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油酸以及富含油酸的花生油在体外和体内系统中均可逆转炎性细胞因子肿瘤坏死因子-α对胰岛素生成的抑制作用。

Oleic acid and peanut oil high in oleic acid reverse the inhibitory effect of insulin production of the inflammatory cytokine TNF-alpha both in vitro and in vivo systems.

作者信息

Vassiliou Evros K, Gonzalez Andres, Garcia Carlos, Tadros James H, Chakraborty Goutam, Toney Jeffrey H

机构信息

Department of Biological Sciences, Kean University, 1000 Morris Avenue, Union, New Jersey 07083, USA.

出版信息

Lipids Health Dis. 2009 Jun 26;8:25. doi: 10.1186/1476-511X-8-25.

Abstract

BACKGROUND

Chronic inflammation is a key player in pathogenesis. The inflammatory cytokine, tumor necrosis factor-alpha is a well known inflammatory protein, and has been a therapeutic target for the treatment of diseases such as Rheumatoid Arthritis and Crohn's Disease. Obesity is a well known risk factor for developing non-insulin dependent diabetes melitus. Adipose tissue has been shown to produce tumor necrosis factor-alpha, which has the ability to reduce insulin secretion and induce insulin resistance. Based on these observations, we sought to investigate the impact of unsaturated fatty acids such as oleic acid in the presence of TNF-alpha in terms of insulin production, the molecular mechanisms involved and the in vivo effect of a diet high in oleic acid on a mouse model of type II diabetes, KKAy.

METHODS

The rat pancreatic beta cell line INS-1 was used as a cell biological model since it exhibits glucose dependent insulin secretion. Insulin production assessment was carried out using enzyme linked immunosorbent assay and cAMP quantification with competitive ELISA. Viability of TNF-alpha and oleic acid treated cells was evaluated using flow cytometry. PPAR-gamma translocation was assessed using a PPRE based ELISA system. In vivo studies were carried out on adult male KKAy mice and glucose levels were measured with a glucometer.

RESULTS

Oleic acid and peanut oil high in oleic acid were able to enhance insulin production in INS-1. TNF-alpha inhibited insulin production but pre-treatment with oleic acid reversed this inhibitory effect. The viability status of INS-1 cells treated with TNF-alpha and oleic acid was not affected. Translocation of the peroxisome proliferator- activated receptor transcription factor to the nucleus was elevated in oleic acid treated cells. Finally, type II diabetic mice that were administered a high oleic acid diet derived from peanut oil, had decreased glucose levels compared to animals administered a high fat diet with no oleic acid.

CONCLUSION

Oleic acid was found to be effective in reversing the inhibitory effect in insulin production of the inflammatory cytokine TNF-alpha. This finding is consistent with the reported therapeutic characteristics of other monounsaturated and polyunsaturated fatty acids. Furthermore, a diet high in oleic acid, which can be easily achieved through consumption of peanuts and olive oil, can have a beneficial effect in type II diabetes and ultimately reverse the negative effects of inflammatory cytokines observed in obesity and non insulin dependent diabetes mellitus.

摘要

背景

慢性炎症是发病机制中的关键因素。炎性细胞因子肿瘤坏死因子-α是一种著名的炎性蛋白,一直是类风湿性关节炎和克罗恩病等疾病治疗的靶点。肥胖是发生非胰岛素依赖型糖尿病的一个众所周知的危险因素。脂肪组织已被证明能产生肿瘤坏死因子-α,它有能力减少胰岛素分泌并诱导胰岛素抵抗。基于这些观察结果,我们试图研究在肿瘤坏死因子-α存在的情况下,油酸等不饱和脂肪酸对胰岛素产生的影响、涉及的分子机制以及富含油酸的饮食对II型糖尿病小鼠模型KKAy的体内作用。

方法

大鼠胰腺β细胞系INS-1被用作细胞生物学模型,因为它表现出葡萄糖依赖性胰岛素分泌。使用酶联免疫吸附测定法进行胰岛素产生评估,并通过竞争性酶联免疫吸附测定法进行环磷酸腺苷定量。使用流式细胞术评估肿瘤坏死因子-α和油酸处理细胞的活力。使用基于过氧化物酶体增殖物激活受体应答元件的酶联免疫吸附测定系统评估过氧化物酶体增殖物激活受体γ的易位。对成年雄性KKAy小鼠进行体内研究,并用血糖仪测量血糖水平。

结果

油酸和富含油酸的花生油能够增强INS-1细胞中的胰岛素产生。肿瘤坏死因子-α抑制胰岛素产生,但用油酸预处理可逆转这种抑制作用。用肿瘤坏死因子-α和油酸处理的INS-1细胞的活力状态未受影响。在油酸处理的细胞中,过氧化物酶体增殖物激活受体转录因子向细胞核的易位增加。最后,与给予不含油酸的高脂肪饮食的动物相比,给予源自花生油的高油酸饮食的II型糖尿病小鼠的血糖水平降低。

结论

发现油酸可有效逆转炎性细胞因子肿瘤坏死因子-α对胰岛素产生的抑制作用。这一发现与其他单不饱和和多不饱和脂肪酸报道的治疗特性一致。此外,通过食用花生和橄榄油可以轻松实现的富含油酸的饮食,对II型糖尿病可能有有益作用,并最终逆转在肥胖症和非胰岛素依赖型糖尿病中观察到的炎性细胞因子的负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ce2/2706835/b944da8cb8bd/1476-511X-8-25-1.jpg

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