Manon Gauthier

and 8 more

Background and Purpose Stress is a major risk factor for psychiatric disorders and significantly affects neuroplasticity in brain areas including the nucleus accumbens (NAc) and the insular cortex (IC). Here, we examined alterations in neuroplasticity within the aIC-NAc circuit following restraint stress in male and female rats, and determined the involvement of the endocannabinoid system in this response. Experimental Approach We subjected male and female rats to a 2h-period of acute restraint stress. Following this, we performed behavioral experiments, c-Fos immunohistochemistry and in vivo electrophysiological recordings of NAc neurons in response to aIC stimulation from anesthetized male and female rats immediately and 24h after stress exposure. Since the effect of stress was observed only in males, we evaluated the effects of blockade of cannabinoid CB1 receptors in male rats. Key Results We show that synaptic plasticity in the aIC-NAcC pathway differs between male and female rats. Under basal conditions, in males, long-term potentiation and long-term depression were equally induced, whereas in females, we found mostly a long-term potentiation. Moreover, stress affected synaptic plasticity in the aIC-NAcC only in males, inducing a loss of long-term-depression 24h after stress. Finally, blocking CB1 receptors in males restored long-term depression. Conclusion and Implications These results demonstrate that integration of aIC information to NAcC differs between males and females, that stress affects neuroplasticity only in males, an effect that depends on the endocannabinoid system. This study provides mechanistic support for differential reactivity to stress between males and females that may relate to stress-related psychiatric disorders.

Adelie Salin

and 4 more

Background and Purpose Incubation of craving is associated with temporal changes in the activity of several structures involved in drug-seeking behavior. Hypodopaminergic activity, responsible for negative emotional states, has been reported in the ventral tegmental area (VTA) during cocaine abstinence. The neuroadaptations underlying the VTA hyperdopaminergic state after chronic cocaine is not well understood. In this work, we investigated the potential involvement of a VTA inhibiting circuit (amygdala-ventral pallidum (VP) pathway) in the hypodopaminergic state during abstinence from chronic cocaine. Experimental Approach In a model of cocaine self-administration, we performed in vivo electrophysiological recordings of DA VTA neurons and basolateral amygdala (BLA) neurons from anesthetized rats during early and protracted abstinence and evaluated the involvement of the BLA-VP pathway using a pharmacological approach. Key Results We found a significant decrease of VTA DA population activity and a significant increase of BLA activity after 30 days of abstinence from chronic cocaine but not one day. The decrease in VTA DA activity was restored by pharmacological inhibition of the activity of either the BLA or the VP. Conclusion and Implications Our study sheds new lights on neuroadaptations occurring during incubation of craving leading to relapse. In particular, we described the involvement of the BLA-VP pathway in cocaine-induced decreases of DA activity in the VTA. This study adds an important building block to the characterization of specific brain network dysfunctions underlying hypodopaminergic activity during abstinence.