Cryan John F, Page Michelle E, Lucki Irwin
Department of Psychiatry, University of Pennsylvania, 538A Clinical Research Building, 415 Curie Boulevard, Philadelphia, PA 19104, USA.
Eur J Pharmacol. 2002 Feb 2;436(3):197-205. doi: 10.1016/s0014-2999(01)01628-4.
The novel antidepressant reboxetine is a selective norepinephrine reuptake inhibitor. In this study, the antidepressant-like effects of reboxetine were characterized in a modified rat forced swim test. Further, in order to investigate the role of the locus coeruleus and lateral tegmental noradrenergic systems in the mediation of reboxetine's effects, the impact of different chemical lesions of these two pathways was examined on the behavioral responses induced by reboxetine in the forced swim test. Reboxetine (5-20 mg/kg, s.c.) dose-dependently decreased immobility and swimming behavior in the forced swim test while it simultaneously increased climbing behavior. These effects were similar to those previously demonstrated with tricyclic antidepressants and are indicative of reboxetine's effects on the noradrenergic system. Discrete local injections of the neurotoxin 6-hydroxydopamine were employed to lesion the ventral noradrenergic bundle arising from cells located in the lateral tegmentum. This resulting lesion completely prevented reboxetine (10 mg/kg, s.c.)-induced decreases in immobility and increases in climbing behavior, demonstrating that an intact ventral noradrenergic bundle is required for the manifestation of reboxetine-induced antidepressant-like behavior in the test. In contrast, lesions of the dorsal noradrenergic bundle which consists of neurons arising from the nucleus locus coereleus, were achieved by systemic pretreatment with the selective noradrenergic neurotoxin N-(2-chloroethyl)-N-2-bromobenzylamine (DSP-4; 50 mg/kg, i.p.). The ability of reboxetine (10 mg/kg, s.c.) to increase climbing and decrease immobility was augmented by DSP-4 pretreatment. Furthermore, neither lesions of the dorsal noradrenergic bundle nor the ventral noradrenergic bundle altered baseline immobility scores in the forced swim test. Taken together, these data suggest that forebrain regions innervated by these two distinct noradrenergic pathways exert opposing influences on the behavioral response to reboxetine in the rat forced swim test.
新型抗抑郁药瑞波西汀是一种选择性去甲肾上腺素再摄取抑制剂。在本研究中,通过改良的大鼠强迫游泳试验对瑞波西汀的抗抑郁样作用进行了表征。此外,为了研究蓝斑和外侧被盖去甲肾上腺素能系统在介导瑞波西汀作用中的作用,考察了这两条通路不同化学损伤对瑞波西汀在强迫游泳试验中诱导的行为反应的影响。瑞波西汀(5 - 20毫克/千克,皮下注射)在强迫游泳试验中剂量依赖性地减少不动时间和游泳行为,同时增加攀爬行为。这些作用与先前用三环类抗抑郁药所证明的作用相似,表明瑞波西汀对去甲肾上腺素能系统有作用。采用离散局部注射神经毒素6 - 羟基多巴胺来损伤起源于外侧被盖区细胞的腹侧去甲肾上腺素能束。这种损伤完全阻止了瑞波西汀(10毫克/千克,皮下注射)诱导的不动时间减少和攀爬行为增加,表明完整的腹侧去甲肾上腺素能束是瑞波西汀在该试验中诱导抗抑郁样行为表现所必需的。相反,由蓝斑核神经元组成的背侧去甲肾上腺素能束的损伤是通过用选择性去甲肾上腺素能神经毒素N -(2 - 氯乙基)- N - 2 - 溴苄胺(DSP - 4;50毫克/千克,腹腔注射)进行全身预处理来实现的。DSP - 4预处理增强了瑞波西汀(10毫克/千克,皮下注射)增加攀爬和减少不动的能力。此外,背侧去甲肾上腺素能束或腹侧去甲肾上腺素能束的损伤均未改变强迫游泳试验中的基线不动评分。综上所述,这些数据表明,由这两条不同的去甲肾上腺素能通路支配的前脑区域对大鼠强迫游泳试验中对瑞波西汀的行为反应产生相反的影响。