Effect of chronic m-CPP on locomotion, hypophagia, plasma corticosterone and 5-HT2C receptor levels in the rat

被引:62
作者
Fone, KCF [1 ]
Austin, RH
Topham, IA
Kennett, GA
Punhani, T
机构
[1] Univ Nottingham, Sch Med, Queens Med Ctr, Sch Biomed Sci, Nottingham NG7 2UH, England
[2] SmithKline Beecham Pharmaceut, Psychiat Res, Harlow CM19 5AW, Essex, England
关键词
5-hydroxytryptamine(2C) receptors; hypolocomotion; hypophagia; 5-hydroxytryptamine(2C) antibodies; corticosterone; anxiety;
D O I
10.1038/sj.bjp.0701798
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 The present study examined 5-HT2C receptor agonist-induced behavioural tolerance and 5-HT2C receptor down-regulation in adult rat brain. The effect of chronic subcutaneous infusion of the 5-HT2C receptor agonist, m-chlorophenylpiperazine (m-CPP, 10 mg kg(-1), day(-1)), for 14 days was examined on daily food intake, the ability of acute m-CPP (2.5 mg kg(-1), i.p.) to induce hypolocomotion in a novel arena and elevate plasma corticosterone levels and on ex vivo cortical [H-3]-mesulergine binding and hippocampal 5-HT2C receptor protein levels. 2 Before chronic infusion, m-CPP (2.5 mg kg(-1), i.p.) attenuated the number of turns and rears made in a navel open field arena. In contrast, while m-CPP still elicited this hypolocomotion following 14 days, saline infusion, no such hypolocomotion occurred in rats given chronic m-CPP (10 mg kg(-1) day(-1)), indicating that almost complete tachyphylaxis of this behaviour occurred with chronic 5-HT2C receptor agonist injection. 3 During chronic infusion of m-CPP, rats consumed less food per day than saline-treated controls. Acute challenge with m-CPP following two weeks, treatment still attenuated food intake over the next four hours (by 43% and 30%, respectively from that on the previous day) in saline and m-CPP infusion groups, showing that only partial tolerance to 5-HT2C receptor agonist-induced hypophagia occurred. 4 In naive home cage rats, plasma corticosterone was elevated in a dose-dependent manner 35 min after m-CPP injection (0.5, 1 and 3 mg kg(-1), i.p.) but levels were comparable to control values 16 h after m-CPP (2, 5 and 10 mg kg(-1), i.p.). Sixteen hours after a single m-CPP injection (2.5 mg kg(-1), i.p.), plasma corticosterone levels were comparable in a group of rats which had received 14 days infusion of m-CPP or saline. However, following a similar acute m-CPP injection (2.5 mg kg(-1), i.p., -16 h) in rats previously infused for 14 days with m-CPP, plasma corticosterone levels were lower than those in a separate group which received no chronic infusions (but only acute m-CPP injection), even though the plasma m-CPP levels were comparable in both groups. The data are consistent with the proposal that chronic m-CPP induced some down-regulation of hypothalamic 5-HT2C receptors which contribute, in a tonic manner, to plasma corticosterone secretion under the conditions investigated. 5 Chronic m-CPP infusion reduced the amount of [H-3]-mesulergine binding (by 27%, without altering the K-D) in membranes prepared from parietal/occipital/temporal cortex (under conditions to exclude binding to 5-HT2A receptors) and 5-HT2C receptor protein-like immunoreactive levels measured by radioimmunoassay in the hippocampus by 38%, confirming that 5-HT2C receptor down-regulation had occurred. 6 Even after 14 days m-CPP infusion only partial behavioural tolerance and 5-HT2C receptor downregulation were observed, which may vary in different brain regions of the rat. Thus the hypophagia produced by m-CPP may involve activation of 5-HT2C receptors in the hypothalamus, where there is a greater receptor reserve or which are more resistant to agonist-induced down-regulation than 5-HT2C receptors in limbic areas (striatum and nucleus accumbens) mediating m-CPP-induced hypolocomotion.
引用
收藏
页码:1707 / 1715
页数:9
相关论文
共 56 条
[1]  
Bagdy G, 1996, BEHAV BRAIN RES, V73, P277
[2]   5-HT2 RECEPTOR SUBTYPES - A FAMILY RE-UNITED [J].
BAXTER, G ;
KENNETT, G ;
BLANEY, F ;
BLACKBURN, T .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1995, 16 (03) :105-110
[3]   ATTENUATION OF 5-HT1A AND 5-HT2 BUT NOT 5-HT1C RECEPTOR MEDIATED BEHAVIOR IN RATS FOLLOWING CHRONIC TREATMENT WITH 5-HT RECEPTOR AGONISTS, ANTAGONISTS OR ANTI-DEPRESSANTS [J].
BERENDSEN, HHG ;
BROEKKAMP, CLE .
PSYCHOPHARMACOLOGY, 1991, 105 (02) :219-224
[4]   ADAPTIVE-CHANGES IN THE 5-HT2 BINDING-SITE AFTER CHRONIC ADMINISTRATION OF AGONISTS AND ANTAGONISTS [J].
BLACKSHEAR, MA ;
MARTIN, LL ;
SANDERSBUSH, E .
NEUROPHARMACOLOGY, 1986, 25 (11) :1267-1271
[5]   RS-102221: A novel high affinity and selective, 5-HT2C receptor antagonist [J].
Bonhaus, DW ;
Weinhardt, KK ;
Taylor, M ;
Desouza, A ;
Mcneeley, PM ;
Szczepanski, K ;
Fontana, DJ ;
Trinh, J ;
Rocha, CL ;
Dawson, MW ;
Flippin, LA ;
Eglen, RM .
NEUROPHARMACOLOGY, 1997, 36 (4-5) :621-629
[6]   5-HT4, 5-HT6, 5-HT7; Molecular pharmacology of adenylate cyclase stimulating receptors [J].
Branchek, TA .
SEMINARS IN THE NEUROSCIENCES, 1995, 7 (06) :375-382
[7]   Regulation of serotonin-2C receptor G-protein coupling by RNA editing [J].
Burns, CM ;
Chu, H ;
Rueter, SM ;
Hutchinson, LK ;
Canton, H ;
SandersBush, E ;
Emeson, RB .
NATURE, 1997, 387 (6630) :303-308
[8]   MECHANISMS OF SEROTONIN RECEPTOR AGONIST-INDUCED ACTIVATION OF THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS IN THE RAT [J].
CALOGERO, AE ;
BAGDY, G ;
SZEMEREDI, K ;
TARTAGLIA, ME ;
GOLD, PW ;
CHROUSOS, GP .
ENDOCRINOLOGY, 1990, 126 (04) :1888-1894
[9]  
Canton H, 1996, MOL PHARMACOL, V50, P799
[10]   LONG-TERM CLORGYLINE TREATMENT ANTAGONIZES THE EATING AND MOTOR FUNCTION RESPONSES TO META-CHLOROPHENYLPIPERAZINE [J].
COHEN, RM ;
AULAKH, CS ;
MURPHY, DL .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1983, 94 (1-2) :175-179