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Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles

BACKGROUND: Fat storage is required for the life cycle of many organisms. The primary fat depot for most vertebrates is white adipose tissue. However, in primitive vertebrates (e.g., agnathan group and elasmobranchs), the liver is usually responsible for fat storage. Among the vertebrates, amphibian...

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Autores principales: Zhu, Wei, Zhang, Meihua, Chang, Liming, Zhu, Wenbo, Li, Cheng, Xie, Feng, Zhang, Huan, Zhao, Tian, Jiang, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854647/
https://www.ncbi.nlm.nih.gov/pubmed/31754367
http://dx.doi.org/10.1186/s12983-019-0341-x
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author Zhu, Wei
Zhang, Meihua
Chang, Liming
Zhu, Wenbo
Li, Cheng
Xie, Feng
Zhang, Huan
Zhao, Tian
Jiang, Jianping
author_facet Zhu, Wei
Zhang, Meihua
Chang, Liming
Zhu, Wenbo
Li, Cheng
Xie, Feng
Zhang, Huan
Zhao, Tian
Jiang, Jianping
author_sort Zhu, Wei
collection PubMed
description BACKGROUND: Fat storage is required for the life cycle of many organisms. The primary fat depot for most vertebrates is white adipose tissue. However, in primitive vertebrates (e.g., agnathan group and elasmobranchs), the liver is usually responsible for fat storage. Among the vertebrates, amphibians have a unique status, as their larvae live in the water and exhibit some primitive traits that are similar to fish. Although it has been recognized that adult frogs use their abdominal white adipose tissue as a primary fat depot, how tadpoles store their fat is still inconclusive. The metabolic traits and physiological functions of primitive fat depots may have wide-ranging implications on the pathology of abnormal lipid deposition in mammals and the evolution of fat storage. RESULTS: Rana omeimontis tadpoles used their liver as the primary fat depot. In sufficiently fed tadpoles at stage 30–31, the hepatosomatic index (HSI) reached up to 7%, and triglycerides (TG) accounted for 15% of liver weight. Their liver resembled white adipose tissue in histological morphology, characterized by polygonal hepatocytes filled with fat. Their liver metabolic composition was unique, characterized by the dominance of maltotriose, arachidonic acid and dipeptides in soluble carbohydrates, free fatty acids and amino acids. Hepatic fat was the major metabolic fuel of fasted R. omeimontis tadpoles, which had similar reserve mobilization and allocation patterns as mammals. From a developmental perspective, hepatic fat was important to fuel late metamorphic climax. Interestingly, starvation induced accelerated metamorphosis in tadpoles with high HSI (4.96 ± 0.21%). However, this phenomenon was not observed in tadpoles with low HSI (2.71 ± 0.16%), even though they had similar initial body weight and developmental stage. Hepatic fat abundance was the most prominent difference between the two groups. CONCLUSION: To the best of our knowledge, this is the first report that liver can be the primary fat depot in vertebrates with higher evolutionary status than bony fish. The unique hepatic histological and metabolic traits likely either guard their liver against lipotoxicity or make their hepatocytes adapt to fat accumulation. This fatty liver could be a primitive counterpart of mammalian white adipose tissue (WAT). In addition, our study showed that the hepatic reserves of tadpoles, especially TG content, may provide body condition signals to modulate metamorphosis.
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spelling pubmed-68546472019-11-21 Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles Zhu, Wei Zhang, Meihua Chang, Liming Zhu, Wenbo Li, Cheng Xie, Feng Zhang, Huan Zhao, Tian Jiang, Jianping Front Zool Research BACKGROUND: Fat storage is required for the life cycle of many organisms. The primary fat depot for most vertebrates is white adipose tissue. However, in primitive vertebrates (e.g., agnathan group and elasmobranchs), the liver is usually responsible for fat storage. Among the vertebrates, amphibians have a unique status, as their larvae live in the water and exhibit some primitive traits that are similar to fish. Although it has been recognized that adult frogs use their abdominal white adipose tissue as a primary fat depot, how tadpoles store their fat is still inconclusive. The metabolic traits and physiological functions of primitive fat depots may have wide-ranging implications on the pathology of abnormal lipid deposition in mammals and the evolution of fat storage. RESULTS: Rana omeimontis tadpoles used their liver as the primary fat depot. In sufficiently fed tadpoles at stage 30–31, the hepatosomatic index (HSI) reached up to 7%, and triglycerides (TG) accounted for 15% of liver weight. Their liver resembled white adipose tissue in histological morphology, characterized by polygonal hepatocytes filled with fat. Their liver metabolic composition was unique, characterized by the dominance of maltotriose, arachidonic acid and dipeptides in soluble carbohydrates, free fatty acids and amino acids. Hepatic fat was the major metabolic fuel of fasted R. omeimontis tadpoles, which had similar reserve mobilization and allocation patterns as mammals. From a developmental perspective, hepatic fat was important to fuel late metamorphic climax. Interestingly, starvation induced accelerated metamorphosis in tadpoles with high HSI (4.96 ± 0.21%). However, this phenomenon was not observed in tadpoles with low HSI (2.71 ± 0.16%), even though they had similar initial body weight and developmental stage. Hepatic fat abundance was the most prominent difference between the two groups. CONCLUSION: To the best of our knowledge, this is the first report that liver can be the primary fat depot in vertebrates with higher evolutionary status than bony fish. The unique hepatic histological and metabolic traits likely either guard their liver against lipotoxicity or make their hepatocytes adapt to fat accumulation. This fatty liver could be a primitive counterpart of mammalian white adipose tissue (WAT). In addition, our study showed that the hepatic reserves of tadpoles, especially TG content, may provide body condition signals to modulate metamorphosis. BioMed Central 2019-11-14 /pmc/articles/PMC6854647/ /pubmed/31754367 http://dx.doi.org/10.1186/s12983-019-0341-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhu, Wei
Zhang, Meihua
Chang, Liming
Zhu, Wenbo
Li, Cheng
Xie, Feng
Zhang, Huan
Zhao, Tian
Jiang, Jianping
Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles
title Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles
title_full Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles
title_fullStr Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles
title_full_unstemmed Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles
title_short Characterizing the composition, metabolism and physiological functions of the fatty liver in Rana omeimontis tadpoles
title_sort characterizing the composition, metabolism and physiological functions of the fatty liver in rana omeimontis tadpoles
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854647/
https://www.ncbi.nlm.nih.gov/pubmed/31754367
http://dx.doi.org/10.1186/s12983-019-0341-x
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