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鱼油和n-3二十碳五烯酸会影响血管平滑肌细胞的细胞内游离钙浓度和血栓素A2的形成。

Intracellular free calcium concentration and thromboxane A2 formation of vascular smooth muscle cells are influenced by fish oil and n-3 eicosapentaenoic acid.

作者信息

Locher R, Sachinidis A, Brunner C, Vetter W

机构信息

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

出版信息

Scand J Clin Lab Invest. 1991 Oct;51(6):541-7. doi: 10.3109/00365519109104563.

Abstract

UNLABELLED

The effect of fish oil and n-3 eicosapentaenoic acid (EPA) on intracellular free calcium concentration ([Ca2+]i) and thromboxane B2 (TXB2) formation in resting and stimulated cultured rat vascular smooth muscle cells (VSMC) was examined. In resting control cells [Ca2+]i was 147 +/- 15 nmol l-1 (mean +/- SEM, n = 4). After pretreatment of the cells with fish oil or EPA for 24 days the resting [Ca2+]i was decreased to 126 +/- 10 nmol l-1 and 84 +/- 8 nmol-1, respectively. After stimulation of untreated control cells with either 100 nmol l-1 angiotensin II (AII), 40 micrograms ml-1 low-density lipoprotein (LDL), or 100 ng ml-1 of recombinant platelet-derived growth factor (PDGFAB), [Ca2+]i was (in nmol l-1) 306 +/- 31, 217 +/- 25 and 213 +/- 16. Treatment of cells with fish oil or EPA reduced the stimulatory effect of the agonists, and the following [Ca2+]i values (in nmol l-1) were found: 199 +/- 21, 131 +/- 10, 148 +/- 13; and 175 +/- 11, 98 +/- 12, and 103 +/- 6, respectively. PDGFAB induced a four fold increase in TXB2-generation (270 +/- 28 pg mg-1 cell protein compared with 61 +/- 8.2 pg mg-1 in unstimulated control cells) within 6 min. In cells pretreated with fish oil or EPA, TXB2-formation was reduced by 54% and 44%, respectively.

IN CONCLUSION

in rat VSMC stimulated by a variety of vasoactive agonist, fish oil and EPA can markedly attenuate intracellular mechanisms related to changes of cytosolic calcium concentration and eicosanoid production.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

未标记

研究了鱼油和n-3二十碳五烯酸(EPA)对静息和刺激的培养大鼠血管平滑肌细胞(VSMC)内游离钙浓度([Ca2+]i)和血栓素B2(TXB2)形成的影响。在静息对照细胞中,[Ca2+]i为147±15 nmol/L(平均值±标准误,n = 4)。用鱼油或EPA预处理细胞24天后,静息[Ca2+]i分别降至126±10 nmol/L和84±8 nmol/L。用100 nmol/L血管紧张素II(AII)、40 μg/ml低密度脂蛋白(LDL)或100 ng/ml重组血小板衍生生长因子(PDGFAB)刺激未处理的对照细胞后,[Ca2+]i(单位:nmol/L)分别为306±31、217±25和213±16。用鱼油或EPA处理细胞可降低激动剂的刺激作用,得到以下[Ca2+]i值(单位:nmol/L):分别为199±21、131±10、148±13;以及175±11、98±12和103±6。PDGFAB在6分钟内使TXB2生成增加了四倍(与未刺激的对照细胞中61±8.2 pg/mg细胞蛋白相比,为270±28 pg/mg细胞蛋白)。在用鱼油或EPA预处理的细胞中,TXB2形成分别减少了54%和44%。

结论

在多种血管活性激动剂刺激的大鼠VSMC中,鱼油和EPA可显著减弱与胞质钙浓度变化和类花生酸产生相关的细胞内机制。(摘要截短至250字)

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