Vascular Aldosterone in Genetically Hypertensive Rats

Author:

Takeda Yoshiyu1,Miyamori Isamu1,Inaba Satoru1,Furukawa Kenji1,Hatakeyama Haruhiko1,Yoneda Takashi1,Mabuchi Hiroshi1,Takeda Ryoyu1

Affiliation:

1. the Second Department of Internal Medicine (Y.T., I.M., S.I., K.F., H.H., T.Y., H.M.) and Department of Health Sciences (Y.T.), School of Medicine, Kanazawa University, and KKR Hokuriku Hospital (R.T.), Kanazawa, Japan.

Abstract

We have reported that aldosterone is synthesized and cytochrome P450aldo mRNA exists in the vasculature. To clarify the pathophysiological role of vascular aldosterone in hypertension, we compared aldosterone production in the mesenteric arteries of stroke-prone spontaneously hypertensive rats (SHRSP) with that in Wistar-Kyoto rats (WKY). The expressions of mRNA of cytochrome P450aldo, mineralocorticoid receptor, and α 1 Na,K-ATPase in the mesenteric arteries were compared between the two groups. Aldosterone concentration in the perfusate of the vasculature was measured by radioimmunoassay after purification with high-performance liquid chromatography. Cytochrome P450aldo and mineralocorticoid receptor mRNA levels were quantified by Southern blot analysis of the products of reverse-transcribed polymerase chain reaction. Levels of α 1 Na,K-ATPase mRNA were measured by Northern blot analysis. Vascular aldosterone and cytochrome P450aldo mRNA levels of 2-week-old SHRSP were significantly increased compared with those of age-matched WKY. However, vascular aldosterone in 4- and 9-week-old SHRSP did not differ from that in age-matched WKY. Expression levels of mineralocorticoid receptor mRNA in the vasculature of 4- and 9-week-old SHRSP were significantly increased compared with those in age-matched WKY. Concentrations of vascular α 1 Na,K-ATPase mRNA of 2-, 4-, and 9-week-old SHRSP also were significantly higher than those in age-matched WKY. These results suggest that vascular aldosterone contributes to the pathophysiology of hypertension in SHRSP in the early stage.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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