Impaired feedback regulation of the receptor activity and the myofilament Ca2+ sensitivity contributes to increased vascular reactiveness after subarachnoid hemorrhage

Yuichiro Kikkawa, Katsuharu Kameda, Mayumi Hirano, Tomio Sasaki, Katsuya Hirano

研究成果: ジャーナルへの寄稿記事

25 引用 (Scopus)

抄録

Cerebral vasospasm determines the prognosis of subarachnoid hemorrhage (SAH). The increased vascular reactiveness has an important role in the development of cerebral vasospasm. This study analyzed the roles of the receptor-mediated signaling and the myofilament Ca 2 sensitivity in the increased vascular reactiveness in SAH, using the basilar artery of a rabbit SAH model. Endothelin-1, thrombin, and phenylephrine induced transient increases in Ca 2 i, myosin light chain phosphorylation, and contraction in the controls. All these responses were not only enhanced but also became sustained in SAH. In the sequential stimulation of thrombin receptor or α 1-adrenoceptor, the second response was substantially attenuated in the controls, whereas it was maintained in SAH. The thrombin-induced contraction in SAH irreversibly persisted even after terminating the thrombin stimulation. This contraction was completely reversed by trypsin and a Gα q inhibitor YM254890, thus suggesting the sustained receptor activity during the sustained contraction. YM254890 also inhibited the endothelin-1- and phenylephrine-induced sustained contraction. Furthermore, the GTPγS-induced transient contraction in the control α-toxin-permeabilized strips was converted to a sustained contraction in SAH. The results provide the first evidence that the feedback inactivation of the receptor activity and the myofilament Ca 2 sensitivity was impaired in SAH, thus contributing to the increased vascular reactiveness.

元の言語英語
ページ(範囲)1637-1650
ページ数14
ジャーナルJournal of Cerebral Blood Flow and Metabolism
30
発行部数9
DOI
出版物ステータス出版済み - 1 1 2010

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Myofibrils
Subarachnoid Hemorrhage
Blood Vessels
Thrombin
Intracranial Vasospasm
Phenylephrine
Endothelin-1
Thrombin Receptors
Basilar Artery
Trypsin
Adrenergic Receptors
Phosphorylation
Rabbits

All Science Journal Classification (ASJC) codes

  • Neurology
  • Clinical Neurology
  • Cardiology and Cardiovascular Medicine

これを引用

Impaired feedback regulation of the receptor activity and the myofilament Ca2+ sensitivity contributes to increased vascular reactiveness after subarachnoid hemorrhage. / Kikkawa, Yuichiro; Kameda, Katsuharu; Hirano, Mayumi; Sasaki, Tomio; Hirano, Katsuya.

:: Journal of Cerebral Blood Flow and Metabolism, 巻 30, 番号 9, 01.01.2010, p. 1637-1650.

研究成果: ジャーナルへの寄稿記事

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abstract = "Cerebral vasospasm determines the prognosis of subarachnoid hemorrhage (SAH). The increased vascular reactiveness has an important role in the development of cerebral vasospasm. This study analyzed the roles of the receptor-mediated signaling and the myofilament Ca 2 sensitivity in the increased vascular reactiveness in SAH, using the basilar artery of a rabbit SAH model. Endothelin-1, thrombin, and phenylephrine induced transient increases in Ca 2 i, myosin light chain phosphorylation, and contraction in the controls. All these responses were not only enhanced but also became sustained in SAH. In the sequential stimulation of thrombin receptor or α 1-adrenoceptor, the second response was substantially attenuated in the controls, whereas it was maintained in SAH. The thrombin-induced contraction in SAH irreversibly persisted even after terminating the thrombin stimulation. This contraction was completely reversed by trypsin and a Gα q inhibitor YM254890, thus suggesting the sustained receptor activity during the sustained contraction. YM254890 also inhibited the endothelin-1- and phenylephrine-induced sustained contraction. Furthermore, the GTPγS-induced transient contraction in the control α-toxin-permeabilized strips was converted to a sustained contraction in SAH. The results provide the first evidence that the feedback inactivation of the receptor activity and the myofilament Ca 2 sensitivity was impaired in SAH, thus contributing to the increased vascular reactiveness.",
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