Leng Yi-Ping, Qiu Ni, Fang Wei-jin, Zhang Mei, He Zhi-Min, Xiong Yan
Department of Pharmacology, School of Pharmaceutical Sciences, Central South University, Changsha, Hunan, P.R. China.
Department of Pharmacology, Guangzhou Research Institute of Snake Venom and School of Pharmaceutical Sciences, Guangzhou Medical University, Guangzhou, Guangdong, P.R. China.
PLoS One. 2014 Jun 11;9(2):e97125. doi: 10.1371/journal.pone.0097125. eCollection 2014.
Increasing evidence suggested that endoplasmic reticulum (ER) stress contributes to insulin resistance, which plays an important role in the development of type 2 diabetes mellitus (T2DM). Accumulation of endogenous nitric oxide synthase (NOS) inhibitor, asymmetric dimethylarginine (ADMA), is associated with insulin resistance, T2DM, and diabetic cardiovascular complications, although the mechanisms have not been elucidated. This study was to determine whether elevated endogenous ADMA is involved in hepatic ER stress of type 2 diabetic rats, verify their causal relationship, and elucidate the potential mechanism underlying ADMA induced ER stress in rat hepatocytes.
Immunoglobulin binding protein (Bip) transcription, eukaryotic initiation factor 2α kinase (eIF2α) phosphorylation, X box-binding protein-1 (XBP-1) mRNA splicing and C/EBP homologues protein (CHOP) expression were measured to reflect ER stress. Contents of ADMA and nitrite/nitrate as well as activities or expression of NOS and dimethylarginine dimethylaminohydrolase (DDAH) were detected to show the changes in DDAH/ADMA/NOS/NO pathway. The lipid peroxidation product malondialdehyde content and antioxidant enzyme superoxide dismutase activity were analyzed to evaluate oxidative stress.
ER stress was provoked in the liver of type 2 diabetic rats, as expressed by increases of Bip transcription, eIF2α phosphorylation, XBP-1 splicing and CHOP expression, all of which were in parallel with the elevation of serum ADMA, suppression of NO generation, NOS and DDAH activities in the liver. Exposure of hepatocytes to ADMA or hydrogen peroxide also induced ER stress, which was associated with the inhibition of NO production and increase of oxidative stress. Treatment of hepatocytes with antioxidant pyrrolidine dithiocarbamate not only decreased ADMA-induced oxidative stress and inhibition of NO production but also reduced ADMA-triggered ER stress.
These results indicate that increased endogenous ADMA contributes to hepatic ER stress in type 2 diabetic rats, and the mechanism underlying ADMA-induced ER stress may relate to oxidative stress via NOS uncoupling.
越来越多的证据表明内质网(ER)应激促成胰岛素抵抗,而胰岛素抵抗在2型糖尿病(T2DM)的发生发展中起重要作用。内源性一氧化氮合酶(NOS)抑制剂非对称二甲基精氨酸(ADMA)的蓄积与胰岛素抵抗、T2DM及糖尿病心血管并发症相关,尽管其机制尚未阐明。本研究旨在确定内源性ADMA升高是否参与2型糖尿病大鼠的肝脏内质网应激,验证它们之间的因果关系,并阐明ADMA诱导大鼠肝细胞内质网应激的潜在机制。
检测免疫球蛋白结合蛋白(Bip)转录、真核起始因子2α激酶(eIF2α)磷酸化、X盒结合蛋白1(XBP-1)mRNA剪接及C/EBP同源蛋白(CHOP)表达以反映内质网应激。检测ADMA和亚硝酸盐/硝酸盐含量以及NOS和二甲基精氨酸二甲胺水解酶(DDAH)的活性或表达,以显示DDAH/ADMA/NOS/NO途径的变化。分析脂质过氧化产物丙二醛含量和抗氧化酶超氧化物歧化酶活性以评估氧化应激。
2型糖尿病大鼠肝脏中内质网应激被激发,表现为Bip转录增加、eIF2α磷酸化增加、XBP-1剪接增加及CHOP表达增加,所有这些均与血清ADMA升高、肝脏中NO生成受抑制、NOS和DDAH活性降低平行。肝细胞暴露于ADMA或过氧化氢也诱导内质网应激,这与NO生成受抑制及氧化应激增加相关。用抗氧化剂吡咯烷二硫代氨基甲酸盐处理肝细胞不仅降低了ADMA诱导的氧化应激和对NO生成的抑制,还减轻了ADMA引发的内质网应激。
这些结果表明,内源性ADMA增加促成2型糖尿病大鼠的肝脏内质网应激,且ADMA诱导内质网应激的机制可能与通过NOS解偶联导致的氧化应激有关。