摘要
本文采用淋巴细胞转化(淋转)试验法观察到β-内啡肽在浓度为0.3,3,30nmol/L时,可增强亚适量刀豆蛋白A(ConA)(0.625mg/L)诱导的小鼠脾淋转反应,而对未经活化的静止淋巴细胞未见致分裂作用。作者又观察到纳洛酮作为阿片受体的拮抗剂,可阻断β-内啡肽对小鼠脾淋转反应的增强作用。另外,发现在ConA诱导淋转过程中不同时间加入β-内啡肽,其协同效应从培养起始后24h内最为明显。
Using lymphocyte transformation test as an indioator,we investigated the regulatory effect of β-endorphin on splenocyte proliferation in mice.The results showed that β-endorphin in doses of 0.3,3,30 nmol/L enhanced the proliferation response of splenocytes to Con A in a suboptimal concentration(0.625 mg/L)but did not have any effect on resting,unstimulated spleen cells.The maximal effect of β-endorphin on lymphocyte proliferation was seen when it was added to the experimental system within 24 hours after the commencement of culture.The effect of β-endorphin is reversed by naloxone,an opiate peptide antagonist.
出处
《上海医科大学学报》
CSCD
1994年第3期182-186,共5页
Journal of Fudan University(Medical Science)
关键词
β
内啡肽
脾
淋巴细胞
β-endorphin
Con A:mouse splencoyte
naloxone
ymphocyte transformation test