CHARACTERIZATION OF DELTA-SLEEP-INDUCING PEPTIDE-EVOKED RELEASE OF MET-ENKEPHALIN FROM BRAIN SYNAPTOSOMES IN RATS

被引:2
作者
NAKAMURA, A
SAKAI, K
TAKAHASHI, Y
SHIOMI, H
机构
[1] Department of Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, Hiroshima, Fukuyama
关键词
DELTA-SLEEP-INDUCING PEPTIDE; MET-ENKEPHALIN; LEU-ENKEPHALIN; CALCIUM; TETRODOTOXIN; SYNAPTOSOMES;
D O I
10.1111/j.1471-4159.1991.tb08251.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Delta-sleep-inducing peptide (DSIP) stimulates the release of Met-enkephalin (Met-ENK) from superfused slices of the rodent lower brainstem in vitro. In our present study, DSIP (10(-10)-10(-9) M) induced a significant release of Met-ENK from medullary synaptosomes of rats. This DSIP-evoked release of Met-ENK was Ca2+ dependent and tetrodotoxin (TTX) insensitive. Furthermore, DSIP (10(-11)-10(-9) M) significantly increased (Ca2+)-Ca-45 uptake in medullary synaptosomes. These results demonstrate that DSIP acts directly on the nerve endings of Met-ENK-containing neurons to release this pentapeptide by generating a Ca2+ influx into these neurons. Effects of DSIP on Met-ENK release in other discrete brain regions were also studied. Significant DSIP-evoked Met-ENK release from synaptosomes was observed in the cortex, hypothalamus, and midbrain (at concentrations of 10(-10) and 10(-9) M) and in the hippocampus and thalamus (only at 10(-9) M), but not in the striatum. In the hypothalamus, the release of Leu-enkephalin from its synaptosomes was slightly, but not significantly, enhanced by DSIP (10(-10)-10(-8) M). Our findings demonstrate that DSIP triggered a Ca2+ influx in nerve endings to induce a subsequent release of Met-ENK from neurons in only certain brain regions.
引用
收藏
页码:1013 / 1018
页数:6
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