Suppr超能文献

鱼油影响培养的血管平滑肌细胞中的磷酸肌醇代谢和血栓素A代谢。

Fish oil affects phosphoinositide turnover and thromboxane A metabolism in cultured vascular muscle cells.

作者信息

Locher R, Sachinidis A, Steiner A, Vogt E, Vetter W

机构信息

Department of Internal Medicine, University Hospital, Zürich, Switzerland.

出版信息

Biochim Biophys Acta. 1989 Aug 15;1012(3):279-83. doi: 10.1016/0167-4889(89)90109-2.

Abstract

Fish oil has been reported as having beneficial effects on cardiovascular diseases. Elevated serum lipoproteins, prostaglandins and intracellular free calcium concentrations [( Ca2+]i) of the vasculature and thus the phosphoinositide (PI) turnover may be involved in the pathogenesis of these disorders. Therefore, the effect of fish oil on the potency of both low-density lipoprotein (LDL) and angiotensin II (AII) to stimulate the PI turnover in cultured rat vascular smooth muscle cells (VSMC) has been studied. Furthermore, a possible link between PI turnover activity and thromboxane A2 (TXA2) metabolism in these cells has been investigated. In VSMC cultured for up to 7 weeks with either fish oil or n-3 eicosapentaenoic acid (EPA) a decrease to 5-48% of the LDL-induced inositol trisphosphate (IP3) formation (= 100%) was found. A similar range of decreased IP3 synthesis was observed, when AII was used instead of LDL. Both LDL- and AII-stimulated TXA2 synthesis was suppressed concomitantly within the range 34-60%. Blockade of VSMC TXA2 biosynthesis with either indomethacin or TXA2 synthetase blocker (SQ-80338) inhibited LDL-induced formation of IP3 in a dose-dependent manner. Similar results were obtained, when TXA2 receptor coupling antagonists (SQ-27427 or BM-13177) were used. However, blockers of TXA2 synthesis and of TXA2 receptor binding failed to affect AII-induced formation of IP3.

摘要

据报道,鱼油对心血管疾病具有有益作用。血管中血清脂蛋白、前列腺素和细胞内游离钙浓度[(Ca2+]i)升高,进而磷脂酰肌醇(PI)周转可能参与了这些疾病的发病机制。因此,研究了鱼油对低密度脂蛋白(LDL)和血管紧张素II(AII)刺激培养的大鼠血管平滑肌细胞(VSMC)中PI周转能力的影响。此外,还研究了这些细胞中PI周转活性与血栓素A2(TXA2)代谢之间的可能联系。在用鱼油或n-3二十碳五烯酸(EPA)培养长达7周的VSMC中,发现LDL诱导的肌醇三磷酸(IP3)形成(=100%)降低至5-48%。当使用AII代替LDL时,观察到IP3合成有类似程度的降低。LDL和AII刺激的TXA2合成均在34-60%的范围内同时受到抑制。用吲哚美辛或TXA2合成酶阻滞剂(SQ-80338)阻断VSMC的TXA2生物合成,以剂量依赖的方式抑制LDL诱导的IP3形成。当使用TXA2受体偶联拮抗剂(SQ-27427或BM-13177)时,获得了类似的结果。然而,TXA2合成阻滞剂和TXA2受体结合阻滞剂未能影响AII诱导的IP3形成。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验