Cellular mechanisms mediating rat renal microvascular constriction by angiotensin II

Tsuneo Takenaka, Hiromichi Suzuki, Keiji Fujiwara, Yoshihiko Kanno, Yoichi Ohno, Koichi Hayashi, Takahiko Nagahama, Takao Saruta

研究成果: Article

49 引用 (Scopus)

抄録

To assess cellular mechanisms mediating afferent (AA) and efferent arteriolar (EA) constriction by angiotensin II (AngII), experiments were performed using isolated perfused hydronephrotic kidneys. In the first series of studies, AngII (0.3 nM) constricted AAs and EAs by 29±3 (n = 8, P < 0.01) and 27±3% (n = 8, P < 0.01), respectively. Subsequent addition of nifedipine restored AA but not EA diameter. Manganese (8 mM) reversed EA constriction by 65±9% (P < 0.01). In the second group, the addition of N-ethylmaleimide (10 μM), a Gi/Go protein antagonist, abolished AngII-induced EA (n = 6) but not AA constriction (n = 6). In the third series of experiments, treatment with 2-nitro-4-carboxyphenyl-N,N-diphenyl-carbamate (200 μM), a phospholipase C inhibitor, blocked both AA and EA constriction by AngII (n = 6 for each). In the fourth group, thapsigargin (1 μM) prevented AngII-induced AA constriction (n = 8) and attenuated EA constriction (8±2% decrease in EA diameter at 0.3 nM AngII, n = 8, P < 0.05). Subsequent addition of manganese (8 mM) reversed EA constriction. Our data provide evidence that in AAs, AngII stimulates phospholipase C with subsequent calcium mobilization that is required to activate voltage-dependent calcium channels. Our results suggest that AngII constricts EAs by activating phospholipase C via the Gi protein family, thereby eliciting both calcium mobilization and calcium entry.

元の言語English
ページ(範囲)2107-2114
ページ数8
ジャーナルJournal of Clinical Investigation
100
発行部数8
出版物ステータスPublished - 1997 10 15

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Constriction
Angiotensin II
Kidney
Type C Phospholipases
Manganese
Calcium
Ethylmaleimide
Thapsigargin
Carbamates
Calcium Channels
Nifedipine
Proteins

ASJC Scopus subject areas

  • Medicine(all)

これを引用

Takenaka, T., Suzuki, H., Fujiwara, K., Kanno, Y., Ohno, Y., Hayashi, K., ... Saruta, T. (1997). Cellular mechanisms mediating rat renal microvascular constriction by angiotensin II. Journal of Clinical Investigation, 100(8), 2107-2114.

Cellular mechanisms mediating rat renal microvascular constriction by angiotensin II. / Takenaka, Tsuneo; Suzuki, Hiromichi; Fujiwara, Keiji; Kanno, Yoshihiko; Ohno, Yoichi; Hayashi, Koichi; Nagahama, Takahiko; Saruta, Takao.

:: Journal of Clinical Investigation, 巻 100, 番号 8, 15.10.1997, p. 2107-2114.

研究成果: Article

Takenaka, T, Suzuki, H, Fujiwara, K, Kanno, Y, Ohno, Y, Hayashi, K, Nagahama, T & Saruta, T 1997, 'Cellular mechanisms mediating rat renal microvascular constriction by angiotensin II', Journal of Clinical Investigation, 巻. 100, 番号 8, pp. 2107-2114.
Takenaka T, Suzuki H, Fujiwara K, Kanno Y, Ohno Y, Hayashi K その他. Cellular mechanisms mediating rat renal microvascular constriction by angiotensin II. Journal of Clinical Investigation. 1997 10 15;100(8):2107-2114.
Takenaka, Tsuneo ; Suzuki, Hiromichi ; Fujiwara, Keiji ; Kanno, Yoshihiko ; Ohno, Yoichi ; Hayashi, Koichi ; Nagahama, Takahiko ; Saruta, Takao. / Cellular mechanisms mediating rat renal microvascular constriction by angiotensin II. :: Journal of Clinical Investigation. 1997 ; 巻 100, 番号 8. pp. 2107-2114.
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AU - Takenaka, Tsuneo

AU - Suzuki, Hiromichi

AU - Fujiwara, Keiji

AU - Kanno, Yoshihiko

AU - Ohno, Yoichi

AU - Hayashi, Koichi

AU - Nagahama, Takahiko

AU - Saruta, Takao

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N2 - To assess cellular mechanisms mediating afferent (AA) and efferent arteriolar (EA) constriction by angiotensin II (AngII), experiments were performed using isolated perfused hydronephrotic kidneys. In the first series of studies, AngII (0.3 nM) constricted AAs and EAs by 29±3 (n = 8, P < 0.01) and 27±3% (n = 8, P < 0.01), respectively. Subsequent addition of nifedipine restored AA but not EA diameter. Manganese (8 mM) reversed EA constriction by 65±9% (P < 0.01). In the second group, the addition of N-ethylmaleimide (10 μM), a Gi/Go protein antagonist, abolished AngII-induced EA (n = 6) but not AA constriction (n = 6). In the third series of experiments, treatment with 2-nitro-4-carboxyphenyl-N,N-diphenyl-carbamate (200 μM), a phospholipase C inhibitor, blocked both AA and EA constriction by AngII (n = 6 for each). In the fourth group, thapsigargin (1 μM) prevented AngII-induced AA constriction (n = 8) and attenuated EA constriction (8±2% decrease in EA diameter at 0.3 nM AngII, n = 8, P < 0.05). Subsequent addition of manganese (8 mM) reversed EA constriction. Our data provide evidence that in AAs, AngII stimulates phospholipase C with subsequent calcium mobilization that is required to activate voltage-dependent calcium channels. Our results suggest that AngII constricts EAs by activating phospholipase C via the Gi protein family, thereby eliciting both calcium mobilization and calcium entry.

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KW - Calcium mobilization

KW - Glomerular arteriole

KW - GTP-binding protein

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