タナカ ヨシオ   Tanaka Yoshio
  田中 芳夫
   所属   東邦大学  薬学部 薬学科
   職種   教授
論文種別 原著
言語種別 英語
査読の有無 査読あり
表題 The nitric oxide-cGMP pathway does not play an essential role in β-adrenoceptor-mediated smooth muscle direct relaxation in the rat thoracic aorta
掲載誌名 正式名:Toho Journal of Medicine
掲載区分国内
出版社 東邦医学会
巻・号・頁 2(3),pp.95-105
著者・共著者 Shiina S†, Ui R†, Endo T†, Obara K†, Chino D†, Tanaka Y*†
担当区分 最終著者,責任著者
発行年月 2016/09
概要 Background: The smooth muscles of blood vessels express relaxant β-adrenoceptor, which functions as a negative feed-back system against α1-adrenoceptor-mediated contraction. Although β-adrenoceptor-mediated vascular smooth relaxation is generally thought to be triggered through a cAMP-dependent pathway, a recent report has suggested a principal role for the nitric oxide (NO)-cGMP pathway. Thus, in this study, we examined whether the NO-cGMP pathway played an essential role in β-adrenoceptor-mediated smooth muscle direct relaxation in the rat thoracic aorta.
Methods: The effects of an NO synthase inhibitor (L-NNA) or a soluble guanylyl cyclase inhibitor (ODQ) on the relaxation responses to β-adrenoceptor agonists were examined in endothelium-denuded rat thoracic aortas. The effects of β-adrenoceptor agonists on arterial cGMP content were also examined.
Results: Both L-NNA and ODQ potently suppressed acetylcholine (ACh)-induced, endothelium-dependent relaxation. ODQ also largely suppressed endothelium-independent relaxation induced by an NO donor ((±)-(E)-4-ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide [NOR3]). However, relaxation of the endothelium-denuded aortas in response to the β-adrenoceptor agonists isoprenaline, salbutamol, isoprenaline or CGP-12177A in the presence of propranolol, or noradrenaline was not substantially reduced by L-NNA or ODQ. Neither isoprenaline nor noradrenaline affected arterial cGMP content, whereas NOR3 caused an approximately 30-fold increase in cGMP content.
Conclusions: Our findings suggested that the NO-cGMP pathway had an insignificant effect on endothelium-independent smooth muscle direct relaxation in the rat thoracic aorta in response to β-adrenoceptor agonists of any subtype (β1, β2, or β3).