Moradi Mojtaba, Hassanshahi Jalal, Rahmani Mohammad Reza, Shamsizadeh Ali, Kaeidi Ayat
Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, I.R. Iran.
Department of Physiology and Pharmacology, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, I.R. Iran.
Res Pharm Sci. 2024 Oct 22;19(5):561-572. doi: 10.4103/RPS.RPS_140_23. eCollection 2024 Oct.
Neuropathy is one of the common complications of diabetes mellitus. This study aimed to determine the analgesic and antiapoptotic effects of the aqueous extract of L. (Ach) in rats with experimental painful diabetic neuropathy by behavioral and molecular procedures.
Thirty male Wistar rats were divided into 5 groups including control, diabetes + saline, and diabetes + Ach extract (doses of 150, 300, and 600 mg/kg/day for 3 weeks, orally). A tail-flick test was performed to assess the pain threshold in different groups. Western blotting test was used to evaluate the apoptotic (Bax, Bcl2, cleaved caspase-3, and cytochrome-c) and inflammatory (TNF-α and NF-kB) protein factors in the lumbar portion of the spinal cord tissue. Also, commercial assay kits were used to evaluate oxidative stress factors (MDA, GPx, and SOD enzyme activity) in the lumbar portion of the spinal cord tissue.
FINDINGS/RESULTS: Results showed that administering Ach extract at the doses of 300 and 600 mg/kg/day significantly increased the nociception threshold in treated diabetic animals compared to untreated diabetic animals. Moreover, the treatment of diabetic animals with Ach extract (300 and 600 mg/kg/day) significantly reduced the oxidative stress, inflammation, and apoptosis biochemical indicators in the lumbar spinal cord tissue compared to the untreated diabetic group.
The findings showed that Ach extract has neuroprotective and anti-nociceptive effects in rats with diabetic neuropathy. The effects can be due to the inhibition of oxidative stress, inflammation, and apoptosis in the spinal cord tissue.
神经病变是糖尿病常见的并发症之一。本研究旨在通过行为学和分子学方法,确定L. (Ach)水提取物对实验性疼痛性糖尿病神经病变大鼠的镇痛和抗凋亡作用。
将30只雄性Wistar大鼠分为5组,包括对照组、糖尿病+生理盐水组,以及糖尿病+Ach提取物组(剂量分别为150、300和600 mg/kg/天,口服,持续3周)。进行甩尾试验以评估不同组的疼痛阈值。采用蛋白质免疫印迹法检测脊髓组织腰段中凋亡相关蛋白因子(Bax、Bcl2、裂解的caspase-3和细胞色素c)及炎症相关蛋白因子(TNF-α和NF-κB)。此外,使用商业检测试剂盒评估脊髓组织腰段中的氧化应激因子(丙二醛、谷胱甘肽过氧化物酶和超氧化物歧化酶活性)。
结果显示,与未治疗的糖尿病动物相比,以300和600 mg/kg/天的剂量给予Ach提取物可显著提高治疗组糖尿病动物的痛觉阈值。此外,与未治疗的糖尿病组相比,用Ach提取物(300和600 mg/kg/天)治疗糖尿病动物可显著降低脊髓组织腰段中的氧化应激、炎症和凋亡生化指标。
研究结果表明,Ach提取物对糖尿病神经病变大鼠具有神经保护和抗伤害感受作用。这些作用可能是由于其抑制了脊髓组织中的氧化应激、炎症和凋亡。