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3,5-二叔丁基邻苯二酚(DTCAT)对大鼠血管平滑肌的解痉活性机制

Mechanisms of the antispasmodic activity of 3,5-di-t-butyl catechol (DTCAT) on rat vascular smooth muscles.

作者信息

Fusi Fabio, Ferrara Antonella, Sgaragli Giampietro, Saponara Simona

机构信息

Dipartimento di Scienze Biomediche, Università degli Studi di Siena, via A. Moro 2, 53100 Siena, Italy.

出版信息

Eur J Pharmacol. 2007 Apr 30;561(1-3):112-20. doi: 10.1016/j.ejphar.2006.12.025. Epub 2007 Jan 19.

Abstract

In skeletal muscle sarcoplasmic reticulum vesicles, 3,5-di-t-butyl catechol (DTCAT) promotes the release of Ca(2+) through the activation of ryanodine receptor Ca(2+) channels. DTCAT mechanical and electrophysiological effects have now been investigated in rat aorta rings and single tail artery myocytes. Rat aorta rings incubated with either 30 microM ryanodine or 100 microM DTCAT developed tension, which averaged 36% and 7%, respectively, of that induced by phenylephrine. DTCAT reduced concentration-dependently both aorta ring contractions to high K(+) (IC(50)=13.5 microM) and L-type Ba(2+) current (IC(50)=22.0 microM) in isolated myocytes. Tetraethylammonium did not reverse the antispasmodic effect of DTCAT in rings stimulated with either 25 or 60 mM K(+). DTCAT relaxed concentration-dependently phenylephrine-pre-contracted rings with intact endothelium (IC(50)=10.9 microM). This effect was markedly reduced by pre-incubation of rings with 100 microM Nomega-nitro-l-arginine methyl ester. DTCAT antagonised phenylephrine-induced contractions in endothelium-deprived rings, either in the presence or in the absence of ryanodine (IC(50)=18.7 microM and 39.8 microM, respectively). Furthermore, both DTCAT (IC(50)=53.3 microM) and ryanodine reduced significantly the response to phenylephrine in the absence of extracellular Ca(2+). Phenylephrine-stimulated influx of extracellular Ca(2+) was markedly inhibited when tissues were pre-treated with DTCAT (IC(50)=19.0 microM) as well as nifedipine. DTCAT (>100 microM) was also able to antagonise the contractions induced by phorbol 12-myristate, 13-acetate. In conclusion, this is the first demonstration that DTCAT inhibits vascular smooth muscle voltage-operated Ca(2+) channels and promotes the release of endothelial nitric oxide. Ryanodine receptor Ca(2+) channels activation or the impairment of the contractile apparatus by DTCAT seem to play a secondary role in its vascular activity.

摘要

在骨骼肌肌浆网囊泡中,3,5-二叔丁基儿茶酚(DTCAT)通过激活兰尼碱受体Ca(2+)通道促进Ca(2+)的释放。现已在大鼠主动脉环和单尾动脉肌细胞中研究了DTCAT的机械和电生理作用。用30 microM兰尼碱或100 microM DTCAT孵育的大鼠主动脉环产生了张力,分别平均为去氧肾上腺素诱导张力的36%和7%。DTCAT浓度依赖性地降低了分离肌细胞中主动脉环对高K(+)的收缩(IC(50)=13.5 microM)和L型Ba(2+)电流(IC(50)=22.0 microM)。四乙铵不能逆转DTCAT对用25或60 mM K(+)刺激的环的解痉作用。DTCAT浓度依赖性地松弛了用去氧肾上腺素预收缩的完整内皮环(IC(50)=10.9 microM)。用100 microM Nω-硝基-L-精氨酸甲酯预孵育环可显著降低这种作用。DTCAT在有或无兰尼碱的情况下,均能拮抗去氧肾上腺素诱导的去内皮环收缩(IC(50)分别为18.7 microM和39.8 microM)。此外,在无细胞外Ca(2+)时,DTCAT(IC(50)=53.3 microM)和兰尼碱均显著降低了对去氧肾上腺素的反应。当组织用DTCAT(IC(50)=19.0 microM)以及硝苯地平预处理时,去氧肾上腺素刺激的细胞外Ca(2+)内流受到明显抑制。DTCAT(>100 microM)也能够拮抗佛波醇12-肉豆蔻酸酯13-乙酸酯诱导的收缩。总之,这是首次证明DTCAT抑制血管平滑肌电压门控Ca(2+)通道并促进内皮一氧化氮的释放。DTCAT激活兰尼碱受体Ca(2+)通道或损害收缩装置似乎在其血管活性中起次要作用。

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