Browsing by Author "Melón, Laverne C."

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    Activation of extrasynaptic δ-GABAA receptors globally or within the posterior-VTA has estrous-dependent effects on consumption of alcohol and estrous-independent effects on locomotion
    (Elsevier, 2017-09) Melón, Laverne C.; Nolan, Zachary T.; Colar, Delphine; Moore, Eileen M.; Boehm II, Stephen L.; Psychology, School of Science
    Recent reports support higher than expected rates of binge alcohol consumption among women and girls. Unfortunately, few studies have assessed the mechanisms underlying this pattern of intake in females. Studies in males suggest that alcohol concentrations relevant to the beginning stages of binge intoxication may selectively target tonic GABAergic inhibition mediated by GABAA receptor subtypes expressing the δ-subunit protein (δ-GABAARs). Indeed, administration of agonists that interact with these δ-GABAARs prior to alcohol access can abolish binge drinking behavior in male mice. These δ-GABAARs have also been shown to exhibit estrous-dependent plasticity in regions relevant to drug taking behavior, like the hippocampus and periaqueductal gray. The present experiments were designed to determine whether the estrous cycle would alter binge drinking, or our ability to modulate this pattern of alcohol use with THIP, an agonist with high selectivity and efficacy at δ-GABAARs. Using the Drinking-in-the-Dark (DID) binge-drinking model, regularly cycling female mice were given 2h of daily access to alcohol (20%v/v). Vaginal cytology or vaginal impedance was assessed after drinking sessions to track estrous status. There was no fluctuation in binge drinking associated with the estrous cycle. Both Intra-posterior-VTA administration of THIP and systemic administration of the drug was also associated with an estrous cycle dependent reduction in drinking behavior. Pre-treatment with finasteride to inhibit synthesis of 5α-reduced neurosteroids did not disrupt THIP's effects. Analysis of δ-subunit mRNA from posterior-VTA enriched tissue samples revealed that expression of this GABAA receptor subunit is elevated during diestrus in this region. Taken together, these studies demonstrate that δGABAARs in the VTA are an important target for binge drinking in females and confirm that the estrous cycle is an important moderator of the pharmacology of this GABAA receptor subtype.
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    ACTIVATION OF GABAA RECEPTORS AND INHIBITION OF NEUROSTEROID SYNTHESIS HAVE SEPARABLE ESTROUS-DEPENDENT EFFECTS ON BINGE DRINKING IN FEMALE MICE
    (Office of the Vice Chancellor for Research, 2012-04-13) Melón, Laverne C.; Nolan, Zachary T.; Boehm, Stephen L.
    Alcohol concentrations relevant to the beginning stages of binge intoxica-tion may selectively activate GABAA receptor subtypes expressing δ-subunit proteins (δ-GABAAR). Indeed, administration of agonists that interact with these δ-GABAAR prior to alcohol access, can abolish binge drinking behavior (Melon and Boehm, 2011). Unfortunately, our ability to manipulate binge drinking in females is dependent upon estrous phase. The present experi-ments were designed to clarify the estrous-dependent effects of activation of δ-GABAAR on binge drinking. Specifically, we were interested in demonstrat-ing whether females display more persistent binge drinking as a function of cycle-dependent changes in the synthesis of endogenous neurosteroids that modulate δ-GABAAR. Using the Drinking-in-the-Dark binge-drinking model, regularly cycling female mice were given 2 hours of daily access to alcohol (20%v/v). Vaginal cytology was assessed after each drinking session to track estrous status. In experiment 1, animals were administered gaboxadol (an agonist with high affinity for δ-GABAAR) prior to their 8th day of access. In experiment 2, these methods were repeated, but mice received vehicle or finasteride (a neurosteroid synthesis inhibitor) 22hr prior to their 8th day of access. Results from experiment 1 demonstrated that diestrus females were insensitive to the significant gaboxadol-induced decrease in binge drinking observed for proestrus, estrus and metestrus females. In experiment 2, ve-hicle and finasteride treated diestrus females exhibited gaboxadol-induced reduction of their binge drinking. Surprisingly, finasteride pretreatment sig-nificantly reduced binge drinking for estrus females. These studies suggest that ovarian-linked changes to extrasynaptic GABAA R and to neurosteroid activity may be important factors in the binge consumption of alcohol for females. Future studies will further explore the role that acute stress during diestrus may play in inhibiting the effects of δ-GABAA R activation on binge drinking.
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    Sex and age differences in heavy binge drinking and its effects on alcohol responsivity following abstinence
    (Elsevier, 2013) Melón, Laverne C.; Wray, Kevin N.; Moore, Eileen M.; Boehm, Stephen L., II; Psychology, School of Science
    Binge drinking during adolescence may perturb the maturing neuroenvironment and increase susceptibility of developing an alcohol use disorder later in life. In the present series of experiments, we utilized a modified version of the drinking in the dark-multiple scheduled access (DID-MSA) procedure to study how heavy binge drinking during adolescence alters responsivity to ethanol later in adulthood. Adult and adolescent C57BL/6J (B6) and DBA/2J (D2) males and females were given access to a 20% ethanol solution for 3 hourly periods, each separated by 2h of free water access. B6 adults and adolescents consumed 2 to 3.5 g/kg ethanol an hour and displayed significant intoxication and binge-like blood ethanol concentrations. There was an interaction of sex and age, however, driven by high intakes in adult B6 females, who peaked at 11.01 g/kg. Adolescents of both sexes and adult males never consumed more than 9.3 g/kg. D2 mice consumed negligible amounts of alcohol and showed no evidence of intoxication. B6 mice were abstinent for one month and were retested on the balance beam 10 min following 1.75 g/kg ethanol challenge (20%v/v; i.p). They were also tested for changes in home cage locomotion immediately following the 1.75 g/kg dose (for 10 min prior to balance beam). Although there was no effect of age of exposure, all mice with a binge drinking history demonstrated a significantly dampened ataxic response to an ethanol challenge. Female mice that binge drank during adulthood showed a significantly augmented locomotor response to ethanol when compared to their water drinking controls. This alteration was not noted for males or for females that binge drank during adolescence. These results highlight the importance of biological sex, and its interaction with age, in the development of behavioral adaptation following binge drinking.