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首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >Differential effects of saturated and unsaturated fatty acids on vascular reactivity in isolated mesenteric and femoral arteries of rats
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Differential effects of saturated and unsaturated fatty acids on vascular reactivity in isolated mesenteric and femoral arteries of rats

机译:饱和和不饱和脂肪酸对大鼠离体肠系膜和股动脉的血管反应性的差异作用

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Free fatty acid (FFA) intake regulates blood pressure and vascular reactivity but its direct effect on contractility of systemic arteries is not well understood. We investigated the effects of saturated fatty acid (SFA, palmitic acid), polyunsaturated fatty acid (PUFA, linoleic acid), and monounsaturated fatty acid (MUFA, oleic acid) on the contractility of isolated mesenteric (MA) and deep femoral arteries (DFA) of Sprague–Dawley rats. Isolated MA and DFA were mounted on a dual wire myograph and phenylephrine (PhE, 1–10 μM) concentration-dependent contraction was obtained with or without FFAs. Incubation with 100 μM of palmitic acid significantly increased PhE-induced contraction in both arteries. In MA, treatment with 100 μM of linoleic acid decreased 1 μM PhE-induced contraction while increasing the response to higher PhE concentrations. In DFA, linoleic acid slightly decreased PhE-induced contraction while 200 μM oleic acid significantly decreased it. In MA, oleic acid reduced contraction at low PhE concentration (1 and 2 μM) while increasing it at 10 μM PhE. Perplexingly, depolarization by 40 mM KCl-induced contraction of MA was commonly enhanced by the three fatty acids. The 40 mM KCl-contraction of DFA was also augmented by linoleic and oleic acids while not affected by palmitic acid. SFA persistently increased alpha-adrenergic contraction of systemic arteries whereas PUFA and MUFA attenuated PhE-induced contraction of skeletal arteries. PUFA and MUFA concentration-dependent dual effects on MA suggest differential mechanisms depending on the types of arteries. Further studies are needed to elucidate underlying mechanisms of the various effects of FFA on systemic arteries.
机译:游离脂肪酸(FFA)的摄入量可调节血压和血管反应性,但其对全身动脉收缩性的直接作用尚不清楚。我们研究了饱和脂肪酸(SFA,棕榈酸),多不饱和脂肪酸(PUFA,亚油酸)和单不饱和脂肪酸(MUFA,油酸)对肠系膜(MA)和股深动脉(DFA)收缩力的影响。 )的Sprague–Dawley大鼠。将分离的MA和DFA安装在双线肌电描记器上,在有或没有FFA的情况下,均可得到苯肾上腺素(PhE,1-10μM)浓度依赖性的收缩。与100μM棕榈酸一起孵育可显着增加PhE诱导的两条动脉收缩。在MA中,用100μM的亚油酸治疗可减少1μM的PhE诱导的收缩,同时增加对更高的PhE浓度的反应。在DFA中,亚油酸略微降低了PhE诱导的收缩,而200μM油酸则显着降低了收缩。在MA中,油酸在低PhE浓度(1和2μM)下会减少收缩,而在10μMPhE时会增加收缩。令人困惑的是,三种脂肪酸通常会增强40 mM KCl诱导的MA的去极化作用。亚油酸和油酸还增加了DFA的40 mM KCl收缩,而不受棕榈酸的影响。 SFA持续增加全身动脉的α-肾上腺素收缩,而PUFA和MUFA减弱PhE诱导的骨骼动脉收缩。 PUFA和MUFA对MA的浓度依赖性双重效应提示取决于动脉类型的不同机制。需要进一步的研究来阐明FFA对全身动脉的各种作用的潜在机制。

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