Combined Addiction and Neurobiological Targets: An In Silico Analysis of Areca Nut and Areca Nut with Tobacco Biomolecules.

Q3 Pharmacology, Toxicology and Pharmaceutics Neuropsychopharmacologia Hungarica Pub Date : 2024-09-01
Anusa Arunachalam Mohandoss, Rooban Thavarajah
{"title":"Combined Addiction and Neurobiological Targets: An In Silico Analysis of Areca Nut and Areca Nut with Tobacco Biomolecules.","authors":"Anusa Arunachalam Mohandoss, Rooban Thavarajah","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The addictive potential of areca nut (AN) and tobacco is well-documented, but their combined neurobiological effects in AN-containing tobacco products (ANTP) remain obscure. This study employed a three-stage in silico approach to investigate the potential targets and pathways associated with the addictive properties of AN alone and in ANTP.</p><p><strong>Materials and methods: </strong>Bioactive molecules were retrieved for AN and tobacco, followed by target prediction and pathway enrichment analysis. The identified biomolecules were categorized into AN and ANTP groups.</p><p><strong>Results: </strong>A total of 195 bioactive molecules were identifid (38 to AN, 157 to tobacco). Absorption, distribution, metabolism, and excretion (ADME) details were retrieved. Predicted bioactivity (gene/protein interaction probability ≥80%) was analysed, revealing 13 shared targets between AN and tobacco, 12 exclusive to AN, and 33 exclusive to tobacco. AN and ANTP influenced 21 and 27 pathways (FDR ≤ 0.05), respectively, with distinct footprints. Notably, GABAergic and cholinergic synapses, nicotine addiction, calcium signaling, and morphine addiction pathways were differentially enriched between AN and ANTP.</p><p><strong>Discussion: </strong>This study highlights the distinct and synergistic neurobiological effects of AN and tobacco in ANTP. The identified differences in target genes and pathways underscore the need for tailored interventions and cessation strategies for users of AN and ANTP products. Further research is warranted to validate these findings, explore interplay between diverse addiction factors, and develop effective prevention and treatment programs. \n(Neuropsychopharmacol Hung 2024; 26(3): 133-143)</p>","PeriodicalId":39762,"journal":{"name":"Neuropsychopharmacologia Hungarica","volume":"26 3","pages":"133-143"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuropsychopharmacologia Hungarica","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The addictive potential of areca nut (AN) and tobacco is well-documented, but their combined neurobiological effects in AN-containing tobacco products (ANTP) remain obscure. This study employed a three-stage in silico approach to investigate the potential targets and pathways associated with the addictive properties of AN alone and in ANTP.

Materials and methods: Bioactive molecules were retrieved for AN and tobacco, followed by target prediction and pathway enrichment analysis. The identified biomolecules were categorized into AN and ANTP groups.

Results: A total of 195 bioactive molecules were identifid (38 to AN, 157 to tobacco). Absorption, distribution, metabolism, and excretion (ADME) details were retrieved. Predicted bioactivity (gene/protein interaction probability ≥80%) was analysed, revealing 13 shared targets between AN and tobacco, 12 exclusive to AN, and 33 exclusive to tobacco. AN and ANTP influenced 21 and 27 pathways (FDR ≤ 0.05), respectively, with distinct footprints. Notably, GABAergic and cholinergic synapses, nicotine addiction, calcium signaling, and morphine addiction pathways were differentially enriched between AN and ANTP.

Discussion: This study highlights the distinct and synergistic neurobiological effects of AN and tobacco in ANTP. The identified differences in target genes and pathways underscore the need for tailored interventions and cessation strategies for users of AN and ANTP products. Further research is warranted to validate these findings, explore interplay between diverse addiction factors, and develop effective prevention and treatment programs. (Neuropsychopharmacol Hung 2024; 26(3): 133-143)

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
成瘾与神经生物学目标的结合:阿雷卡果和阿雷卡果与烟草生物分子的硅学分析。
背景:槟榔(AN)和烟草的成瘾潜力已得到充分证实,但它们在含槟榔烟草制品(ANTP)中的综合神经生物学效应仍不明显。本研究采用了三阶段的硅学方法来研究与单独的 AN 和 ANTP 上瘾特性相关的潜在靶点和途径:检索了苯丙胺和烟草的生物活性分子,然后进行了靶点预测和通路富集分析。结果:共发现 195 个生物活性分子:结果:共鉴定出 195 个生物活性分子(38 个属于 AN 组,157 个属于烟草组)。检索了吸收、分布、代谢和排泄(ADME)的详细信息。对预测的生物活性(基因/蛋白质相互作用概率≥80%)进行了分析,结果显示 AN 和烟草之间有 13 个共享靶点,12 个为 AN 独有靶点,33 个为烟草独有靶点。AN 和 ANTP 分别影响了 21 条和 27 条通路(FDR ≤ 0.05),它们的足迹各不相同。值得注意的是,GABA能和胆碱能突触、尼古丁成瘾、钙信号转导和吗啡成瘾通路在AN和ANTP之间的富集程度不同:本研究强调了 ANTP 和烟草对神经生物学的不同协同作用。已确定的靶基因和通路的差异突出表明,有必要为AN和ANTP产品的使用者制定有针对性的干预措施和戒烟策略。为了验证这些发现、探索不同成瘾因素之间的相互作用以及制定有效的预防和治疗方案,我们有必要开展进一步的研究。(Neuropsychopharmacol Hung 2024; 26(3):133-143)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Neuropsychopharmacologia Hungarica
Neuropsychopharmacologia Hungarica Medicine-Medicine (all)
CiteScore
1.60
自引率
0.00%
发文量
8
期刊最新文献
[Clinical Pathway for Suicide Risk Screening in Adult Primary Care Settings:Special Recommendations]. [Summarising the efficiency of psychological interventions in the treatment of endometriosis]. Assessing obsessive-compulsive symptoms in a subclinical and clinical sample: the development of the Hungarian version of the OCI-R. Combined Addiction and Neurobiological Targets: An In Silico Analysis of Areca Nut and Areca Nut with Tobacco Biomolecules. The Implications of Sanctions on Civilian Mental Health and Quality of life Iranian: An overview.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1