scholarly journals The anterior insular cortex in the rat exerts an inhibitory influence over the loss of control of heroin intake and subsequent propensity to relapse

2020 ◽  
Author(s):  
Dhaval D. Joshi ◽  
Mickaël Puaud ◽  
Maxime Fouyssac ◽  
Aude Belin-Rauscent ◽  
Barry Everitt ◽  
...  

AbstractThe anterior insular cortex (AIC) has been implicated in addictive behaviour, including the loss of control over drug intake, craving and the propensity to relapse. Evidence suggests that the influence of the AIC on drug-related behaviours is complex since in rats exposed to extended access to cocaine self-administration, the AIC was shown to exert a state-dependent, bidirectional influence on the development and expression of loss of control over drug intake, facilitating the latter but impairing the former. However, it is unclear whether this influence of the AIC is confined to stimulant drugs that have marked peripheral sympathomimetic and anxiogenic effects or whether it extends to other addictive drugs, such as opiates, that lack overt acute aversive peripheral effects. Thus, we investigated in outbred rats the effects of bilateral excitotoxic lesions of AIC, induced both prior to or after long-term exposure to extended access heroin self-administration, on the development and maintenance of escalated heroin intake and the subsequent vulnerability to relapse following abstinence. Compared to sham-surgeries, pre-exposure AIC lesions had no effect on the development of loss of control over heroin intake, but lesions made after a history of escalated heroin intake potentiated escalation and also enhanced responding at relapse. These data show that the AIC inhibits or limits the loss of control over heroin intake and propensity to relapse, in marked contrast to its influence on the loss of control over cocaine intake.

2020 ◽  
Vol 52 (9) ◽  
pp. 4115-4126 ◽  
Author(s):  
Dhaval D. Joshi ◽  
Mickaël Puaud ◽  
Maxime Fouyssac ◽  
Aude Belin‐Rauscent ◽  
Barry Everitt ◽  
...  

Neuroscience ◽  
2020 ◽  
Vol 443 ◽  
pp. 93-109
Author(s):  
Peter U. Hámor ◽  
Mariola J. Edelmann ◽  
Christina Gobin ◽  
Marek Schwendt

2020 ◽  
Vol 27 (4) ◽  
pp. 14-17
Author(s):  
Heidar Mohammadjafari ◽  
Hamid Arazi ◽  
Nematollah Nemati ◽  
Tahereh Bagherpoor

Abstract Introduction. Some athletes and non-athletes use peptide hormones to increase lean body mass and fat loss, but those effects on oxidative stress and antioxidant markers are unknown. The aim of this study was to show the physiological profile of oxidative stress and antioxidant markers in athletes and non-athletes following long-term self-administration of GH or IGF-1 Material and Methods. Seventy-five healthy young men with the history of peptide hormone (i.e., GH or IGF-1) use for at least 1 year (i.e., 3 to 4 times a year) or resistance exercise (RE) experience for at least 3 years volunteered to participate in this study and were divided into 5 selected groups including 1) GH use plus RE (GH+RE, n = 15), 2) IGF-1 use plus RE (IGF-1+RE, n = 15), 3) GH use (GH, n = 15), 4) IGF-1 use (IGF-1, n = 15), and 5) RE only (RE, n = 15). Blood sample was obtained one time in order to evaluate the resting concentration of oxidative stress markers including 8-hydroxy-2-deoxyguanosine (8-OHdG), malondialdehyde (MDA), nitric oxide (NO) and antioxidant defense systems (i.e., glutathione peroxidase [GPx], catalase [CAT], and glutamate [GLU]). Results. There were no significant (p > 0.05) differences among the groups in the 8-OHdG, MDA, NO, GPx, CAT, and GLU levels. Conclusions. Self-administration of peptide hormone and RE for at least 1 year is not accompanied by alterations in resting oxidative stress and the antioxidant system in male athletes and non-athletes.


2015 ◽  
Vol 20 (5) ◽  
pp. 913-926 ◽  
Author(s):  
Daniele Caprioli ◽  
Tamara Zeric ◽  
Eric B. Thorndike ◽  
Marco Venniro

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