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Article: Dietary fat concentration influences the effects of trans-10, cis-12 conjugated linoleic acid on temporal patterns of energy Intake and Hypothalamic expression of appetite-controlling genes in Mice
Title | Dietary fat concentration influences the effects of trans-10, cis-12 conjugated linoleic acid on temporal patterns of energy Intake and Hypothalamic expression of appetite-controlling genes in Mice |
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Authors | |
Issue Date | 2009 |
Publisher | American Society for Nutrition. The Journal's web site is located at http://jn.nutrition.org |
Citation | Journal Of Nutrition, 2009, v. 139 n. 1, p. 145-151 How to Cite? |
Abstract | This study tested the hypothesis that the effect of trans-10, c/s-12 conjugated linoleic acid (t10, c12 CLA) on energy intake (EI) and body weight (BW)/composition is confounded by dietary fat concentration and involves hypothalamic appetite-controlling mechanisms. ICR mice received low-fat (LF; 5g/100g) or high-fat (HF;30g/100g) diets, with or without 0.5 g/100 g t10, c12 CLA (>98% pure) for 27 d. By d 13, BW and cumulative EI of the mice fed CLA supplemented LF diet (LF/CLA) were 6.6 and 23.6% lower, respectively, than the LF mice. In the subsequent 14 d, their EI rebounded and did not differ from the LF group. BW and EI did not differ between the HF and CLA supplemented HF (HF/CLA) groups. Hypothalamic pro-opiomelanocortin (POMC) mRNA expression was elevated (P = 0.031) on d 13 but suppressed (P< 0.001) on d 27 due to CLA treatment. CLA also suppressed AMP-activated protein kinase α2 expression. Mice in Expt. 2 received the LF diet, the LF/CLA, or were pair-fed the LF diet to the EI of the CLA group (LF/PF). LF/CLA and LF/PF mice did not differ in the hypothalamic POMC:neuropeptide Y expression ratio on d 13, but it was significantly lower in the LF/PF group on d 27. We conclude that the habitual dietary fat concentration influences the magnitude of weight loss induced by dietary t10, c12 CLA. The effect is in part independent of EI. Hypothalamic neuropeptides and nutrient sensing mechanisms may play a role. © 2009 American Society for Nutrition. |
Persistent Identifier | http://hdl.handle.net/10722/179113 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.098 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | So, MHH | en_US |
dc.contributor.author | Tse, IMY | en_US |
dc.contributor.author | Li, ETS | en_US |
dc.date.accessioned | 2012-12-19T09:52:04Z | - |
dc.date.available | 2012-12-19T09:52:04Z | - |
dc.date.issued | 2009 | en_US |
dc.identifier.citation | Journal Of Nutrition, 2009, v. 139 n. 1, p. 145-151 | en_US |
dc.identifier.issn | 0022-3166 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/179113 | - |
dc.description.abstract | This study tested the hypothesis that the effect of trans-10, c/s-12 conjugated linoleic acid (t10, c12 CLA) on energy intake (EI) and body weight (BW)/composition is confounded by dietary fat concentration and involves hypothalamic appetite-controlling mechanisms. ICR mice received low-fat (LF; 5g/100g) or high-fat (HF;30g/100g) diets, with or without 0.5 g/100 g t10, c12 CLA (>98% pure) for 27 d. By d 13, BW and cumulative EI of the mice fed CLA supplemented LF diet (LF/CLA) were 6.6 and 23.6% lower, respectively, than the LF mice. In the subsequent 14 d, their EI rebounded and did not differ from the LF group. BW and EI did not differ between the HF and CLA supplemented HF (HF/CLA) groups. Hypothalamic pro-opiomelanocortin (POMC) mRNA expression was elevated (P = 0.031) on d 13 but suppressed (P< 0.001) on d 27 due to CLA treatment. CLA also suppressed AMP-activated protein kinase α2 expression. Mice in Expt. 2 received the LF diet, the LF/CLA, or were pair-fed the LF diet to the EI of the CLA group (LF/PF). LF/CLA and LF/PF mice did not differ in the hypothalamic POMC:neuropeptide Y expression ratio on d 13, but it was significantly lower in the LF/PF group on d 27. We conclude that the habitual dietary fat concentration influences the magnitude of weight loss induced by dietary t10, c12 CLA. The effect is in part independent of EI. Hypothalamic neuropeptides and nutrient sensing mechanisms may play a role. © 2009 American Society for Nutrition. | en_US |
dc.language | eng | en_US |
dc.publisher | American Society for Nutrition. The Journal's web site is located at http://jn.nutrition.org | en_US |
dc.relation.ispartof | Journal of Nutrition | en_US |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Appetite - Physiology | en_US |
dc.subject.mesh | Dietary Fats - Administration & Dosage - Pharmacology | en_US |
dc.subject.mesh | Dose-Response Relationship, Drug | en_US |
dc.subject.mesh | Feeding Behavior | en_US |
dc.subject.mesh | Gene Expression Profiling | en_US |
dc.subject.mesh | Gene Expression Regulation - Drug Effects - Physiology | en_US |
dc.subject.mesh | Hypothalamus - Metabolism | en_US |
dc.subject.mesh | Linoleic Acids, Conjugated - Pharmacology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Mice | en_US |
dc.subject.mesh | Mice, Inbred Icr | en_US |
dc.subject.mesh | Rna, Messenger - Genetics - Metabolism | en_US |
dc.subject.mesh | Time Factors | en_US |
dc.subject.mesh | Weight Gain - Drug Effects | en_US |
dc.title | Dietary fat concentration influences the effects of trans-10, cis-12 conjugated linoleic acid on temporal patterns of energy Intake and Hypothalamic expression of appetite-controlling genes in Mice | en_US |
dc.type | Article | en_US |
dc.identifier.email | Li, ETS: etsli@hku.hk | en_US |
dc.identifier.authority | Li, ETS=rp00737 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.3945/jn.108.093849 | en_US |
dc.identifier.pmid | 19056663 | - |
dc.identifier.scopus | eid_2-s2.0-58649117155 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-58649117155&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 139 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 145 | en_US |
dc.identifier.epage | 151 | en_US |
dc.identifier.eissn | 1541-6100 | - |
dc.identifier.isi | WOS:000261777100025 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | So, MHH=36719005000 | en_US |
dc.identifier.scopusauthorid | Tse, IMY=14635211700 | en_US |
dc.identifier.scopusauthorid | Li, ETS=14018169600 | en_US |
dc.identifier.issnl | 0022-3166 | - |