摘要
目的:研究柳珊瑚酸(Sub)、N柳珊瑚酰胺NN二环己基脲(SubDU),N环己基柳珊瑚酰胺(NCS)在影响记忆与抗胆碱酯酶(AChE)作用间的关系.方法:在被动回避操作装置上测定小鼠ipSub或其衍生物后的跳台潜伏期(SDL)和逃避潜伏期(EL);比色法测定AChE活力.结果:Sub19,SubDU30和Phys015mg·kg-1分别使成年小鼠的SDL延长195%,271%和210%,EL缩短56%,61%和33%;前二者尚同时使小鼠全脑匀浆AChE活力各降低17%和19%.大于上述剂量时,Sub和SubDU对SDL和EL的作用依剂量地减弱.Sub19,SubDU20和Phys015mg·kg-1还可使老年小鼠的SDL各延长187%,209%和152%,EL各缩短52%,62%和57%.三药尚明显改善由环己酰亚胺或东莨菪碱产生的记忆保持损害.NCS无上述作用.结论:Sub和SubDU对记忆的改善作用与其抗AChE有关.
AIM: To study the relationship between
the effects of suberogorgin (Sub) and its derivates on memory and
their anti acetylcholinesterase (AChE) actions. METHODS: The step
down latency (SDL) and the escape latency (EL) of mice were
determined at the same time in a passive avoidance task after Sub,
N subero ̄gorgamide N N dicyclohexyl urea (Sub DU), or N
cyclohexyl suberogorgamide ( N CS) was injected ip. The AChE
activities in brain hemogenates were determined with colorimetry.
RESULTS: Sub 1 9, Sub DU 3 0, or physostig ̄mine (Phys) 0 15
mg·kg 1 obviously lengthened the SDL by 195 %, 271 %, and 210
%, and shortened the EL by 56 %, 61 %, and 33 %, and the two formers
inhibited the brain AChE activities by 17 % and 19 %, respectively in
aging (3-4 months) mice. These actions were decreased in a dose
dependent manner when Sub or Sub DU was increased to 2 9-4 3 or 4
5-6 7 mg·kg 1 respectively. Sub 1 9, Sub DU 2 0, and Phys
0 15 mg·kg 1 also lengthened the SDL by 187 %, 209 %, and
152 %, and shortened the EL by 52 %, 62 %, and 57 %, respectively in
aged (12-14 months) mice. Sub 1 3-1 9, Sub DU 0 9-2 0, or Phys 0
15 mg·kg 1 reversed the cycloheximide or scopolamine
induced disruptions of memory retention. No obvious effect of N
CS on the acquisition of memory and the AChE activity in mice was
observed. CONCLUSION: The improvements of Sub and Sub DU on memory
were chiefly related to their anti AChE actions.
出处
《中国药理学报》
CSCD
1996年第3期215-218,共4页
Acta Pharmacologica Sinica
关键词
柳珊瑚酸
学习
记忆
胆碱酯酶
抑制剂
衍生物
suberogorgin
N suberogorgamide N N dicyclohexyl urea
N cyclohexyl suberogorga ̄mide
scopolamine
cycloheximide
learning
memory
cholinesterase inhibitors