Brown Zenya J, Tribe Erin, D'souza Nicole A, Erb Suzanne
Centre for the Neurobiology of Stress, Department of Psychology, University of Toronto Scarborough, 1265 Military Trail, Toronto, ON, M1C 1A4, Canada.
Psychopharmacology (Berl). 2009 Mar;203(1):121-30. doi: 10.1007/s00213-008-1376-4. Epub 2008 Nov 5.
Corticotropin-releasing factor (CRF) and noradrenaline (NA) have been shown in independent studies to mediate stress-induced reinstatement of drug seeking. To date, however, a functional interaction between the systems in reinstatement has not been demonstrated.
The objectives of this study were to determine whether CRF and NA systems can interact to influence reinstatement responding and, if so, in what direction the interaction occurs.
Rats were trained to self-administer cocaine (0.23 mg/kg per infusion) for 8-10 days. Subsequently, responding for drug was extinguished, and tests for reinstatement were conducted following: (1) pretreatment with the CRF receptor antagonist, D: -Phe CRF(12-41) [1 microg, intracerebroventricular (i.c.v.)], prior to i.c.v. injections of NA (10 microg; Experiment 1); (2) pretreatment with the alpha(2) adrenoceptor agonist, clonidine (40 microg/kg, i.p.), prior to i.c.v. injections of CRF (0.5 microg; Experiment 2); (3) pretreatment with D: -Phe (1, 5 microg, i.c.v.), prior to systemic injections of the alpha(2) adrenoceptor antagonist, yohimbine (1.25 mg/kg; Experiment 3A); or (4) pretreatment with clonidine (40 microg/kg, i.p.) prior to systemic injections of yohimbine (0.625 mg/kg, 1.25 mg/kg; Experiment 3B).
NA reliably induced reinstatement, an effect that was blocked by pretreatment with D: -Phe. In contrast, CRF-induced reinstatement was not attenuated by pretreatment with clonidine. Pretreatment with neither D: -Phe nor clonidine was effective in blocking yohimbine-induced reinstatement.
Together, the present findings suggest a functional interaction between NA and CRF systems in mediating stress-induced reinstatement of cocaine seeking, whereby activation of CRF receptors occurs subsequent to, and downstream of, the sites of action of NA.
在独立研究中已表明促肾上腺皮质激素释放因子(CRF)和去甲肾上腺素(NA)介导应激诱导的觅药行为复燃。然而,迄今为止,尚未证实这两个系统在复燃过程中存在功能相互作用。
本研究的目的是确定CRF和NA系统是否能相互作用以影响复燃反应,如果可以,相互作用的方向是什么。
训练大鼠自我注射可卡因(每次注射0.23mg/kg),持续8 - 10天。随后,停止对药物的反应,并在以下情况下进行复燃测试:(1)在脑室内注射NA(10μg)之前,预先脑室内注射CRF受体拮抗剂D - Phe CRF(12 - 41)(1μg;实验1);(2)在脑室内注射CRF(0.5μg)之前,腹腔注射α₂肾上腺素能受体激动剂可乐定(40μg/kg;实验2);(3)在全身注射α₂肾上腺素能受体拮抗剂育亨宾(1.25mg/kg)之前,预先脑室内注射D - Phe(1、5μg;实验3A);或(4)在全身注射育亨宾(0.625mg/kg、1.25mg/kg)之前,腹腔注射可乐定(40μg/kg;实验3B)。
NA可靠地诱导了复燃,D - Phe预处理可阻断此效应。相反,可乐定预处理并未减弱CRF诱导的复燃。D - Phe和可乐定预处理均不能有效阻断育亨宾诱导的复燃。
总体而言,目前的研究结果表明NA和CRF系统在介导应激诱导的可卡因觅药行为复燃中存在功能相互作用,即CRF受体的激活发生在NA作用位点之后且在其下游。