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Mimicking chronic alcohol effects through a controlled and sustained ethanol release device
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Wanil | - |
| dc.contributor.author | Chu, Jin-Ok | - |
| dc.contributor.author | Kim, Do-Yeon | - |
| dc.contributor.author | Lee, Soo-Hyeon | - |
| dc.contributor.author | Choi, Chang-Hyung | - |
| dc.contributor.author | Lee, Kyung-Ha | - |
| dc.date.accessioned | 2024-05-21T07:00:16Z | - |
| dc.date.available | 2024-05-21T07:00:16Z | - |
| dc.date.issued | 2024-05 | - |
| dc.identifier.issn | 1754-1611 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/70600 | - |
| dc.description.abstract | Alcohol consumption, a pervasive societal issue, poses considerable health risks and socioeconomic consequences. Alcohol-induced hepatic disorders, such as fatty liver disease, alcoholic hepatitis, chronic hepatitis, liver fibrosis, and cirrhosis, underscore the need for comprehensive research. Existing challenges in mimicking chronic alcohol exposure in cellular systems, attributed to ethanol evaporation, necessitate innovative approaches. In this study, we developed a simple, reusable, and controllable device for examining the physiological reactions of hepatocytes to long-term alcohol exposure. Our approach involved a novel device designed to continuously release ethanol into the culture medium, maintaining a consistent ethanol concentration over several days. We evaluated device performance by examining gene expression patterns and cytokine secretion alterations during long-term exposure to ethanol. These patterns were correlated with those observed in patients with alcoholic hepatitis. Our results suggest that our ethanol-releasing device can be used as a valuable tool to study the mechanisms of chronic alcohol-mediated hepatic diseases at the cellular level. Our device offers a practical solution for studying chronic alcohol exposure, providing a reliable platform for cellular research. This innovative tool holds promise for advancing our understanding of the molecular processes involved in chronic alcohol-mediated hepatic diseases. Future research avenues should explore broader applications and potential implications for predicting and treating alcohol-related illnesses. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | BioMed Central | - |
| dc.title | Mimicking chronic alcohol effects through a controlled and sustained ethanol release device | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1186/s13036-024-00428-1 | - |
| dc.identifier.scopusid | 2-s2.0-85192360635 | - |
| dc.identifier.wosid | 001215615000002 | - |
| dc.identifier.bibliographicCitation | Journal of Biological Engineering, v.18, no.1 | - |
| dc.citation.title | Journal of Biological Engineering | - |
| dc.citation.volume | 18 | - |
| dc.citation.number | 1 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalResearchArea | Biotechnology & Applied Microbiology | - |
| dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
| dc.relation.journalWebOfScienceCategory | Biotechnology & Applied Microbiology | - |
| dc.subject.keywordPlus | LIVER-DISEASE | - |
| dc.subject.keywordPlus | CC-CHEMOKINE | - |
| dc.subject.keywordPlus | IN-VITRO | - |
| dc.subject.keywordPlus | RECEPTOR | - |
| dc.subject.keywordPlus | ANGIOGENESIS | - |
| dc.subject.keywordPlus | PATHOGENESIS | - |
| dc.subject.keywordPlus | ACTIVATION | - |
| dc.subject.keywordPlus | EXPRESSION | - |
| dc.subject.keywordPlus | CYTOKINES | - |
| dc.subject.keywordPlus | BURDEN | - |
| dc.subject.keywordAuthor | Ethanol | - |
| dc.subject.keywordAuthor | Ethanol-releasing device | - |
| dc.subject.keywordAuthor | Polydimethylsiloxane | - |
| dc.subject.keywordAuthor | Alcohol | - |
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