Brain Endoplasmic Reticulum Stress Mechanistically Distinguishes the Saline-Intake and Hypertensive Response to Deoxycorticosterone Acetate–Salt

• Published in: Hypertension (Dallas, Tex. 1979) Tex. 1979), 2015-06, Vol.65 (6), p.1341-1348
• Main Authors: Jo, Fusakazu, Jo, Hiromi, Hilzendeger, Aline M, Thompson, Anthony P, Cassell, Martin D, Rutkowski, D Thomas, Davisson, Robin L, Grobe, Justin L, Sigmund, Curt D
• Format: Article
• Language: English
• Subjects: Analysis of Variance; Animals; Blood Pressure - drug effects; Brain - metabolism; Desoxycorticosterone Acetate - pharmacology; Disease Models, Animal; Endoplasmic Reticulum Stress - drug effects; Endoplasmic Reticulum Stress - physiology; Hypertension - physiopathology; Infusions, Intraventricular; Mice; Mice, Inbred C57BL; Random Allocation; Reference Values; Sensitivity and Specificity; Sodium Chloride - metabolism; Sodium Chloride - pharmacology; Statistics, Nonparametric; Subfornical Organ - drug effects; Subfornical Organ - physiopathology
• ISSN: 0194-911X; 1524-4563
• DOI: 10.1161/HYPERTENSIONAHA.115.05377

Endoplasmic reticulum stress has become an important mechanism in hypertension. We examined the role of endoplasmic reticulum stress in mediating the increased saline-intake and hypertensive effects in response to deoxycorticosterone acetate (DOCA)–salt. Intracerebroventricular delivery of the endoplasmic reticulum stress–reducing chemical chaperone tauroursodeoxycholic acid did not affect the magnitude of hypertension, but markedly decreased saline-intake in response to DOCA-salt. Increased saline-intake returned after tauroursodeoxycholic acid was terminated. Decreased saline-intake was also observed after intracerebroventricular infusion of 4-phenylbutyrate, another chemical chaperone. Immunoreactivity to CCAAT homologous binding protein, a marker of irremediable endoplasmic reticulum stress, was increased in the subfornical organ and supraoptic nucleus of DOCA-salt mice, but the signal was absent in control and CCAAT homologous binding protein–deficient mice. Electron microscopy revealed abnormalities in endoplasmic reticulum structure (decrease in membrane length, swollen membranes, and decreased ribosome numbers) in the subfornical organ consistent with endoplasmic reticulum stress. Subfornical organ-targeted adenoviral delivery of GRP78, a resident endoplasmic reticulum chaperone, decreased DOCA-salt–induced saline-intake. The increase in saline-intake in response to DOCA-salt was blunted in CCAAT homologous binding protein–deficient mice, but these mice exhibited a normal hypertensive response. We conclude that (1) brain endoplasmic reticulum stress mediates the saline-intake, but not blood pressure response to DOCA-salt, (2) DOCA-salt causes endoplasmic reticulum stress in the subfornical organ, which when attenuated by GRP78 blunts saline-intake, and (3) CCAAT homologous binding protein may play a functional role in DOCA-salt–induced saline-intake. The results suggest a mechanistic distinction between the importance of endoplasmic reticulum stress in mediating effects of DOCA-salt on saline-intake and blood pressure.