The activity of CART peptide fragments

被引:42
作者
Dylag, Tomasz
Kotlinska, Jolanta
Rafalski, Piotr
Pachuta, Agnieszka
Silberring, Jerzy
机构
[1] Jagiellonian Univ, Fac Chem, Dept Neurobiochem, PL-30060 Krakow, Poland
[2] Jagiellonian Univ, Reg Lab, PL-30060 Krakow, Poland
[3] Med Univ Lublin, Dept Pharmacodynam, PL-20081 Lublin, Poland
[4] Polish Acad Sci, Ctr Polymer Chem, PL-41819 Zabrze, Poland
关键词
CART; fragment; cocaine; amphetamine; morphine; dependence; sensitization;
D O I
10.1016/j.peptides.2005.10.025
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
Cocaine- and amphetamine-regulated transcript (CART) peptides attracted much attention after the discovery that the level of CART mRNA is increased in rat striatum after acute administration of cocaine and amphetamine. The most widely investigated sequence is CART (55-102), whose roles were confirmed in modulation of various physiological processes such as feeding, energy expenditure, stress control, endocrine secretion, and reward. However, peptides other than (55-102) may be generated from the CART precursor as well. This review describes biological activity of peptides derived from the CART precursor in vivo, and of synthetic CART fragments that have not been found in the nature. In particular, the activity of CART (85-102) is described, whose ability to exert behavioral responses was confirmed by the observed attenuation of the expression of sensitization to morphineinduced hyperlocomotion. This fragment also decreased the number of escape jumps evoked by naloxone in morphine-addicted mice after intracerebroventricular administration. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1926 / 1933
页数:8
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