Influence of PCPA and MDMA (ecstasy) on physiology, development and behavior in Drosophila melanogaster

被引:28
作者
Dasari, Sameera
Viele, Kert
Turner, A. Clay
Cooper, Robin L.
机构
[1] Univ Kentucky, Dept Biol, Lexington, KY 40506 USA
[2] Univ Kentucky, Dept Stat, Lexington, KY 40506 USA
关键词
CNS; dopamine; drugs of abuse; ecstasy; MDMA; PCPA; synapse;
D O I
10.1111/j.1460-9568.2007.05655.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of para-chlorophenylalanine (PCPA) and 3,4 methylenedioxy-methamphetamine (MDMA, 'ecstasy') were investigated in relation to development, behavior and physiology in larval Drosophila. PCPA blocks the synthesis of serotonin (5-HT) and MDMA is known to deplete 5-HT in mammalian neurons; thus these studies were conducted primarily to target the serotonergic system. Treatment with PCPA and MDMA delayed time to pupation and eclosion. The developmental rate was investigated with a survival analysis statistical approach that is unique for Drosophila studies. Locomotion and eating were reduced in animals exposed to MDMA or PCPA. Sensitivity to exogenously applied 5-HT on an evoked sensory-central nervous system (CNS)-motor circuit showed that the CNS is sensitive to 5-HT but that when depleted of 5-HT by PCPA a decreased sensitivity occurred. A diet with MDMA produced an enhanced response to exogenous 5-HT on the central circuit. Larvae eating MDMA from the first to third instar did not show a reduction in 5-HT within the CNS; however, eating PCPA reduced 5-HT as well as dopamine content as measured by high performance liquid chromatography from larval brains. As the heart serves as a good bioindex of 5-HT exposure, it was used in larvae fed PCPA and MDMA but no significant effects occurred with exogenous 5-HT. In summary, the action of these pharmacological compounds altered larval behaviors and development. PCPA treatment changed the sensitivity in the CNS to 5-HT, suggesting that 5-HT receptor regulation is modulated by neural activity of the serotonergic neurons. The actions of acute MDMA exposure suggest a 5-HT agonist action or possible dumping of 5-HT from neurons.
引用
收藏
页码:424 / 438
页数:15
相关论文
共 96 条
[1]  
ARECHIGA H, 1980, FRONT HORM RES, V6, P16
[2]   Rapid desensitization of somatodendritic 5-HT1A receptors by chronic administration of the high-efficacy 5-HT1A agonist, F13714:: a microdialysis study in the rat [J].
Assie, M-B ;
Lomenech, H. ;
Ravailhe, V. ;
Faucillon, V. ;
Newman-Tancredi, A. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 149 (02) :170-178
[3]   5-HT2A receptor gene polymorphism is associated with food and alcohol intake in obese people [J].
Aubert, R ;
Betoulle, D ;
Herbeth, B ;
Siest, G ;
Fumeron, F .
INTERNATIONAL JOURNAL OF OBESITY, 2000, 24 (07) :920-924
[4]  
Ayali A, 1999, J NEUROSCI, V19, P6712
[5]   A review of central 5-HT receptors and their function [J].
Barnes, NM ;
Sharp, T .
NEUROPHARMACOLOGY, 1999, 38 (08) :1083-1152
[6]  
Bicker G, 1999, MICROSC RES TECHNIQ, V44, P166, DOI 10.1002/(SICI)1097-0029(19990115/01)44:2/3<166::AID-JEMT8>3.0.CO
[7]  
2-T
[8]   Molecular and pharmacological properties of insect biogenic amine receptors:: Lessons from Drosophila melanogaster and Apis mellifera [J].
Blenau, W ;
Baumann, A .
ARCHIVES OF INSECT BIOCHEMISTRY AND PHYSIOLOGY, 2001, 48 (01) :13-38
[9]  
Campos-Ortega J.A., 1985, EMBRYONIC DEV DROSOP, P3, DOI 10.1007/978-3-662-02454-6_2
[10]   Single exposure to a serotonin 1A receptor agonist, (+) 8-hydroxy-2-(di-n-propylamino)-tetralin, produces a prolonged heterologous desensitization of serotonin 2A receptors in neuroendocrine neurons in vivo [J].
Carrasco, Gonzalo A. ;
Van de Kar, Louis D. ;
Jia, Cuihong ;
Xu, Hao ;
Chen, Zhuo ;
Chadda, Ritu ;
Garcia, Francisca ;
Muma, Nancy A. ;
Battaglia, George .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 320 (03) :1078-1086