{"title":"急性缺氧导致糖酵解和脂质代谢改变,HSPs持续活化长尾鲤","authors":"","doi":"10.1007/s10228-024-00954-4","DOIUrl":null,"url":null,"abstract":"<h3>Abstract</h3> <p>Hypoxia is one of the common stress factors encountered in intensive farming. <em>Leiocassis longirostris</em> is a commercially valuable fish with limited information on the response mechanism under acute hypoxia stress. Here, we detected the asphyxiation point and simulated acute hypoxia conditions, dissolved oxygen decreased, hypoxia maintained, and reoxygenation, and investigated molecular changes in the liver of <em>L. longirostris</em>. Results showed that the hypoxia-inducible factor-1 signaling pathway was enriched and <em>hif1α</em>, <em>arnt</em>, <em>hph</em>, <em>epo</em>, <em>epor</em>, and <em>glut1</em> gene expression significantly increased. Peroxisome proliferator-activated receptor pathway with lipid metabolism-related genes (<em>gk</em>, <em>scd</em>, <em>acsl</em>, <em>pgar</em>, <em>lpl</em>, <em>fabp3</em>) was inhibited, while the glycolysis pathway with its related genes (<em>pk</em>, <em>gapdhs</em>, <em>ldh</em>, <em>pfk</em>, <em>aldo</em>, <em>hk</em>, <em>gpi</em>, <em>pfkfb3</em>) was activated under hypoxia. Furthermore, heat shock protein family gene expression increased significantly in both hypoxia treatments and the reoxygenation group, which suggests that immune response persistent activation was induced by acute hypoxic stress. This study provided valuable information for the metabolism and immune response in <em>L. longirostris</em> liver under acute hypoxia and reoxygenation conditions.</p>","PeriodicalId":13237,"journal":{"name":"Ichthyological Research","volume":"40 1","pages":""},"PeriodicalIF":0.6000,"publicationDate":"2024-02-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Acute hypoxia causes glycolysis and lipid metabolism alterations with HSPs’ persistent activation in Leiocassis longirostris\",\"authors\":\"\",\"doi\":\"10.1007/s10228-024-00954-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<h3>Abstract</h3> <p>Hypoxia is one of the common stress factors encountered in intensive farming. <em>Leiocassis longirostris</em> is a commercially valuable fish with limited information on the response mechanism under acute hypoxia stress. Here, we detected the asphyxiation point and simulated acute hypoxia conditions, dissolved oxygen decreased, hypoxia maintained, and reoxygenation, and investigated molecular changes in the liver of <em>L. longirostris</em>. Results showed that the hypoxia-inducible factor-1 signaling pathway was enriched and <em>hif1α</em>, <em>arnt</em>, <em>hph</em>, <em>epo</em>, <em>epor</em>, and <em>glut1</em> gene expression significantly increased. Peroxisome proliferator-activated receptor pathway with lipid metabolism-related genes (<em>gk</em>, <em>scd</em>, <em>acsl</em>, <em>pgar</em>, <em>lpl</em>, <em>fabp3</em>) was inhibited, while the glycolysis pathway with its related genes (<em>pk</em>, <em>gapdhs</em>, <em>ldh</em>, <em>pfk</em>, <em>aldo</em>, <em>hk</em>, <em>gpi</em>, <em>pfkfb3</em>) was activated under hypoxia. Furthermore, heat shock protein family gene expression increased significantly in both hypoxia treatments and the reoxygenation group, which suggests that immune response persistent activation was induced by acute hypoxic stress. This study provided valuable information for the metabolism and immune response in <em>L. longirostris</em> liver under acute hypoxia and reoxygenation conditions.</p>\",\"PeriodicalId\":13237,\"journal\":{\"name\":\"Ichthyological Research\",\"volume\":\"40 1\",\"pages\":\"\"},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2024-02-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ichthyological Research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s10228-024-00954-4\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"FISHERIES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ichthyological Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10228-024-00954-4","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"FISHERIES","Score":null,"Total":0}
Acute hypoxia causes glycolysis and lipid metabolism alterations with HSPs’ persistent activation in Leiocassis longirostris
Abstract
Hypoxia is one of the common stress factors encountered in intensive farming. Leiocassis longirostris is a commercially valuable fish with limited information on the response mechanism under acute hypoxia stress. Here, we detected the asphyxiation point and simulated acute hypoxia conditions, dissolved oxygen decreased, hypoxia maintained, and reoxygenation, and investigated molecular changes in the liver of L. longirostris. Results showed that the hypoxia-inducible factor-1 signaling pathway was enriched and hif1α, arnt, hph, epo, epor, and glut1 gene expression significantly increased. Peroxisome proliferator-activated receptor pathway with lipid metabolism-related genes (gk, scd, acsl, pgar, lpl, fabp3) was inhibited, while the glycolysis pathway with its related genes (pk, gapdhs, ldh, pfk, aldo, hk, gpi, pfkfb3) was activated under hypoxia. Furthermore, heat shock protein family gene expression increased significantly in both hypoxia treatments and the reoxygenation group, which suggests that immune response persistent activation was induced by acute hypoxic stress. This study provided valuable information for the metabolism and immune response in L. longirostris liver under acute hypoxia and reoxygenation conditions.
期刊介绍:
Ichthyological Research is an official journal of the Ichthyological Society of Japan and is published quarterly in January, April, July, and November. Ichthyological Research primarily publishes research papers on original work, either descriptive or experimental, that advances the understanding of the diversity of fishes. Ichthyological Research strives to cover all aspects of fish biology, including taxonomy, systematics, evolution, biogeography, ecology, ethology, genetics, morphology, and physiology.