Withdrawal-induced short-term increase in voluntary intake of diazepam in mice is not a stable group characteristics

Abstract

We investigated the involvement of alpha-melanocyte stimulating hormone (α-MSH) following acute, chronic and withdrawal treatments of ethanol with reference to depression. The degree of depression was evaluated using Porsolt's forced swim test. While intracerebroventricular (icv) α-MSH (100–400 ng/rat) dose-dependently increased the immobility, opposite response was observed following administration of selective MC4 receptor antagonist HS014 (0.01–0.07 ng/rat, icv). The anti-immobility effect of acute ethanol (1–2 g/kg), injected via intra-peritoneal route (ip), was suppressed by central administration of α-MSH (100 ng/rat, icv), but was enhanced following pretreatment with HS014 (0.01 ng/rat, icv). Chronic ethanol resulted in increased immobility time, while further augmentation in immobility was noticed following ethanol withdrawal. However, concomitant HS014 (0.01 ng/rat, icv) treatment prevented tolerance as well as attenuated enhanced immobility in ethanol-withdrawn rats. Acute administration of HS014 (0.01–0.03 ng/rat, icv), at 24h post-withdrawal time point, also antagonized the ethanol withdrawal immobility in rats.The profile of α-MSH-immunoreactivity in the paraventricular (PVN), arcuate (ARC), paraventricular thalamic (PVT), dorsomedial hypothalamic-dorsal (DMNd) and -ventral (DMNv) nuclei, lateral hypothalamus (LH) and central nucleus of amygdala (CeA) was investigated with immunocytochemistry. Acute ethanol significantly reduced the α-MSH-immunoreactivity in the cells and fibers of ARC, and fibers in the PVN, DMNd, DMNv and CeA. While chronic ethanol treatment significantly increased the α-MSH-immunoreactivity as compared to the pair-fed control group, further augmentation was noticed following 24 h ethanol withdrawal. However, the α-MSH-immunoreactive profile in the PVT and LH did not respond. α-MSH in discrete areas may play a role in ethanol-induced antidepressant-like response and withdrawal-induced depression.