Karimi Seyed Assad, Komaki Alireza, Salehi Iraj, Sarihi Abdolrahman, Shahidi Siamak
Neurophysiology Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.
Neurochem Res. 2015 Apr;40(4):811-7. doi: 10.1007/s11064-015-1531-3. Epub 2015 Feb 6.
In the hippocampus, metabotropic glutamate receptors (mGluRs) are involved in various forms of synaptic plasticity. High-fat diets (HFDs) adversely influence hippocampal structure and function and induce changes in hippocampal glutamate metabolism and neurotransmission. Here, we studied the induction of hippocampal long-term potentiation (LTP) while blocking group II mGluR2/3. Thirty-two male Wistar rats were assigned into four groups: a control group that consumed an ordinary diet; a HFD group that ate a HFD; "HFD plus LY341495" ate a HFD and later received a selective group II metabotropic glutamate receptor antagonist; and "Control plus LY341495" group. After 6 months on the specified diet, the rats were anesthetized with intraperitoneal injection of ketamine and xylazin, and placed in a stereotaxic apparatus for surgery, electrode implantation, and field potential recording. We microinjected LY341495 solution unilaterally into the dentate gyrus (DG) to block mGluR2/3. The population spike (PS) amplitude and slope of excitatory post synaptic potentials (EPSP) were measured in the DG area in response to stimulation applied to the perforant pathway (400 Hz tetanization). We found that, after tentanizing the perforant pathway to induce LTP, HFD decreased PS amplitude and slope of EPSP compared to controls. Moreover, blocking group II mGluRs increased LTP not only in controls, but also in rats fed on HFD. Therefore, our results show that LY341495 rescues hippocampal synaptic plasticity that can be impaired by a HFD. In summary, these results indicate that mGluR2/3 inhibition may have stimulatory effects on LTP induction in the DG.
在海马体中,代谢型谷氨酸受体(mGluRs)参与多种形式的突触可塑性。高脂饮食(HFDs)会对海马体的结构和功能产生不利影响,并诱导海马体谷氨酸代谢和神经传递的变化。在此,我们在阻断II组mGluR2/3的同时研究了海马体长时程增强(LTP)的诱导。32只雄性Wistar大鼠被分为四组:一组为食用普通饮食的对照组;一组为食用高脂饮食的HFD组;“HFD加LY341495”组食用高脂饮食,随后接受选择性II组代谢型谷氨酸受体拮抗剂;以及“对照组加LY341495”组。在指定饮食6个月后,大鼠通过腹腔注射氯胺酮和赛拉嗪进行麻醉,并置于立体定位仪中进行手术、电极植入和场电位记录。我们将LY341495溶液单侧微量注射到齿状回(DG)以阻断mGluR2/3。在对穿通通路施加刺激(400 Hz强直刺激)时,测量DG区域的群体峰电位(PS)幅度和兴奋性突触后电位(EPSP)的斜率。我们发现,在对穿通通路进行强直刺激以诱导LTP后,与对照组相比,高脂饮食降低了PS幅度和EPSP斜率。此外,阻断II组mGluRs不仅在对照组中增强了LTP,在食用高脂饮食的大鼠中也增强了LTP。因此,我们的结果表明,LY341495挽救了可能因高脂饮食而受损的海马体突触可塑性。总之,这些结果表明mGluR2/3抑制可能对DG中LTP的诱导具有刺激作用。