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The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals
AIM: Since GH stimulates lipolysis in vivo after a 2‐hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT). METHODS: Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene a...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029434/ https://www.ncbi.nlm.nih.gov/pubmed/32073221 http://dx.doi.org/10.14814/phy2.14373 |
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author | Høyer, Katrine L. Høgild, Morten L. List, Edward O. Lee, Kevin Y. Kissinger, Emily Sharma, Rita Erik Magnusson, Nils Puri, Vishwajeet Kopchick, John J. Jørgensen, Jens O. L. Jessen, Niels |
author_facet | Høyer, Katrine L. Høgild, Morten L. List, Edward O. Lee, Kevin Y. Kissinger, Emily Sharma, Rita Erik Magnusson, Nils Puri, Vishwajeet Kopchick, John J. Jørgensen, Jens O. L. Jessen, Niels |
author_sort | Høyer, Katrine L. |
collection | PubMed |
description | AIM: Since GH stimulates lipolysis in vivo after a 2‐hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT). METHODS: Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene array, and protein in AT biopsies after 30–120 min. Human data were corroborated in adipose‐specific GH receptor knockout (FaGHRKO) mice versus wild‐type mice. Expression of candidate genes identified in the array were investigated in 3T3‐L1 adipocytes. RESULTS: GH increased serum FFA and AT phosphorylation of STAT5b in human subjects. This was replicated in wild‐type mice, but not in FaGHRKO mice. The array identified 53 GH‐regulated genes, and Ingenuity Pathway analysis showed downregulation of PDE3b, an insulin‐dependent antilipolytic signal, upregulation of PTEN that inhibits insulin‐dependent antilipolysis, and downregulation of G0S2 and RASD1, both encoding antilipolytic proteins. This was confirmed in 3T3‐L1 adipocytes, except for PDE3B, including reciprocal effects of GH and insulin on mRNA expression of PTEN, RASD1, and G0S2. CONCLUSION: (a) GH directly stimulates AT lipolysis in a GHR‐dependent manner, (b) this involves suppression of antilipolytic signals at the level of gene expression, (c) the underlying GH signaling pathways remain to be defined. |
format | Online Article Text |
id | pubmed-7029434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70294342020-02-19 The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals Høyer, Katrine L. Høgild, Morten L. List, Edward O. Lee, Kevin Y. Kissinger, Emily Sharma, Rita Erik Magnusson, Nils Puri, Vishwajeet Kopchick, John J. Jørgensen, Jens O. L. Jessen, Niels Physiol Rep Original Research AIM: Since GH stimulates lipolysis in vivo after a 2‐hr lag phase, we studied whether this involves GH signaling and gene expression in adipose tissue (AT). METHODS: Human subjects (n = 9) each underwent intravenous exposure to GH versus saline with measurement of serum FFA, and GH signaling, gene array, and protein in AT biopsies after 30–120 min. Human data were corroborated in adipose‐specific GH receptor knockout (FaGHRKO) mice versus wild‐type mice. Expression of candidate genes identified in the array were investigated in 3T3‐L1 adipocytes. RESULTS: GH increased serum FFA and AT phosphorylation of STAT5b in human subjects. This was replicated in wild‐type mice, but not in FaGHRKO mice. The array identified 53 GH‐regulated genes, and Ingenuity Pathway analysis showed downregulation of PDE3b, an insulin‐dependent antilipolytic signal, upregulation of PTEN that inhibits insulin‐dependent antilipolysis, and downregulation of G0S2 and RASD1, both encoding antilipolytic proteins. This was confirmed in 3T3‐L1 adipocytes, except for PDE3B, including reciprocal effects of GH and insulin on mRNA expression of PTEN, RASD1, and G0S2. CONCLUSION: (a) GH directly stimulates AT lipolysis in a GHR‐dependent manner, (b) this involves suppression of antilipolytic signals at the level of gene expression, (c) the underlying GH signaling pathways remain to be defined. John Wiley and Sons Inc. 2020-02-19 /pmc/articles/PMC7029434/ /pubmed/32073221 http://dx.doi.org/10.14814/phy2.14373 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Høyer, Katrine L. Høgild, Morten L. List, Edward O. Lee, Kevin Y. Kissinger, Emily Sharma, Rita Erik Magnusson, Nils Puri, Vishwajeet Kopchick, John J. Jørgensen, Jens O. L. Jessen, Niels The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
title | The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
title_full | The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
title_fullStr | The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
title_full_unstemmed | The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
title_short | The acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
title_sort | acute effects of growth hormone in adipose tissue is associated with suppression of antilipolytic signals |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029434/ https://www.ncbi.nlm.nih.gov/pubmed/32073221 http://dx.doi.org/10.14814/phy2.14373 |
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