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妥拉唑啉和硝普钠对人离体桡动脉的比较效应

Comparative effects of tolazoline and nitroprusside on human isolated radial artery.

作者信息

Teskin Onder, Uydeş-Dogan B Sönmez, Enç Yavuz, Alp F Ilkay, Kaleli Deniz, Keser Süheyla, Iyigün Taner, Bilgen Fuat, Dagsali Sabri, Ozdemir Osman

机构信息

Department of Cardiovascular Surgery, Siyami Ersek Thoracic and Cardiovascular Surgery Education and Research Hospital, Istanbul, Turkey.

出版信息

Ann Thorac Surg. 2006 Jan;81(1):125-31. doi: 10.1016/j.athoracsur.2005.07.020.

Abstract

BACKGROUND

The radial artery is increasingly being used in coronary revascularization as an alternative conduit to a saphenous vein graft. Its perfect endothelial capacity provides a high patency rate comparable with the internal mammary artery (IMA). However, its spastic characteristics cause difficulties during its intraoperative preparation and may lead to early postoperative graft failure. Thus, treatment and/or prevention of radial artery spasm with an effective vasodilator agent is essential for its longevity. Endogenous vasoconstrictors, including noradrenaline, endothelin-1, and thromboxane A2, are likely to play a role in the pathogenesis of graft spasm. In the present study, we evaluated the vasorelaxant effect of tolazoline, a nonselective alpha-adrenoceptor blocker, against the contractions induced by various spasmogenic agents in an isolated human radial artery.

METHODS

Tolazoline (10(-9)-10(-4) M) or sodium nitroprusside (SNP, 10(-9)-10(-4) M) were cumulatively applied on radial artery rings precontracted submaximally with noradrenaline, endothelin-1, thromboxane analogue, U46619, or potassium chloride. In addition, some rings were pretreated with tolazoline (4 x 10(-6) M) for 30 minutes and the contractile response curve to noradrenaline was assessed in its presence.

RESULTS

Tolazoline effectively reversed noradrenaline-induced contractions in the radial artery, whereas it failed to produce remarkable relaxations on rings contracted with other spasmogenic agents, while SNP overcame the contractions induced by all spasmogens to a similar extent. In addition, brief pretreatment of radial artery rings with tolazoline significantly inhibited the contractions to noradrenaline.

CONCLUSIONS

Tolazoline is not as broadly effective as SNP against all spasmogens investigated; however, it may be effective in counteracting alpha-adrenoceptor-mediated vasospasm in human radial arteries.

摘要

背景

桡动脉越来越多地被用于冠状动脉血运重建,作为大隐静脉移植的替代管道。其完美的内皮功能使其通畅率高,可与乳内动脉(IMA)相媲美。然而,其痉挛特性在术中制备时会造成困难,并可能导致术后早期移植失败。因此,用有效的血管扩张剂治疗和/或预防桡动脉痉挛对其长期通畅至关重要。内源性血管收缩剂,包括去甲肾上腺素、内皮素-1和血栓素A2,可能在移植痉挛的发病机制中起作用。在本研究中,我们评估了非选择性α-肾上腺素受体阻滞剂妥拉唑啉对离体人桡动脉中各种致痉剂诱导的收缩的血管舒张作用。

方法

将妥拉唑啉(10⁻⁹ - 10⁻⁴ M)或硝普钠(SNP,10⁻⁹ - 10⁻⁴ M)累积应用于用去甲肾上腺素、内皮素-1、血栓素类似物U46619或氯化钾预收缩至亚最大程度 的桡动脉环。此外,一些环用妥拉唑啉(4×10⁻⁶ M)预处理30分钟,并在其存在的情况下评估对去甲肾上腺素的收缩反应曲线。

结果

妥拉唑啉有效地逆转了去甲肾上腺素诱导的桡动脉收缩,而它对用其他致痉剂收缩的环未能产生明显的舒张作用,而SNP在相似程度上克服了所有致痉剂诱导的收缩。此外,用妥拉唑啉对桡动脉环进行短暂预处理可显著抑制对去甲肾上腺素的收缩。

结论

妥拉唑啉对所研究的所有致痉剂不如SNP具有广泛的有效性;然而,它可能有效地对抗人桡动脉中α-肾上腺素受体介导的血管痉挛。

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