Oleksandra Yu Kushnir, Iryna M Yaremii, Kyrylo A Pantsiuk, Oleksandra O Kushnir, Kateryna M Yaremii, Kateryna V Vlasova, Olena V Vlasova
{"title":"Carbohydrate metabolism in the rats' liver under conditions of light and dark deprivation and correction by melatonin.","authors":"Oleksandra Yu Kushnir, Iryna M Yaremii, Kyrylo A Pantsiuk, Oleksandra O Kushnir, Kateryna M Yaremii, Kateryna V Vlasova, Olena V Vlasova","doi":"10.36740/WLek/205592","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Aim: This study aimed to investigate changes in carbohydrate metabolism in the liver of rats under light and dark deprivation and evaluate the effects of melatonin treatment.</p><p><strong>Patients and methods: </strong>Materials and Methods: Photoperiodic changes were simulated over two weeks: the natural equinox (March 16-29); the artificial equinox (12:12 light-dark cycle, 500 lux); constant light (24 hours, 500 lux) for dark deprivation; and constant dark (24 hours, 0-0.5 lux) for light deprivation. Forty-eight rats were divided into control and melatonin-treated groups (5 mg/kg daily for 14 days). Enzyme activities and glycogen content in the liver were measured using standard methods. Statistical analysis was performed using the Student's t-test.</p><p><strong>Results: </strong>Results: Glucose-6-phosphate dehydrogenase activity decreased by 18% under constant light but increased by 35% under constant dark compared to the equinox. Pyruvate kinase activity decreased by 17%, while glucose-6-phosphatase and lactate dehydrogenase activities increased by 9% and 20%, respectively, under constant light. Constant dark and melatonin treatment reduced glucose levels by 26% across all conditions, activated aerobic pathways, and increased glycogen content by 13% compared to the equinox.</p><p><strong>Conclusion: </strong>Conclusions: Melatonin treatment improved carbohydrate metabolism in the liver of rats under light and dark deprivation, suggesting its role in metabolic adaptation to altered photoperiods.</p>","PeriodicalId":23643,"journal":{"name":"Wiadomosci lekarskie","volume":"78 7","pages":"1361-1366"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Wiadomosci lekarskie","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36740/WLek/205592","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Aim: This study aimed to investigate changes in carbohydrate metabolism in the liver of rats under light and dark deprivation and evaluate the effects of melatonin treatment.
Patients and methods: Materials and Methods: Photoperiodic changes were simulated over two weeks: the natural equinox (March 16-29); the artificial equinox (12:12 light-dark cycle, 500 lux); constant light (24 hours, 500 lux) for dark deprivation; and constant dark (24 hours, 0-0.5 lux) for light deprivation. Forty-eight rats were divided into control and melatonin-treated groups (5 mg/kg daily for 14 days). Enzyme activities and glycogen content in the liver were measured using standard methods. Statistical analysis was performed using the Student's t-test.
Results: Results: Glucose-6-phosphate dehydrogenase activity decreased by 18% under constant light but increased by 35% under constant dark compared to the equinox. Pyruvate kinase activity decreased by 17%, while glucose-6-phosphatase and lactate dehydrogenase activities increased by 9% and 20%, respectively, under constant light. Constant dark and melatonin treatment reduced glucose levels by 26% across all conditions, activated aerobic pathways, and increased glycogen content by 13% compared to the equinox.
Conclusion: Conclusions: Melatonin treatment improved carbohydrate metabolism in the liver of rats under light and dark deprivation, suggesting its role in metabolic adaptation to altered photoperiods.