Impaired isoproterenol-induced hyperpolarization in isolated mesenteric arteries of aged rats

Koji Fujii, Uran Onaka, Kenichi Goto, Abe Isao, Masatoshi Fujishima

研究成果: ジャーナルへの寄稿記事

26 引用 (Scopus)

抄録

Stimulation of vascular β-adrenoceptors leads to membrane hyperpolarization, presumably via the β-adrenoceptor/G(s) protein/adenylate cyclase signaling cascade; the ionic mechanisms of this phenomenon remain unclear. β-Adrenoceptor-mediated vascular relaxation is impaired with aging; however, little is known concerning whether β-adrenoceptor-mediated hyperpolarization is altered with aging. We sought to determine the ionic mechanisms of isoproterenol-induced hyperpolarization in the rat mesenteric resistance artery, as well as the age-related changes in isoproterenol- induced hyperpolarization and their underlying mechanisms. Isoprotereno- induced hyperpolarization was inhibited by high-K+ solution and glibenclamide (10-6 mol/L), an inhibitor of ATP-sensitive K+ channels (K(ATP)), but not by apamin, iberiotoxin, or charybdotoxin, inhibitors of Ca2+-activated K+ channels. Isoproterenol-induced hyperpolarization was markedly less in aged rats (≥24 months) than in adults rats (12 to 20 weeks) (3 x 10-6 tool/L; -3.1 versus -9.9 mV; P<0.001; n=8 to 9). Cholera toxin (10-9 g/mL), all activator of G(s), evoked hyperpolarization only in adult rats. Hyperpolarization to forskolin, a direct activator of adenylate cyclase, was also reduced to some extent in aged rats (10-5 mol/L; -8.8 versus -13 mV; P<0.05; n=6), whereas hyperpolarization to levcromakalim, a K(ATP) opener, was comparable in both groups. These findings suggest that isoproterenol elicits hyperpolarization via an opening of K(ATP) in the rat resistance artery and that isoproterenol-induced hyperpolarization is attenuated in aged rats mainly because of a defective coupling of β- adrenoceptors to adenylate cyclase and partly because of a defect at the level of adenylate cyclase, but not because of an alteration of K(ATP) per se.

元の言語英語
ページ(範囲)222-228
ページ数7
ジャーナルHypertension
34
発行部数2
DOI
出版物ステータス出版済み - 1 1 1999

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Mesenteric Arteries
Isoproterenol
Adrenergic Receptors
Adenylyl Cyclases
Adenosine Triphosphate
Blood Vessels
Cromakalim
Charybdotoxin
Apamin
Calcium-Activated Potassium Channels
Glyburide
Cholera Toxin
Colforsin
Arteries
Membranes

All Science Journal Classification (ASJC) codes

  • Internal Medicine

これを引用

Impaired isoproterenol-induced hyperpolarization in isolated mesenteric arteries of aged rats. / Fujii, Koji; Onaka, Uran; Goto, Kenichi; Isao, Abe; Fujishima, Masatoshi.

:: Hypertension, 巻 34, 番号 2, 01.01.1999, p. 222-228.

研究成果: ジャーナルへの寄稿記事

Fujii, Koji ; Onaka, Uran ; Goto, Kenichi ; Isao, Abe ; Fujishima, Masatoshi. / Impaired isoproterenol-induced hyperpolarization in isolated mesenteric arteries of aged rats. :: Hypertension. 1999 ; 巻 34, 番号 2. pp. 222-228.
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T1 - Impaired isoproterenol-induced hyperpolarization in isolated mesenteric arteries of aged rats

AU - Fujii, Koji

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AU - Fujishima, Masatoshi

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N2 - Stimulation of vascular β-adrenoceptors leads to membrane hyperpolarization, presumably via the β-adrenoceptor/G(s) protein/adenylate cyclase signaling cascade; the ionic mechanisms of this phenomenon remain unclear. β-Adrenoceptor-mediated vascular relaxation is impaired with aging; however, little is known concerning whether β-adrenoceptor-mediated hyperpolarization is altered with aging. We sought to determine the ionic mechanisms of isoproterenol-induced hyperpolarization in the rat mesenteric resistance artery, as well as the age-related changes in isoproterenol- induced hyperpolarization and their underlying mechanisms. Isoprotereno- induced hyperpolarization was inhibited by high-K+ solution and glibenclamide (10-6 mol/L), an inhibitor of ATP-sensitive K+ channels (K(ATP)), but not by apamin, iberiotoxin, or charybdotoxin, inhibitors of Ca2+-activated K+ channels. Isoproterenol-induced hyperpolarization was markedly less in aged rats (≥24 months) than in adults rats (12 to 20 weeks) (3 x 10-6 tool/L; -3.1 versus -9.9 mV; P<0.001; n=8 to 9). Cholera toxin (10-9 g/mL), all activator of G(s), evoked hyperpolarization only in adult rats. Hyperpolarization to forskolin, a direct activator of adenylate cyclase, was also reduced to some extent in aged rats (10-5 mol/L; -8.8 versus -13 mV; P<0.05; n=6), whereas hyperpolarization to levcromakalim, a K(ATP) opener, was comparable in both groups. These findings suggest that isoproterenol elicits hyperpolarization via an opening of K(ATP) in the rat resistance artery and that isoproterenol-induced hyperpolarization is attenuated in aged rats mainly because of a defective coupling of β- adrenoceptors to adenylate cyclase and partly because of a defect at the level of adenylate cyclase, but not because of an alteration of K(ATP) per se.

AB - Stimulation of vascular β-adrenoceptors leads to membrane hyperpolarization, presumably via the β-adrenoceptor/G(s) protein/adenylate cyclase signaling cascade; the ionic mechanisms of this phenomenon remain unclear. β-Adrenoceptor-mediated vascular relaxation is impaired with aging; however, little is known concerning whether β-adrenoceptor-mediated hyperpolarization is altered with aging. We sought to determine the ionic mechanisms of isoproterenol-induced hyperpolarization in the rat mesenteric resistance artery, as well as the age-related changes in isoproterenol- induced hyperpolarization and their underlying mechanisms. Isoprotereno- induced hyperpolarization was inhibited by high-K+ solution and glibenclamide (10-6 mol/L), an inhibitor of ATP-sensitive K+ channels (K(ATP)), but not by apamin, iberiotoxin, or charybdotoxin, inhibitors of Ca2+-activated K+ channels. Isoproterenol-induced hyperpolarization was markedly less in aged rats (≥24 months) than in adults rats (12 to 20 weeks) (3 x 10-6 tool/L; -3.1 versus -9.9 mV; P<0.001; n=8 to 9). Cholera toxin (10-9 g/mL), all activator of G(s), evoked hyperpolarization only in adult rats. Hyperpolarization to forskolin, a direct activator of adenylate cyclase, was also reduced to some extent in aged rats (10-5 mol/L; -8.8 versus -13 mV; P<0.05; n=6), whereas hyperpolarization to levcromakalim, a K(ATP) opener, was comparable in both groups. These findings suggest that isoproterenol elicits hyperpolarization via an opening of K(ATP) in the rat resistance artery and that isoproterenol-induced hyperpolarization is attenuated in aged rats mainly because of a defective coupling of β- adrenoceptors to adenylate cyclase and partly because of a defect at the level of adenylate cyclase, but not because of an alteration of K(ATP) per se.

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