首页> 外文期刊>Clinical and experimental pharmacology & physiology >Effect of indole-3-carbinol on ethanol-induced liver injury and acetaldehyde-stimulated hepatic stellate cells activation using precision-cut rat liver slices.
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Effect of indole-3-carbinol on ethanol-induced liver injury and acetaldehyde-stimulated hepatic stellate cells activation using precision-cut rat liver slices.

机译:吲哚-3-甲醇对乙醇诱导的肝损伤和乙醛刺激的肝星状细胞活化的影响,采用精密切割的大鼠肝切片。

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摘要

1. Indole-3-carbinol (I3C), a major indole compound found in high levels in cruciferous vegetables, shows a broad spectrum of biological activities. However, few studies have reported the effect of I3C on alcoholic liver injury. In the present study, we investigated the protective effect of I3C on acute ethanol-induced hepatotoxicity and acetaldehyde-stimulated hepatic stellate cells (HSC) activation using precision-cut liver slices (PCLS). 2. Rat PCLS were incubated with 50 mmol/L ethanol or 350 mumol/L acetaldehyde, and different concentrations (100-400 mumol/L) of I3C were added into the culture system of these two liver injury models, respectively. Hepatotoxicity was assessed by measuring enzyme leakage and malondialdehyde (MDA) content in tissue. Activities of alcoholic enzymes were also determined. alpha-Smooth muscle actin (alpha-SMA), transforming growth factor (TGF-beta(1) ) and hydroxyproline (HYP) were used as indices to evaluate the activation of HSC. In addition, matrix metalloproteinase-1 (MMP-1) and the tissue inhibitor of metalloproteinase (TIMP-1) were observed to estimate collagen degradation. 3. I3C significantly reduced the enzyme leakage in ethanol-treated slices. In I3C groups, cytochrome P450 (CYP) 2E1 activities were inhibited by 40.9-51.8%, whereas alcohol dehydrogenase (ADH) activity was enhanced 1.6-fold compared with the ethanol-treated group. I3C also showed an inhibitory effect against HSC activation and collagen production stimulated by acetaldehyde. After being incubated with I3C (400 mumol/L), the expression of MMP-1 was markedly enhanced, whereas TIMP-1 was decreased. 4. These results showed that I3C protected PCLS against alcoholic liver injury, which might be associated with the regulation of ethanol metabolic enzymes, attenuation of oxidative injury and acceleration of collagen degradation.
机译:1.吲哚-3-甲醇(I3C)是十字花科蔬菜中含量高的主要吲哚化合物,具有广泛的生物活性。但是,很少有研究报道I3C对酒精性肝损伤的影响。在本研究中,我们研究了I3C对急性乙醇诱导的肝毒性和乙醛刺激的肝星状细胞(HSC)活化的精确切割肝片(PCLS)的保护作用。 2.将大鼠PCLS与50 mmol / L乙醇或350μmol/ L乙醛孵育,并将不同浓度(100-400μmol/ L)的I3C分别加入这两种肝损伤模型的培养系统中。通过测量组织中的酶渗漏和丙二醛(MDA)含量来评估肝毒性。还测定了酒精酶的活性。 α-平滑肌肌动蛋白(alpha-SMA),转化生长因子(TGF-beta(1))和羟脯氨酸(HYP)被用作评估HSC活化的指标。此外,观察到基质金属蛋白酶-1(MMP-1)和金属蛋白酶组织抑制剂(TIMP-1)估计胶原蛋白降解。 3. I3C显着减少了乙醇处理过的切片中的酶泄漏。在I3C组中,细胞色素P450(CYP)2E1活性被抑制了40.9-51.8%,而与乙醇处理组相比,乙醇脱氢酶(ADH)活性提高了1.6倍。 I3C还显示出对乙醛刺激的HSC活化和胶原蛋白产生的抑制作用。与I3C(400μmol/ L)孵育后,MMP-1的表达显着增强,而TIMP-1则降低。 4.这些结果表明,I3C保护PCLS免于酒精性肝损伤,这可能与乙醇代谢酶的调节,氧化损伤的减弱和胶原蛋白降解的加速有关。

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