Zhao Wei-Cheng, Zhang Bin, Liao Mei-Juan, Zhang Wen-Xuan, He Wan-You, Wang Han-Bing, Yang Cheng-Xiang
Department of Anesthesiology, The First People's Hospital of Foshan, 81# North of Rinlan Road, Foshan 528000, China.
Department of Anesthesiology, The First People's Hospital of Foshan, 81# North of Rinlan Road, Foshan 528000, China.
Neurosci Lett. 2014 Feb 7;560:81-5. doi: 10.1016/j.neulet.2013.12.019. Epub 2013 Dec 24.
Nicotinamide adenine dinucleotide phosphate (NADPH) oxidases are the main enzymes that produce oxidative stress, which plays an important role in painful diabetic neuropathy. Curcumin has been reported to exert an antinociceptive effect in a rat model of diabetic neuropathy by suppressing oxidative stress in the spinal cord. However, it remains unknown whether the mechanism by which curcumin ameliorates diabetic neuropathy can be attributed to spinal NADPH oxidases. This study was designed to determine the effect of curcumin on diabetic neuropathy and to investigate its precise mechanism in relation to NADPH oxidase-mediating oxidative stress in the spinal cord. Diabetic neuropathy was induced in Sprague-Dawley rats by intraperitoneal injection with 1% streptozotocin (STZ; 60 mg/kg). After the onset of diabetic neuropathy, a subset of the diabetic rats received daily intragastric administrations of curcumin (200mg/kg) or intraperitoneal injections of apocynin (2.5mg/kg) for 14 consecutive days, whereas other diabetic rats received equivalent volumes of normal saline (NS). STZ resulted in diabetic neuropathy with hyperglycemia and a lower paw withdrawal threshold (PWT), accompanied by elevations in the expression of the NADPH oxidase subunits p47(phox) and gp91(phox) and in the levels of hydrogen peroxide (H2O2) and malondialdehyde (MDA) and a reduction in superoxide dismutase (SOD) activity (P<0.05) in the spinal cord. Both curcumin and apocynin ameliorated diabetic neuropathy. In conclusion, curcumin attenuated neuropathic pain in diabetic rats, at least partly by inhibiting NADPH oxidase-mediating oxidative stress in the spinal cord.
烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶是产生氧化应激的主要酶类,氧化应激在糖尿病性周围神经病变中起重要作用。据报道,姜黄素通过抑制脊髓中的氧化应激,在糖尿病性周围神经病变大鼠模型中发挥镇痛作用。然而,姜黄素改善糖尿病性周围神经病变的机制是否可归因于脊髓中的NADPH氧化酶仍不清楚。本研究旨在确定姜黄素对糖尿病性周围神经病变的影响,并研究其与NADPH氧化酶介导的脊髓氧化应激相关的精确机制。通过腹腔注射1%链脲佐菌素(STZ;60mg/kg)诱导Sprague-Dawley大鼠发生糖尿病性周围神经病变。糖尿病性周围神经病变发病后,一部分糖尿病大鼠连续14天每天接受姜黄素(200mg/kg)灌胃或阿朴吗啡(2.5mg/kg)腹腔注射,而其他糖尿病大鼠接受等量的生理盐水(NS)。STZ导致糖尿病性周围神经病变伴高血糖和较低的爪部撤离阈值(PWT),同时脊髓中NADPH氧化酶亚基p47(phox)和gp91(phox)的表达升高,过氧化氢(H2O2)和丙二醛(MDA)水平升高,超氧化物歧化酶(SOD)活性降低(P<0.05)。姜黄素和阿朴吗啡均改善了糖尿病性周围神经病变。总之,姜黄素减轻了糖尿病大鼠的神经病理性疼痛,至少部分是通过抑制脊髓中NADPH氧化酶介导的氧化应激实现的。