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外源性化学物质介导的糖尿病发生机制:二氯松或莠去津在发育阶段的暴露会导致果蝇发生 1 型或 2 型糖尿病。

Xenobiotic mediated diabetogenesis: Developmental exposure to dichlorvos or atrazine leads to type 1 or type 2 diabetes in Drosophila.

机构信息

Embryotoxicology Laboratory, Environmental Toxicology Group, CSIR-Indian Institute of Toxicology Research (CSIR-IITR), Vishvigyan Bhavan, 31, Mahatma Gandhi Marg, Lucknow, 226 001, Uttar Pradesh, India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201 002, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201 002, India; Analytical Chemistry Laboratory, Regulatory Toxicology Group, CSIR-Indian Institute of Toxicology Research, Lucknow, 226001, Uttar Pradesh, India.

出版信息

Free Radic Biol Med. 2019 Sep;141:461-474. doi: 10.1016/j.freeradbiomed.2019.07.013. Epub 2019 Jul 15.

Abstract

The increased incidence of diabetes to the magnitude of a global epidemic is attributed to non-traditional risk factors, including exposure to environmental chemicals. However, the contribution of xenobiotic exposure during the development of an organism to the etiology of diabetes is not fully addressed. Developing stages are more susceptible to chemical insult, but knowledge on the consequence of the same to the onset of diabetes is residual. In this context, by using Drosophila melanogaster having conserved Insulin/Insulin growth factor-like signaling (IIS) as well as glucose homeostasis as a model, we evaluated the potential of developmental exposure to dichlorvos (DDVP, an organophosphorus pesticide) or atrazine (herbicide) to cause diabetes in exposed organisms. Flies exposed to DDVP during their development display insulin deficiency or type 1 diabetes (T1D) while those exposed to atrazine show insulin resistance or type 2 diabetes (T2D), suggesting that exposure to these xenobiotics during organismal development can result in diabetes and that different mechanisms underlie pesticide mediated diabetes. We show that oxidative stress-mediated c-Jun N-terminal kinase (JNK) signaling activation underlies insulin resistance in flies exposed to atrazine during their development while DDVP-mediated T1D involves activation of caspase-mediated cell death pathway. Mitigation of oxidative stress through over-expression of SOD2 in atrazine (20μg/ml) exposed flies, revealed significantly decreased oxidative stress levels and reduced phosphorylation of JNK. Moreover, glucose and Akt phosphorylation levels in SOD2 over-expression flies exposed to atrazine were comparable to those in controls, suggesting restoration in insulin sensitivity. Therefore, exposure to xenobiotics during development is a common risk factor for the development of type 1 or type 2 diabetes. Accordingly, the present study cautions against the use of such diabetogenic pesticides. Also, mitigation of oxidative stress or anti-oxidant supplementation could be a potential therapy for xenobiotic mediated type 2 diabetes.

摘要

糖尿病发病率的增加达到了全球流行的程度,这归因于非传统的危险因素,包括接触环境化学物质。然而,在生物体发育过程中暴露于外源性化学物质对糖尿病病因的贡献尚未得到充分解决。发育阶段更容易受到化学物质的侵袭,但对于相同物质对糖尿病发病的影响的了解仍有限。在这种情况下,我们使用具有保守的胰岛素/胰岛素样生长因子样信号(IIS)以及葡萄糖稳态的黑腹果蝇作为模型,评估了在发育过程中暴露于二氯膦(DDVP,一种有机磷农药)或莠去津(除草剂)对暴露生物体引起糖尿病的潜力。在发育过程中暴露于 DDVP 的果蝇表现出胰岛素缺乏或 1 型糖尿病(T1D),而暴露于莠去津的果蝇则表现出胰岛素抵抗或 2 型糖尿病(T2D),这表明在生物体发育过程中暴露于这些外源性化学物质会导致糖尿病,并且不同的机制是农药介导的糖尿病的基础。我们表明,在发育过程中暴露于莠去津的果蝇中,氧化应激介导的 c-Jun N-末端激酶(JNK)信号通路的激活是胰岛素抵抗的基础,而 DDVP 介导的 T1D 涉及半胱天冬酶介导的细胞死亡途径的激活。通过在莠去津(20μg/ml)暴露的果蝇中过表达 SOD2 来减轻氧化应激,发现氧化应激水平显著降低,JNK 的磷酸化减少。此外,在暴露于莠去津的 SOD2 过表达果蝇中,葡萄糖和 Akt 的磷酸化水平与对照相比相似,表明胰岛素敏感性得到恢复。因此,在发育过程中暴露于外源性化学物质是 1 型或 2 型糖尿病发展的共同危险因素。因此,本研究警告不要使用此类致糖尿病的农药。此外,减轻氧化应激或抗氧化剂补充可能是外源性化学物质介导的 2 型糖尿病的潜在治疗方法。

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