Literature DB >> 28051332

Activation of the central melanocortin system chronically reduces body mass without the necessity of long-term caloric restriction.

I Côté1, Y Sakarya1,2, N Kirichenko1,2, D Morgan3, C S Carter4, N Tümer1,2, P J Scarpace1.   

Abstract

Melanotan II (MTII) is a potent appetite suppressor that rapidly reduces body mass. Given the rapid loss of anorexic response upon chronic MTII treatment, most investigations have focused on the initial physiological adaptations. However, other evidence supports MTII as a long-term modulator of energy balance that remains to be established. Therefore, we examined the chronic effects of MTII on energy homeostasis. MTII (high or low dose) or artificial cerebrospinal fluid (aCSF) was infused into the lateral ventricle of the brain of 6-month-old F344BN rats (6-7/group) over 40 days. MTII suppressed appetite in a dose-dependent manner (P < 0.05). Although food intake promptly rose back to control level, body mass was persistently reduced in both MTII groups (P < 0.01). At day 40, both MTII groups displayed lower adiposity than the aCSF animals (P < 0.01). These results show that MTII chronically reduces body mass without the requirement of long-term caloric restriction. Our study proposes that food restriction helps initiate mass loss; however, combined with a secondary pharmacological approach preserving a negative energy balance state over time may help combat obesity.

Entities:  

Keywords:  MTII; apport alimentaire; body mass; central melanocortin system; food intake; lean body mass; masse corporelle; masse corporelle maigre; système de la mélanocortine central

Mesh:

Substances:

Year:  2016        PMID: 28051332      PMCID: PMC5572812          DOI: 10.1139/cjpp-2016-0290

Source DB:  PubMed          Journal:  Can J Physiol Pharmacol        ISSN: 0008-4212            Impact factor:   2.273


  43 in total

1.  Aged-obese rats exhibit robust responses to a melanocortin agonist and antagonist despite leptin resistance.

Authors:  Yi Zhang; Michael Matheny; Nihal Tümer; Philip J Scarpace
Journal:  Neurobiol Aging       Date:  2004 Nov-Dec       Impact factor: 4.673

2.  Central infusion of the melanocortin receptor antagonist agouti-related peptide (AgRP(83-132)) prevents cachexia-related symptoms induced by radiation and colon-26 tumors in mice.

Authors:  M A Joppa; K R Gogas; A C Foster; S Markison
Journal:  Peptides       Date:  2007-01-03       Impact factor: 3.750

3.  Targeted disruption of the melanocortin-4 receptor results in obesity in mice.

Authors:  D Huszar; C A Lynch; V Fairchild-Huntress; J H Dunmore; Q Fang; L R Berkemeier; W Gu; R A Kesterson; B A Boston; R D Cone; F J Smith; L A Campfield; P Burn; F Lee
Journal:  Cell       Date:  1997-01-10       Impact factor: 41.582

4.  Long-term weight-loss maintenance: a meta-analysis of US studies.

Authors:  J W Anderson; E C Konz; R C Frederich; C L Wood
Journal:  Am J Clin Nutr       Date:  2001-11       Impact factor: 7.045

Review 5.  The use of a running wheel to measure activity in rodents: relationship to energy balance, general activity, and reward.

Authors:  Colleen M Novak; Paul R Burghardt; James A Levine
Journal:  Neurosci Biobehav Rev       Date:  2012-01-02       Impact factor: 8.989

6.  A unique metabolic syndrome causes obesity in the melanocortin-3 receptor-deficient mouse.

Authors:  A A Butler; R A Kesterson; K Khong; M J Cullen; M A Pelleymounter; J Dekoning; M Baetscher; R D Cone
Journal:  Endocrinology       Date:  2000-09       Impact factor: 4.736

7.  Genetic and pharmacologic blockade of central melanocortin signaling attenuates cardiac cachexia in rodent models of heart failure.

Authors:  Jarrad M Scarlett; Darren D Bowe; Xinxia Zhu; Ayesha K Batra; Wilmon F Grant; Daniel L Marks
Journal:  J Endocrinol       Date:  2010-04-06       Impact factor: 4.286

Review 8.  The melanocortin receptors: lessons from knockout models.

Authors:  A A Butler; R D Cone
Journal:  Neuropeptides       Date:  2002 Apr-Jun       Impact factor: 3.286

9.  Hypothalamic agouti-related protein messenger ribonucleic acid is inhibited by leptin and stimulated by fasting.

Authors:  T M Mizuno; C V Mobbs
Journal:  Endocrinology       Date:  1999-02       Impact factor: 4.736

10.  Mechanisms underlying obesity resistance associated with high spontaneous physical activity.

Authors:  J A Teske; C J Billington; C M Kotz
Journal:  Neuroscience       Date:  2013-10-22       Impact factor: 3.590

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  1 in total

Review 1.  The melanocortin pathway and control of appetite-progress and therapeutic implications.

Authors:  Giulia Baldini; Kevin D Phelan
Journal:  J Endocrinol       Date:  2019-04-01       Impact factor: 4.286

  1 in total

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