Maegawa H, Katsube N, Okegawa T, Aishita H, Kawasaki A
Preclinical Research Department, Ono Pharmaceutical Co., Ltd., Osaka, Japan.
Life Sci. 1992;51(4):285-93. doi: 10.1016/0024-3205(92)90087-6.
We examined the effects of arginine-vasopressin (AVP) C-terminal fragment 4-9, which facilitates learning and memory, on the extracellular acetylcholine (ACh) release in hippocampus of freely-moving rats using the microdialysis technique. Following administration of AVP4-9, p-Glu-Asn-Cys[Cys]-Pro-Arg-Gly-NH2, through the dialysis probe into the hippocampus, ACh levels in dialysates from the hippocampus increased markedly in dose and time dependent manner at 2-2.5 and 2.5-3 hr. AVP1-9, the parent peptide, has a similar enhancing effect on ACh release as AVP4-9. Stimulated ACh release by AVP4-9 was significantly inhibited by V1-selective receptor antagonist ([1-(beta-mercapto-beta,beta-cyclopentamethylenepropionic acid), 2-(O-methyl)-tyrosine]AVP), but not by V2-selective antagonist ([1-(beta-mercapto-beta,beta-cyclopentamethylenepropionic acid), 2-D-Ile, 4-Ile]AVP). From these observations, it is demonstrated that AVP4-9 stimulates the ACh release in rat hippocampus via mediating V1-like vasopressin receptors.
我们使用微透析技术,研究了促进学习和记忆的精氨酸加压素(AVP)C末端片段4-9对自由活动大鼠海马细胞外乙酰胆碱(ACh)释放的影响。通过透析探针将AVP4-9(p-Glu-Asn-Cys[Cys]-Pro-Arg-Gly-NH2)注入海马后,在2至2.5小时和2.5至3小时时,海马透析液中的ACh水平呈剂量和时间依赖性显著增加。母体肽AVP1-9对ACh释放具有与AVP4-9相似的增强作用。AVP4-9刺激的ACh释放被V1选择性受体拮抗剂([1-(β-巯基-β,β-环戊亚甲基丙酸), 2-(O-甲基)-酪氨酸]AVP)显著抑制,但未被V2选择性拮抗剂([1-(β-巯基-β,β-环戊亚甲基丙酸), 2-D-异亮氨酸, 4-异亮氨酸]AVP)抑制。从这些观察结果表明,AVP4-9通过介导类V1血管加压素受体刺激大鼠海马中的ACh释放。