The metabolic phenotype of SCD1-deficient mice is independent of melanin-concentrating hormone.

Melissa B Glier, Pavlos Pissios, Sandra L Babich, Marcia L E Macdonald, Michael R Hayden, Eleftheria Maratos-Flier, William T Gibson
Author Information
  1. Melissa B Glier: Department of Medical Genetics, Child and Family Research Institute, University of British Columbia, Canada. glier@interchange.ubc.ca

Abstract

We propose that deletion of pro-melanin-concentrating hormone (pMCH) would increase energy expenditure and further improve glucose tolerance in mice lacking stearoyl-coA desaturase-1 (SCD1). To test our hypothesis, we bred and metabolically challenged Pmch-/-; Scd1-/- double-knockout mice, with comparison to Pmch-/- mice; Scd1-/- mice and C57Bl/6J controls. Deletion of both Pmch and Scd1 increased both food intake and energy expenditure relative to control mice. Pmch-/-; Scd1-/- double-knockout mice had improved glucose tolerance relative to control mice. The majority of the metabolic effects were contributed by inactivation of the Scd1 gene. We conclude that the increased food intake and increased energy expenditure of Scd1-/- mice are independent of the neuropeptide melanin-concentrating hormone.

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Grants

  1. P30 DK057521/NIDDK NIH HHS
  2. OOP-79614/CIHR

MeSH Term

Animals
Body Weight
Eating
Energy Metabolism
Female
Genotype
Glucose Tolerance Test
Homeostasis
Humans
Hypothalamic Hormones
Insulin
Mice
Mice, Inbred C57BL
Mice, Knockout
Motor Activity
Protein Precursors
Stearoyl-CoA Desaturase

Chemicals

Hypothalamic Hormones
Insulin
Protein Precursors
melanin-concentrating hormone precursors
Stearoyl-CoA Desaturase

Word Cloud

Created with Highcharts 10.0.0miceScd1-/-hormoneenergyexpenditurePmch-/-increasedglucosetolerancedouble-knockoutScd1foodintakerelativecontrolmetabolicindependentmelanin-concentratingproposedeletionpro-melanin-concentratingpMCHincreaseimprovelackingstearoyl-coAdesaturase-1SCD1testhypothesisbredmetabolicallychallengedcomparisonC57Bl/6JcontrolsDeletionPmchimprovedmajorityeffectscontributedinactivationgeneconcludeneuropeptidephenotypeSCD1-deficient

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