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Entity

Name
Alcohol Drinking
Namespace
MeSH
Namespace Version
20181007
Namespace URL
https://raw.githubusercontent.com/pharmacome/terminology/c328ad964c08967a0417a887510b97b965a62fa5/external/mesh-names.belns

Appears in Networks 1

In-Edges 6

p(HGNC:ADNP, pmod(MESH:Haploinsufficiency)) increases path(MESH:"Alcohol Drinking") View Subject | View Object

Importantly, Adnp+/− females showed higher alcohol consumption and preference, compared to female Adnp+/+ controls, whereas no difference was observed in males. PubMed:30008470

p(HGNC:ADNP, pmod(MESH:Haploinsufficiency)) causesNoChange path(MESH:"Alcohol Drinking") View Subject | View Object

Importantly, Adnp+/− females showed higher alcohol consumption and preference, compared to female Adnp+/+ controls, whereas no difference was observed in males. PubMed:30008470

p(HGNC:ADNP, pmod(MESH:Haploinsufficiency)) increases path(MESH:"Alcohol Drinking") View Subject | View Object

As shown in Fig. 3e, f, we found no difference between genotypes in saccharin or quinine intake, suggesting that the effect of Adnp deficiency is specific to alcohol, and does not apply to sweet reinforcers or bitter-taste solutions PubMed:30008470

p(HGNC:ADNP, pmod(MESH:Haploinsufficiency)) increases path(MESH:"Alcohol Drinking") View Subject | View Object

As Fig. 4b depicts, over the first 2 weeks of drinking (no treatment or intranasal vehicle treatment) Adnp+/− females showed higher alcohol consumption as compared to their Adnp+/+ littermates, replicating our results above. PubMed:30008470

g(HGNC:ADNP) negativeCorrelation path(MESH:"Alcohol Drinking") View Subject | View Object

Together, our results indicate that reduced Adnp gene dosage leads to increased alcohol intake in female mice. PubMed:30008470

Out-Edges 9

path(MESH:"Alcohol Drinking") increases p(HGNC:ADNP) View Subject | View Object

In addition, Adnp expression was increased at the 24 h time point in the NAc of female, but not male mouse (one-way ANOVA; females: F(2,9) = 10.87, p < 0.005; post hoc: p < 0.005; males: p > 0.05). PubMed:30008470

path(MESH:"Alcohol Drinking") increases r(HGNC:ADNP) View Subject | View Object

As shown in Fig. 1, we found that this sub-chronic alcohol treatment increased Adnp mRNA levels in the dorsal hippocampus 24 h, but not 2 h after the last alcohol injection, in both male and female mice (one-way ANOVA; males: F(2,10) = 5.94, p < 0.05; post-hoc, p < 0.02. Females: F(2,10) = 5.22, p < 0.05, post hoc, p < 0.05) PubMed:30008470

path(MESH:"Alcohol Drinking") causesNoChange p(HGNC:ADNP) View Subject | View Object

In addition, Adnp expression was increased at the 24 h time point in the NAc of female, but not male mouse (one-way ANOVA; females: F(2,9) = 10.87, p < 0.005; post hoc: p < 0.005; males: p > 0.05). PubMed:30008470

path(MESH:"Alcohol Drinking") increases p(HGNC:ADNP) View Subject | View Object

We found that among male mice, Adnp mRNA levels were increased in the dorsal hippocampus after a 24 h alcohol drinking session, but the level returned to baseline (water-drinking controls) after 24 h of withdrawal (Fig. 2b; one-way ANOVA: F(2,13) = 5.32, p < 0.05, post hoc comparisons, p’s < 0.05) PubMed:30008470

path(MESH:"Alcohol Drinking") decreases p(HGNC:ADNP) View Subject | View Object

However, in female mice, the expression of Adnp was reduced after a 24-h alcohol-drinking session, and this reduction persisted after a 24-h withdrawal (Fig. 2c; one-way ANOVA: F(2,13) = 7.53, p < 0.01, post hoc comparisons, p’s < 0.05). PubMed:30008470

path(MESH:"Alcohol Drinking") negativeCorrelation g(HGNC:ADNP) View Subject | View Object

Together, our results indicate that reduced Adnp gene dosage leads to increased alcohol intake in female mice. PubMed:30008470

path(MESH:"Alcohol Drinking") decreases p(HGNC:TFAP2B) View Subject | View Object

For example, one of these common genes was transcription factor AP2 beta (TFAP2b), which is downregulated by chronic alcohol exposure [41]. This gene had a 3.8-fold increased expression in female Adnp+/− mice, and in contrast, a five-fold decreased expression in male Adnp+/− mice, as compared to sex-matched Adnp+/+controls. PubMed:30008470

About

BEL Commons is developed and maintained in an academic capacity by Charles Tapley Hoyt and Daniel Domingo-Fernández at the Fraunhofer SCAI Department of Bioinformatics with support from the IMI project, AETIONOMY. It is built on top of PyBEL, an open source project. Please feel free to contact us here to give us feedback or report any issues. Also, see our Publishing Notes and Data Protection information.

If you find BEL Commons useful in your work, please consider citing: Hoyt, C. T., Domingo-Fernández, D., & Hofmann-Apitius, M. (2018). BEL Commons: an environment for exploration and analysis of networks encoded in Biological Expression Language. Database, 2018(3), 1–11.