Department of Physiology, College of Medicine, University of Saskatchewan, Saskatoon, SK, Canada.
Diabetes Obes Metab. 2013 Nov;15(11):1029-39. doi: 10.1111/dom.12130. Epub 2013 Jun 30.
Visceral adiposity and impaired glucose metabolism are common patho-physiological features in patients co-morbid with obesity and type-2 diabetes. We investigated the effects of the heme-oxygenase (HO) inducer hemin and the HO blocker stannous-mesoporphyrin (SnMP) on glucose metabolism, adipocyte hypertrophy and pro-inflammatory cytokines/mediators in Zucker diabetic fatty (ZDF) rats, a model characterized by obesity and type-2 diabetes.
Histological, morphological/morphometrical, Western immunoblotting, enzyme immunoassay, ELISA and spectrophotometric analysis were used.
Treatment with hemin enhanced HO-1, HO activity and cGMP, but suppressed retroperitoneal adiposity and abated the elevated levels of macrophage-chemoattractant protein-1 (MCP-1), ICAM-1, tumour necrosis factor-alpha (TNF-α), interleukin 6 (IL-6), IL-1β, NF-κB, c-Jun-NH2-terminal-kinase (JNK) and activating-protein (AP-1), with parallel reduction of adipocyte hypertrophy. Correspondingly, important proteins of lipid metabolism and insulin-signalling such as lipoprotein lipase (LPL), insulin-receptor substrate-1 (IRS-1), GLUT4, PKB/Akt, adiponectin, the insulin-sensitizing and anti-inflammatory protein and adenosine-monophosphate-activated protein kinase (AMPK) were significantly enhanced in hemin-treated ZDF rats.
Elevated retroperitoneal adiposity and the high levels of MCP-1, ICAM-1, TNF-α, IL-6, IL-1β, NF-κB, JNK and AP-1 in untreated ZDF are patho-physiological factors that exacerbate inflammatory insults, aggravate adipocyte hypertrophy, with corresponding reduction of adiponectin and deregulation of insulin-signalling and lipid metabolism. Therefore, the suppression of MCP-1, ICAM-1, TNF-α, IL-6, IL-1β, NF-κB, JNK, AP-1 and adipocyte hypertrophy, with the associated enhancement of LPL, adiponectin, AMPK, IRS-1, GLUT4, PKB/Akt and cGMP in hemin-treated ZDF are among the multifaceted mechanisms by which the HO system combats inflammation to potentiate insulin signalling and improve glucose and lipid metabolism. Thus, HO inducers may be explored in the search of novel remedies against the co-morbidities of obesity, dysfunctional lipid metabolism and impaired glucose metabolism.
内脏肥胖和葡萄糖代谢受损是肥胖和 2 型糖尿病并存患者的常见病理生理特征。我们研究血红素加氧酶(HO)诱导剂血红素和 HO 阻断剂锡原卟啉(SnMP)对 Zucker 糖尿病肥胖(ZDF)大鼠葡萄糖代谢、脂肪细胞肥大和促炎细胞因子/介质的影响,ZDF 大鼠模型的特征是肥胖和 2 型糖尿病。
组织学、形态学/形态计量学、Western 免疫印迹、酶免疫分析、ELISA 和分光光度分析。
血红素处理增强了 HO-1、HO 活性和 cGMP,但抑制了腹膜后肥胖,并减轻了巨噬细胞趋化因子-1(MCP-1)、细胞间黏附分子-1(ICAM-1)、肿瘤坏死因子-α(TNF-α)、白细胞介素 6(IL-6)、白细胞介素 1β(IL-1β)、核因子-κB(NF-κB)、c-Jun-NH2-末端激酶(JNK)和激活蛋白(AP-1)的升高水平,同时脂肪细胞肥大减少。相应地,脂蛋白脂肪酶(LPL)、胰岛素受体底物-1(IRS-1)、GLUT4、蛋白激酶 B/Akt(PKB/Akt)、脂联素、胰岛素增敏和抗炎蛋白和腺苷一磷酸激活蛋白激酶(AMPK)等重要的脂质代谢和胰岛素信号蛋白显著增强。
未经处理的 ZDF 大鼠腹膜后脂肪组织增多,MCP-1、ICAM-1、TNF-α、IL-6、IL-1β、NF-κB、JNK 和 AP-1 水平升高,是加重炎症损伤、加重脂肪细胞肥大的病理生理因素,相应的脂联素减少,胰岛素信号和脂质代谢失调。因此,血红素处理抑制 MCP-1、ICAM-1、TNF-α、IL-6、IL-1β、NF-κB、JNK、AP-1 和脂肪细胞肥大,同时增强 ZDF 中的 LPL、脂联素、AMPK、IRS-1、GLUT4、PKB/Akt 和 cGMP,是 HO 系统对抗炎症以增强胰岛素信号和改善葡萄糖和脂质代谢的多种机制之一。因此,血红素诱导剂可能被探索用于寻找肥胖、脂质代谢功能障碍和葡萄糖代谢受损并存的新型治疗方法。