[Change of spinal neuronal nitric oxide synthase expression in rats with painful diabetic neuropathy].
Weicheng Zhao, Meijuan Liao, Wenxuan Zhang, Hanbing Wang, Hongzhen Liu, Chengxiang Yang, Bin Zhang
Abstract
Weicheng Zhao, Meijuan Liao, Wenxuan Zhang, Hanbing Wang, Hongzhen Liu, Chengxiang Yang, Bin Zhang
Abstract
OBJECTIVE: To observe the change of neuronal nitric oxide synthase (nNOS) expression in the spinal cord of diabetic rats with painful diabetic neuropathy. METHODS: Sixty SD rats were randomized equally into painful diabetic neuropathy group (DM group) and control group. Painful diabetic neuropathy was induced by intraperitoneal injection with STZ (60 mg/kg) in DM group, and the rats in the control group received a solvent injection. Blood glucose levels were measured before and at 2, 7, 14, 21, and 28 days after STZ injection (T1-6 respectively). Responses to the mechanical stimulus were measured with von Frey filament, and 50% paw withdraw threshold (PWT) and body weight were recorded at T1 and T3-6. At T1 and T3-6, 6 rats from each group were sacrificed to examine the expression of nNOS in the lumbar segments of the spinal cord using Western blotting. RESULTS: The level of blood glucose increased while the body weight decreased significantly after STZ injection in DM group (P<0.05). Comparing to those in the control group, PWT decreased while spinal nNOS expression increased significantly in DM group at T4-6 (P<0.05) showing an inverse correlation between them (P<0.01). CONCLUSION: The enhanced expression of spinal nNOS might be involved in the pathogenesis of painful diabetic neuropathy in rats.
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OBJECTIVE: To observe the change of neuronal nitric oxide synthase (nNOS) expression in the spinal cord of diabetic rats with painful diabetic neuropathy. METHODS: Sixty SD rats were randomized equally into painful diabetic neuropathy group (DM group) and control group. Painful diabetic neuropathy was induced by intraperitoneal injection with STZ (60 mg/kg) in DM group, and the rats in the control group received a solvent injection. Blood glucose levels were measured before and at 2, 7, 14, 21, and 28 days after STZ injection (T1-6 respectively). Responses to the mechanical stimulus were measured with von Frey filament, and 50% paw withdraw threshold (PWT) and body weight were recorded at T1 and T3-6. At T1 and T3-6, 6 rats from each group were sacrificed to examine the expression of nNOS in the lumbar segments of the spinal cord using Western blotting. RESULTS: The level of blood glucose increased while the body weight decreased significantly after STZ injection in DM group (P<0.05). Comparing to those in the control group, PWT decreased while spinal nNOS expression increased significantly in DM group at T4-6 (P<0.05) showing an inverse correlation between them (P<0.01). CONCLUSION: The enhanced expression of spinal nNOS might be involved in the pathogenesis of painful diabetic neuropathy in rats.
Key concepts: Diabetic neuropathy, Intraperitoneal injection, Nitric oxide synthase, Endocrinology, Medicine, Internal medicine, Spinal cord, Nitric oxide