Mianserin, but not Ondansetron, reduces the locomotor stimulating effect of ethanol in preweanling rats

被引:2
作者
Arias, Carlos [1 ]
Spear, Norman E.
机构
[1] INIMEC CONICET, Inst Invest Med M&M Ferreyra, RA-5000 Cordoba, Argentina
关键词
Ethanol; Rat; Infancy; Locomotor stimulation; Serotonin; Mianserin; Ondansetron; CONDITIONED PLACE PREFERENCE; SPRAGUE-DAWLEY RATS; RECEPTOR ANTAGONIST; OPIOID RECEPTORS; MICE; SENSITIZATION; EXPRESSION; BLOCKS; SENSITIVITY; INVOLVEMENT;
D O I
10.1016/j.pbb.2011.07.016
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
During infancy rats are highly sensitive to the locomotor stimulating effect of ethanol, an effect particularly observed when they are tested during the rising phase of the blood ethanol curve and in a novel environment. According to a recent study infant rats require some degree of stress to get stimulated after being challenged with ethanol. Ethanol-induced stimulation in preweanling rats required the activation of CRH-1 receptors. Considering these antecedents, we explored modulation of the acute stimulating effect of ethanol (2.5 g/kg) by two anxiolytic drugs, Mianserin (2.5 or 5 mg/kg) and Ondansetron (1 or 3 mg/kg). Mianserin attenuated the stimulating effect of ethanol at a dose that did not affect locomotor activity in water-controls, likely acting through 5-HT2 receptors, while Ondansetron, a 5-HT3 antagonist, did not affect this response. These results are consistent with recent findings indicating that one of the mechanisms by which the CRH-1 receptor modulates anxiety depends on sensitization of the 5-HT2 receptor antagonist, and highlight the importance of stress as a modulator of the effects of ethanol during early developmental stages. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 85
页数:5
相关论文
共 28 条
  • [11] ANTI-DEPRESSANT DRUGS AND ETHANOL - BEHAVIORAL AND PHARMACOKINETIC INTERACTIONS IN MICE
    COTT, JM
    OGREN, SO
    [J]. JOURNAL OF NEURAL TRANSMISSION, 1980, 48 (04) : 223 - 240
  • [12] Darmani NA, 1999, J PHARMACOL EXP THER, V288, P247
  • [13] Corticotropin releasing factor-1 receptor antagonist, CP-154,526, blocks the expression of ethanol-induced behavioral sensitization in DBA/2J mice
    Fee, J. R.
    Sparta, D. R.
    Picker, M. J.
    Thiele, T. E.
    [J]. NEUROSCIENCE, 2007, 150 (01) : 14 - 21
  • [14] Serotonin 5-HT2 receptor antagonist does not reverse established ethanol-induced sensitization but blocks its development and expression
    Ferraz, I. C.
    Boerngen-Lacerda, R.
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2008, 88 (04) : 456 - 464
  • [15] m-CPP hypolocomotion is selectively antagonized by compounds with high affinity for 5HT2C receptors but not 5-HT2A or 5-HT2B receptors
    Gleason, SD
    Lucaites, VL
    Shannon, HE
    Nelson, DL
    Leander, JD
    [J]. BEHAVIOURAL PHARMACOLOGY, 2001, 12 (08): : 613 - 620
  • [16] PRINCIPLES AND PITFALLS IN THE ANALYSIS OF PRENATAL TREATMENT EFFECTS IN MULTIPAROUS SPECIES
    HOLSON, RR
    PEARCE, B
    [J]. NEUROTOXICOLOGY AND TERATOLOGY, 1992, 14 (03) : 221 - 228
  • [17] Effects of 5-HT3, D-1 and D-2 receptor antagonists on ethanol- and cocaine-induced locomotion
    Le, AD
    Tomkins, D
    Higgins, G
    Quan, B
    Sellers, EM
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1997, 57 (1-2) : 325 - 332
  • [18] CRF receptor 1 regulates anxiety behavior via sensitization of 5-HT2 receptor signaling
    Magalhaes, Ana C.
    Holmes, Kevin D.
    Dale, Lianne B.
    Comps-Agrar, Laetitia
    Lee, Dennis
    Yadav, Prem N.
    Drysdale, Linsay
    Poulter, Michael O.
    Roth, Bryan L.
    Pin, Jean-Philippe
    Anisman, Hymie
    Ferguson, Stephen S. G.
    [J]. NATURE NEUROSCIENCE, 2010, 13 (05) : 622 - U140
  • [19] THE EXCITATORY EFFECT OF ETHANOL - ABSENCE IN RATS, NO TOLERANCE AND INCREASED SENSITIVITY IN MICE
    MASUR, J
    DESOUZA, MLO
    ZWICKER, AP
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1986, 24 (05) : 1225 - 1228
  • [20] Miller S. S., 2009, 34 ANN SCI M RES SOC