Molecular Neurobiology and Cell Biology Unit, Centre for Neuroscience, Department of Biotechnology, Cochin University of Science and Technology, Cochin- 682 022, Kerala, India.
J Biomed Sci. 2010 Sep 25;17(1):78. doi: 10.1186/1423-0127-17-78.
Diabetes and stress stimulate hippocampal 5-HT synthesis, metabolism and release. The present study was carried out to find the effects of insulin, Aegle marmelose alone and in combination with pyridoxine on the hippocampal 5-HT, 5-HT(2A) receptor subtype, gene expression studies on 5-HT(2A), 5-HTT, INSR, immunohistochemical studies and elevated plus maze in streptozotocin induced diabetic rats. 5-HT content showed a significant decrease (p < 0.001) and a significant increase (p < 0.001) in 5-HIAA in hippocampus of diabetic rats compared to control. 5-HT receptor binding parameters B(max) and Kd showed a significant decrease (p < 0.001) whereas 5-HT(2A) receptor binding parameters Bmax showed a significant decrease (p < 0.001) with a significant increase (p < 0.05) in Kd in hippocampus of diabetic rats compared to control. Gene expression studies of 5-HT(2A), 5-HTT and INSR in hippocampus showed a significant down regulation (p < 0.001) in diabetic rats compared to control. Pyridoxine treated in combination with insulin and A. marmelose to diabetic rats reversed the 5-HT content, B(max), Kd of 5-HT, 5-HT(2A) and gene expression of 5-HT(2A), 5-HTT and INSR in hippocampus to near control. The gene expression of 5-HT(2A) and 5-HTT were confirmed by immunohistochemical studies. Behavioural studies using elevated plus maze showed that serotonin through its transporter significantly increased (p < 0.001) anxiety-related traits in diabetic rats which were corrected by combination therapy. Our results suggest that pyridoxine treated in combination with insulin and A. marmelose has a role in the regulation of insulin synthesis and release, normalising diabetic related stress and anxiety through hippocampal serotonergic function. This has clinical significance in the management of diabetes.
糖尿病和压力会刺激海马体 5-HT 的合成、代谢和释放。本研究旨在探讨胰岛素、酸橙单独及与吡哆醇联合应用对糖尿病大鼠海马体 5-HT、5-HT(2A)受体亚型、5-HT(2A)、5-HTT、INSR 基因表达、5-HT 免疫组织化学研究和高架十字迷宫的影响。与对照组相比,糖尿病大鼠海马体 5-HT 含量显著降低(p<0.001),5-HIAA 含量显著升高(p<0.001)。5-HT 受体结合参数 Bmax 和 Kd 显著降低(p<0.001),而 5-HT(2A)受体结合参数 Bmax 显著降低(p<0.001),Kd 显著升高(p<0.05)。与对照组相比,糖尿病大鼠海马体 5-HT(2A)、5-HTT 和 INSR 基因表达均显著下调(p<0.001)。与糖尿病大鼠相比,吡哆醇联合胰岛素和酸橙治疗可逆转 5-HT 含量、Bmax、Kd 的变化,以及海马体 5-HT、5-HT(2A)和基因表达的变化。5-HT(2A)和 5-HTT 的基因表达通过免疫组织化学研究得到了证实。高架十字迷宫行为学研究表明,5-HT 通过其转运体显著增加(p<0.001)糖尿病大鼠的焦虑相关特征,联合治疗可纠正这一特征。我们的结果表明,吡哆醇联合胰岛素和酸橙治疗在调节胰岛素合成和释放方面发挥作用,通过海马体 5-羟色胺能功能使糖尿病相关应激和焦虑正常化。这在糖尿病的治疗中具有临床意义。