Spruijt B M
Institute of Molecular Biology, University of Utrecht, The Netherlands.
Psychoneuroendocrinology. 1992 Aug;17(4):315-25. doi: 10.1016/0306-4530(92)90037-8.
ACTH-like neuropeptides have been investigated in various paradigms such as cognition, neuronal damage and neuronal excitation. All their effects may be collectively described as modulation of neural plasticity. However, the mechanism of action accounting for these effects remains to be demonstrated. This report is an overview of the data and has incorporated some additional findings of the influence of the ACTH4-9 analog, Org2766, on neuronal excitation, especially in the hippocampus. An interaction with NMDA receptors may account for the various aspects of plasticity. Based on recent findings demonstrating that the ACTH4-9 analog counteracts both the NMDA antagonist, AP5, and NMDA-induced explosive running behavior, the hypothesis is put forward that glutamatergic neurotransmission is involved in behavioral changes induced by the ACTH4-9 analog.
促肾上腺皮质激素(ACTH)样神经肽已在多种范例中进行了研究,如认知、神经元损伤和神经元兴奋。它们所有的作用都可统称为对神经可塑性的调节。然而,解释这些作用的作用机制仍有待证实。本报告是对相关数据的概述,并纳入了一些关于ACTH4-9类似物Org2766对神经元兴奋影响的额外发现,特别是在海马体中的影响。与N-甲基-D-天冬氨酸(NMDA)受体的相互作用可能解释可塑性的各个方面。基于最近的研究结果表明ACTH4-9类似物可抵消NMDA拮抗剂AP5以及NMDA诱导的爆发性奔跑行为,因此提出谷氨酸能神经传递参与了ACTH4-9类似物诱导的行为变化这一假说。