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Endoplasmic reticulum stress in the brain subfornical organ contributes to sex differences in angiotensin‐dependent hypertension in rats
Author(s) -
Dai S.Y.,
Fan J.,
Shen Y.,
He J.J.,
Peng W.
Publication year - 2016
Publication title -
acta physiologica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.591
H-Index - 116
eISSN - 1748-1716
pISSN - 1748-1708
DOI - 10.1111/apha.12635
Subject(s) - endocrinology , subfornical organ , medicine , ovariectomized rat , angiotensin ii , tunicamycin , endoplasmic reticulum , blood pressure , renin–angiotensin system , saline , unfolded protein response , hormone , biology , biochemistry
Aim Endoplasmic reticulum ( ER ) stress in the brain subfornical organ ( SFO ), a key cardiovascular regulatory centre, has been implicated in angiotensin ( ANG ) II ‐induced hypertension in males; however, the contribution of ER stress to ANG II ‐induced hypertension in females is unknown. Female hormones have been shown to prevent ER stress in the periphery. We tested the hypothesis that females are less susceptible to ANG II ‐induced SFO ER stress than males, leading to sex differences in hypertension. Methods Male, intact and ovariectomized ( OVX ) female rats received a continuous 2‐week subcutaneous infusion of ANG II or saline. Additional male, intact and OVX female rats received intracerebroventricular ( ICV ) injection of ER stress inducer tunicamycin. Results ANG II , but not saline, increased blood pressure ( BP ) in both males and females, but intact females exhibited smaller increase in BP and less depressor response to ganglionic blockade compared with males or OVX females. Molecular studies revealed that ANG II elevated expression of ER stress biomarkers and Fra‐like activity in the SFO in both males and females; however, elevations in these parameters were less in intact females than in males or OVX females. Moreover, ICV tunicamycin induced smaller elevation in BP and less increase in expression of ER stress biomarkers in the SFO in intact females compared with males or OVX females. Conclusion The results suggest that differences in ANG II ‐induced brain ER stress between males and females contribute to sex differences in ANG II ‐mediated hypertension and that oestrogen protects females against ANG II ‐induced brain ER stress.