Department of Physiology, Faculty of Medicine, Erciyes University, 38039 Kayseri, Turkey.
Neuropeptides. 2011 Feb;45(1):77-81. doi: 10.1016/j.npep.2010.11.004. Epub 2010 Dec 15.
Carnosine is a dipeptide synthesized by the carnosine synthetase from β-alanine and l-histidine. The well-known effects of carnosine may be related with mechanisms producing long-term potentiation which is one of the electrophysiological signs of memory. In the present study we aimed to investigate the effect of four different doses of carnosine on long-term potentiation in urethane-anesthetized rat. A bipolar stimulating electrode was placed in the medial perforant path and a double-barrel glass micropipette was placed in the dentate gyrus as the recording electrode. Artificial cerebrospinal fluid (in the control group) or carnosine (0.1, 1, 10, and 100μg/μL) was infused into the dentate gyrus. Our results showed that the I/O curve of the excitatory postsynaptic potential slope or population spike amplitude was not significantly shifted by carnosine. We found that population spike amplitude increased to 244% and 287% at the dose of 100μg/μL in the post-tetanic and induction phases, respectively, but decreased to 163% and 186% at the dose of 0.1μg/μL and to 145% and 162% at the dose of 1μg/μL when compared with 203% and 232% of the control values. However, there were no significant differences for the slope of excitatory postsynaptic potential. Carnosine had no effect on the EPSP slope or PS amplitude recorded from the dentate gyrus in response to test stimuli when high-frequency stimulation was not delivered. In the present study, we speculated that the effects of carnosine in lower or higher doses could be explained by its effect on different processes, such as soluble guanylyl cyclase inhibition or the conversion of carnosine into histamine.
肌肽是一种二肽,由β-丙氨酸和 l-组氨酸通过肌肽合成酶合成。肌肽的许多众所周知的作用可能与产生长时程增强的机制有关,长时程增强是记忆的一种电生理标志。在本研究中,我们旨在研究四种不同剂量的肌肽对乌拉坦麻醉大鼠长时程增强的影响。双极刺激电极置于内侧穿通路径,双管玻璃微电极置于齿状回作为记录电极。人工脑脊液(在对照组)或肌肽(0.1、1、10 和 100μg/μL)被注入齿状回。我们的结果表明,肌肽并没有显著改变兴奋性突触后电位斜率或群体锋电位幅度的 I/O 曲线。我们发现,在强直后和诱导期,群体锋电位幅度分别增加到 100μg/μL 剂量的 244%和 287%,但在 0.1μg/μL 剂量下降至 163%和 186%,在 1μg/μL 剂量下降至 145%和 162%,与对照值的 203%和 232%相比。然而,兴奋性突触后电位斜率没有显著差异。当未进行高频刺激时,肌肽对齿状回记录的测试刺激的 EPSP 斜率或 PS 幅度没有影响。在本研究中,我们推测,较低或较高剂量的肌肽的作用可以通过其对不同过程的影响来解释,例如可溶性鸟苷酸环化酶抑制或肌肽转化为组胺。