Bahareh Soltanahmadi , Mohammad Nasehi , Fatemeh Rohollah , Haniyeh Bashi Zadeh Fakhar , Soyar Sari
{"title":"The effects of crocin on fear condition memory impairment caused by morphine in relation to gene expression of amygdala HSP70, HSP90 and NF-kB","authors":"Bahareh Soltanahmadi , Mohammad Nasehi , Fatemeh Rohollah , Haniyeh Bashi Zadeh Fakhar , Soyar Sari","doi":"10.1016/j.genrep.2024.102108","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Some studies have shown that morphine causes memory impairment through different mechanisms. The roles of inflammation/NF-κB and BDNF/TrkB/CREB pathways are significant in the memory deficits caused by morphine. Aim: In this study, the effect of crocin on the impairment of fear memory caused by morphine was investigated, and the expression of HSP70, HSP90, and NF-kB genes that play an important role in memory in male Wistar rats was measured.</div></div><div><h3>Material and method</h3><div>The fear conditioning test was used to check the fear memory of rats, and total Freezing time was considered as an index of memory. Rats (96 Wistar rats) were randomly divided into 12 groups. The rats were injected with saline (1 ml/kg) or different doses of morphine (0.5, 2.5, and 5 mg/kg) 5 min after injection of saline (1 ml/kg) or subthreshold doses of crocin (60 mg/kg). Real-time PCR method was used for HSP70, HSP90, and NF-kB gene expression in the Amygdala.</div></div><div><h3>Result</h3><div>Administration of morphine 5 mg/kg decreased the total freezing and increased the latency freezing (P < 0.001). Also, the results showed that crocin 60 mg/kg reduced memory impairment induced by morphine. Real-time PCR analysis showed that morphine 5 mg/kg significantly increased the expression of the HSP70, HSP90, and NF-kB genes. However, the subthreshold dose of crocin (60 mg/kg) reduced the increase in gene expression.</div></div><div><h3>Conclusion</h3><div>The study showed that morphine impacts memory and boosts gene expression of HSP70, HSP90, and NF-kB, while crocin could potentially reverse this effect by regulating these amygdala genes, suggesting avenues for future research.</div></div>","PeriodicalId":12673,"journal":{"name":"Gene Reports","volume":"38 ","pages":"Article 102108"},"PeriodicalIF":1.0000,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gene Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452014424002310","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Some studies have shown that morphine causes memory impairment through different mechanisms. The roles of inflammation/NF-κB and BDNF/TrkB/CREB pathways are significant in the memory deficits caused by morphine. Aim: In this study, the effect of crocin on the impairment of fear memory caused by morphine was investigated, and the expression of HSP70, HSP90, and NF-kB genes that play an important role in memory in male Wistar rats was measured.
Material and method
The fear conditioning test was used to check the fear memory of rats, and total Freezing time was considered as an index of memory. Rats (96 Wistar rats) were randomly divided into 12 groups. The rats were injected with saline (1 ml/kg) or different doses of morphine (0.5, 2.5, and 5 mg/kg) 5 min after injection of saline (1 ml/kg) or subthreshold doses of crocin (60 mg/kg). Real-time PCR method was used for HSP70, HSP90, and NF-kB gene expression in the Amygdala.
Result
Administration of morphine 5 mg/kg decreased the total freezing and increased the latency freezing (P < 0.001). Also, the results showed that crocin 60 mg/kg reduced memory impairment induced by morphine. Real-time PCR analysis showed that morphine 5 mg/kg significantly increased the expression of the HSP70, HSP90, and NF-kB genes. However, the subthreshold dose of crocin (60 mg/kg) reduced the increase in gene expression.
Conclusion
The study showed that morphine impacts memory and boosts gene expression of HSP70, HSP90, and NF-kB, while crocin could potentially reverse this effect by regulating these amygdala genes, suggesting avenues for future research.
Gene ReportsBiochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.30
自引率
7.70%
发文量
246
审稿时长
49 days
期刊介绍:
Gene Reports publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses. Gene Reports strives to be a very diverse journal and topics in all fields will be considered for publication. Although not limited to the following, some general topics include: DNA Organization, Replication & Evolution -Focus on genomic DNA (chromosomal organization, comparative genomics, DNA replication, DNA repair, mobile DNA, mitochondrial DNA, chloroplast DNA). Expression & Function - Focus on functional RNAs (microRNAs, tRNAs, rRNAs, mRNA splicing, alternative polyadenylation) Regulation - Focus on processes that mediate gene-read out (epigenetics, chromatin, histone code, transcription, translation, protein degradation). Cell Signaling - Focus on mechanisms that control information flow into the nucleus to control gene expression (kinase and phosphatase pathways controlled by extra-cellular ligands, Wnt, Notch, TGFbeta/BMPs, FGFs, IGFs etc.) Profiling of gene expression and genetic variation - Focus on high throughput approaches (e.g., DeepSeq, ChIP-Seq, Affymetrix microarrays, proteomics) that define gene regulatory circuitry, molecular pathways and protein/protein networks. Genetics - Focus on development in model organisms (e.g., mouse, frog, fruit fly, worm), human genetic variation, population genetics, as well as agricultural and veterinary genetics. Molecular Pathology & Regenerative Medicine - Focus on the deregulation of molecular processes in human diseases and mechanisms supporting regeneration of tissues through pluripotent or multipotent stem cells.