of the mice was lower than that of normal mice. These results suggest that TH insufficiency during the perinatal period strongly and broadly affects neuronal development.


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