File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.metabol.2018.06.007
- Scopus: eid_2-s2.0-85050402133
- PMID: 29935237
- WOS: WOS:000454746800015
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: BDNF mimetic alleviates body weight gain in obese mice by enhancing mitochondrial biogenesis in skeletal muscle
Title | BDNF mimetic alleviates body weight gain in obese mice by enhancing mitochondrial biogenesis in skeletal muscle |
---|---|
Authors | |
Keywords | 7,8-Dihydroxyflavone Mitochondrial Obesity Skeletal muscle |
Issue Date | 2018 |
Publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/metabol |
Citation | Metabolism, 2018, v. 87, p. 113-122 How to Cite? |
Abstract | Background: 7,8-Dihydroxyflavone (7,8-DHF) is a small molecular weight compound that mimics the functions of brain-derived neurotrophic factor (BDNF). The current study aims to elucidate the molecular mechanism of 7,8-DHF-induced body weight regulation. Methods: Obese female C57/BL6 (20-week-old) mice that have been fed with high-fat diet for 13 weeks were treated with 7,8-DHF for 9 weeks. Various biochemical and molecular analyses were performed to examine the signal transduction pathway, metabolite content, and mitochondrial mass in the animals. Moreover, systemic energy metabolism and insulin sensitivity were determined by indirect calorimetry and insulin/glucose-tolerance tests. We have also determined the metabolic actions of 7,8-DHF on cultured myotubes. Results: 7,8-DHF treatment increased cellular respiration by promoting mitochondrial biogenesis in cultured skeletal muscle cells. In diet-induced obese mice, subsequent 7,8-DHF consumption triggered the AMPK/CREB/PGC-1α pathways to increase the muscular mitochondrial content. Systemic energy metabolism was thus elevated, which reduced the body weight gain in obese animals. Consequently, hyperlipidemia, hyperglycemia hyperinsulinemia, and ectopic lipid accumulation in skeletal muscle and liver of the obese animals were alleviated after 7,8-DHF treatment. Moreover, insulin sensitivity of the obese muscle was improved after 7,8-DHF consumption. Conclusion: 7,8-DHF treatment increases muscular mitochondrial respiration and systemic energy expenditure, which alleviates the body weight gain and partially reverse the metabolic abnormalities induced by obesity. © 2018 Elsevier Inc. |
Persistent Identifier | http://hdl.handle.net/10722/256199 |
ISSN | 2023 Impact Factor: 10.8 2023 SCImago Journal Rankings: 2.792 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wood, J | - |
dc.contributor.author | Tse, CL | - |
dc.contributor.author | Yang, X | - |
dc.contributor.author | Brobst, D | - |
dc.contributor.author | Liu, Z | - |
dc.contributor.author | Zaw, AM | - |
dc.contributor.author | Chow, BKC | - |
dc.contributor.author | Lee, CW | - |
dc.contributor.author | Chan, CB | - |
dc.date.accessioned | 2018-07-20T06:30:53Z | - |
dc.date.available | 2018-07-20T06:30:53Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Metabolism, 2018, v. 87, p. 113-122 | - |
dc.identifier.issn | 0026-0495 | - |
dc.identifier.uri | http://hdl.handle.net/10722/256199 | - |
dc.description.abstract | Background: 7,8-Dihydroxyflavone (7,8-DHF) is a small molecular weight compound that mimics the functions of brain-derived neurotrophic factor (BDNF). The current study aims to elucidate the molecular mechanism of 7,8-DHF-induced body weight regulation. Methods: Obese female C57/BL6 (20-week-old) mice that have been fed with high-fat diet for 13 weeks were treated with 7,8-DHF for 9 weeks. Various biochemical and molecular analyses were performed to examine the signal transduction pathway, metabolite content, and mitochondrial mass in the animals. Moreover, systemic energy metabolism and insulin sensitivity were determined by indirect calorimetry and insulin/glucose-tolerance tests. We have also determined the metabolic actions of 7,8-DHF on cultured myotubes. Results: 7,8-DHF treatment increased cellular respiration by promoting mitochondrial biogenesis in cultured skeletal muscle cells. In diet-induced obese mice, subsequent 7,8-DHF consumption triggered the AMPK/CREB/PGC-1α pathways to increase the muscular mitochondrial content. Systemic energy metabolism was thus elevated, which reduced the body weight gain in obese animals. Consequently, hyperlipidemia, hyperglycemia hyperinsulinemia, and ectopic lipid accumulation in skeletal muscle and liver of the obese animals were alleviated after 7,8-DHF treatment. Moreover, insulin sensitivity of the obese muscle was improved after 7,8-DHF consumption. Conclusion: 7,8-DHF treatment increases muscular mitochondrial respiration and systemic energy expenditure, which alleviates the body weight gain and partially reverse the metabolic abnormalities induced by obesity. © 2018 Elsevier Inc. | - |
dc.language | eng | - |
dc.publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/metabol | - |
dc.relation.ispartof | Metabolism | - |
dc.subject | 7,8-Dihydroxyflavone | - |
dc.subject | Mitochondrial | - |
dc.subject | Obesity | - |
dc.subject | Skeletal muscle | - |
dc.title | BDNF mimetic alleviates body weight gain in obese mice by enhancing mitochondrial biogenesis in skeletal muscle | - |
dc.type | Article | - |
dc.identifier.email | Tse, CL: tsecl@hku.hk | - |
dc.identifier.email | Zaw, AM: aungmoe@HKUCC-COM.hku.hk | - |
dc.identifier.email | Chow, BKC: bkcc@hku.hk | - |
dc.identifier.email | Lee, CW: chiwai.lee@hku.hk | - |
dc.identifier.email | Chan, CB: chancb@hku.hk | - |
dc.identifier.authority | Chow, BKC=rp00681 | - |
dc.identifier.authority | Lee, CW=rp02089 | - |
dc.identifier.authority | Chan, CB=rp02140 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.metabol.2018.06.007 | - |
dc.identifier.pmid | 29935237 | - |
dc.identifier.scopus | eid_2-s2.0-85050402133 | - |
dc.identifier.hkuros | 286108 | - |
dc.identifier.volume | 87 | - |
dc.identifier.spage | 113 | - |
dc.identifier.epage | 122 | - |
dc.identifier.isi | WOS:000454746800015 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0026-0495 | - |