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Gonzalez, I. L.

Publications and source records attributed to Gonzalez, I. L..

3 recordsLinked to original sources

Effects of Social Housing on Electrically Stimulated Dopamine Release in the Nucleus Accumbens Core and Shell in Female and Male Rats

Dopamine (DA) is a neurotransmitter that is important in the reward system and increased DA release is associated with rewarding properties of drugs. Highly addictive stimulants like methamphetamine (METH) increase DA release and block reuptake, causing the DA to stay in the synapse longer, enhancing its effects. Because the misuse of METH is increasing in the United States, it is important to investigate ways to protect against this highly addictive stimulant. Recent studies have shown that social support can be a protective factor against METH self-administration in females, but not males. Other studies using microdialysis have shown that socially housed females have lower DA release in the nucleus accumbens (NAc) compared to single housed females after treatment with METH. Additionally, researchers have shown that there are sex differences in stimulated DA release. The present study investigates whether social housing affects stimulated DA release after METH treatment. DA release in the NAc core and shell of socially housed and individually housed rats was measured using fast scan cyclic voltammetry (FSCV) with a chronic 16-channel carbon fiber electrode in the NAc. A stimulating electrode was aimed at the ventral tegmental area (VTA) to induce DA release in the NAc. The results showed that social housing enhances electrically stimulated DA release in males and that there was greater DA release in NAc core than shell in single males, but no difference in socially housed males. In females, social housing also enhanced ES DA release. In single females there was greater ES DA release in shell than in core. Additionally, in single housed females there was greater ES DA release over time, while the socially housed females had high ES DA release that remained stable over time. These results suggest that social housing protects females from sensitization, making single females more vulnerable to the addictive properties of METH.

neuroscience↗

Social housing effects of Intermittent Access of Methamphetamine Self-administration and social behavior

Social support is a potentially protective factor against substance use disorders (SUDs). Previous studies in animal models for SUDs have shown that when females are pair housed, they have lower motivation for cocaine and methamphetamine (METH) than females who are single housed. In males, however, social housing has not had the same beneficial effect. This study investigates effects of social housing on METH self-administration in females or males when both cage mates are self-administering METH. The study also investigated how the quality of the relationships changed after METH self-administration. The results show that singly housed females self-administered more METH than socially housed females, while males in both social housing conditions self-administered METH at the same rate. The social behavior data showed that females given saline spent more time apart, however the females given METH spent more time together, suggesting that their social behavior may play a role in the attenuation of METH self-administration. Males social behavior remained unchanged after METH and the dominant male in a pair self-administered more METH than the non-dominant male. Females self-administration was not affected by dominance. The results of this study show that social housing provides some protective benefits to females, but not males, for METH self-administration. Further, the type of relationship between cage mates affects males self-administration and may explain why social housing with a same sex mate is not beneficial for males. STRUCTURED ABSTRACT BackgroundSocial support is a potentially protective factor against substance use disorders (SUDs). Previous studies in rats have shown that when females are pair housed, they have lower motivation for drugs such as cocaine and methamphetamine (METH), than females who are single housed. In males, however, socially housed and singly housed males both have the same motivation for drugs such as cocaine. PurposeThe aim of this study was to investigate if social housing would attenuate METH self-administration in females or males when both cage mates are self-administering METH on an intermittent access schedule (IntA). The study also investigated how the quality of those relationships changed after METH self-administration, if dominance played a role in the rate of self-administration, and the extent to which the quality of the relationships was related to METH self-administration. MethodsMale and female rats were individually housed or housed in same sex pairs from around day 42, then animals underwent self-administration of METH (0.3 mg/kg/inf) on an IntA schedule of reinforcement. Both animals in a pair self-administered METH. Social behavior was evaluated prior to and throughout the period when animals were self-administering METH. ResultsThe results showed that in females, single housed females self-administered more METH than pair housed females, while males in both housing conditions self-administered METH at the same rate. More singly housed females on day one of the IntA had high rates of self-administration, compared to socially housed females. Differences attenuated after the first session, but singly housed females still self-administered METH to a greater extent than pair housed females overall. The social behavior data showed that females given saline spent more time apart while the females given METH spent more time together. This suggested that social behavior may contribute to the attenuation of self-administration in females. Males social behavior largely remained unchanged after METH and males continued to exhibit dominance behaviors. Furthermore, males METH self-administration was affected by dominance, with dominant males exhibiting greater responding for METH than non-dominant males. ConclusionsSocial housing provides some protective benefits to females, but not males, for METH self-administration. Further, the type of relationship between cage mates affects males self-administration and may explain why social housing with a same sex mate is not beneficial for males. HIGHLIGHTSO_LIPair housing in female rats resulted in less methamphetamine self-administration compared with individually housed females. C_LIO_LIPair housing in male rats did not attenuate methamphetamine self-administration compared with single housing. C_LIO_LIFemales self-administering methamphetamine spent more time together. C_LIO_LIMales self-administration of methamphetamine was affected by dominance status. C_LI

neuroscience↗

Sex Dependent Regional Differences in Dopamine Release Determined by Chronic Fast-Scan Cyclic Voltammetry in Nucleus Accumbens and Dorsal Striatum

We investigated sex differences in dopamine (DA) release in the nucleus accumbens (NAc) and dorsolateral striatum (DLS) using a chronic 16-channel carbon fiber electrode and fast-scan cyclic voltammetry (FSCV). Electrical stimulation (ES; 60Hz) induced DA release was recorded in the NAc of single or pair-housed male and female rats. When core (NAcC) and shell (NAcS) were recorded simultaneously, there was greater ES DA release in NAcC of pair-housed females compared with single females and males. Housing did not affect ES NAc DA release in males. In contrast, there was significantly more ES DA release from the DLS of female rats than male rats. This was true prior to and after treatment with methamphetamine. Furthermore, in castrated (CAST) males and ovariectomized (OVX) females, there were no sex differences in ES DA release from the DLS, demonstrating the hormone dependence of this sex difference. However, in the DLS of both intact and gonadectomized rats, DA reuptake was slower in females than in males. Finally, DA release following ES of the medial forebrain bundle at 60Hz was studied over four weeks. ES DA release increased over time for both CAST males and OVX females, demonstrating sensitization. Using this novel 16-channel chronic FSCV electrode, we found sex differences in the effects of social housing in the NAcS, sex differences in DA release from intact rats in DLS, sex differences in DA reuptake in DLS of intake and gonadectomized rats, and we report sensitization of ES-induced DA release in DLS in vivo. Significance StatementDopamine release is not uniform or fixed. In the nucleus accumbens, pair housing, compared with individual housing, is shown to differentially affect dopamine responsiveness to stimulation in a sex-dependent and region-specific way. There are also sex differences in stimulated dopamine release in the dorsolateral striatum of intact rats, which are not seen in gonadectomized rats, indicating the hormone dependence of this sex difference. However, reuptake of dopamine was slower in females than in males, independent of gonadal hormones. Importantly, the electrical stimulation-induced dopamine release in the dorsolateral striatum of gonadectomized rats demonstrated sensitization of dopamine release in vivo within animals for the first time. Thus, stimulated dopamine release exhibits sex-specific neuroplasticity that is modified in females by the housing conditions.

neuroscience↗