Yoon Hyung Shin, Kim Seungwoo, Park Hye Kyung, Kim Jeong-Hoon
Department of Physiology, Brain Korea 21 Project for Medical Science, Brain Research Institute, Yonsei University College of Medicine, 134 Shinchondong, Seodaemungu, Seoul 120-752, South Korea.
Neuropharmacology. 2007 Aug;53(2):344-51. doi: 10.1016/j.neuropharm.2007.05.014. Epub 2007 May 29.
The role of the biologically active CART 55-102 peptide in the nucleus accumbens (NAcc) in the expression of cocaine-induced behavioral sensitization was investigated. Rats were divided into four groups: one for saline and the other three for cocaine pre-exposures (15 mg/kg, i.p., once daily for 7 days). After 3 weeks of withdrawal, rats were microinjected into the NAcc either saline or CART 55-102 (1.0, or 2.5 microg/0.5 microl/side) followed by cocaine challenge (10 mg/kg, i.p.). Microinjection into the NAcc of CART 55-102 peptide dose-dependently blocked the expression of locomotor sensitization produced by repeated cocaine pre-exposures. Next, we further examined the effect of CART 55-102 microinjection on extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation levels in the NAcc. Additional four groups of rats were all cocaine pre-exposed and, after 3 weeks of withdrawal, they were either saline or cocaine challenged systemically following microinjection into the NAcc of either saline, CART 55-102 (2.5 microg/0.5 microl/side), or the equivalent mole amount of inactive CART 1-27 peptide. The increase of ERK1/2 phosphorylation levels in the NAcc by cocaine was completely blocked by CART 55-102 microinjection in this site, while it remains unaffected by inactive CART 1-27 peptide. These results suggest that CART 55-102 peptide in the NAcc may play a compensatory inhibitory role in the expression of behavioral sensitization by cocaine and these effects may be mediated by its inhibition of ERK1/2 phosphorylation in this site.
研究了伏隔核(NAcc)中具有生物活性的可卡因-安非他明调节转录肽(CART)55-102肽在可卡因诱导的行为敏化表达中的作用。将大鼠分为四组:一组注射生理盐水,另外三组进行可卡因预暴露(15mg/kg,腹腔注射,每天一次,共7天)。撤药3周后,向大鼠伏隔核中微量注射生理盐水或CART 55-102(1.0或2.5μg/0.5μl/侧),随后进行可卡因激发(10mg/kg,腹腔注射)。向伏隔核中微量注射CART 55-102肽可剂量依赖性地阻断重复可卡因预暴露所产生的运动敏化表达。接下来,我们进一步研究了微量注射CART 55-102对伏隔核细胞外信号调节激酶1/2(ERK1/2)磷酸化水平的影响。另外四组大鼠均进行可卡因预暴露,撤药3周后,在向伏隔核中微量注射生理盐水、CART 55-102(2.5μg/0.5μl/侧)或等量摩尔量的无活性CART 1-27肽后,对其进行全身生理盐水或可卡因激发。在此部位,可卡因引起的伏隔核中ERK1/2磷酸化水平升高被CART 55-102微量注射完全阻断,而无活性的CART 1-27肽对其无影响。这些结果表明,伏隔核中的CART 55-102肽可能在可卡因诱导的行为敏化表达中起代偿性抑制作用,且这些作用可能是通过其对该部位ERK1/2磷酸化的抑制来介导的。