Genetic induction of hypometabolism by ablation of MC4R does not suppress ALS-like phenotypes in the G93A mutant SOD1 mouse model

Sci Rep. 2017 Oct 13;7(1):13150. doi: 10.1038/s41598-017-13304-4.


Dysfunction and death of motor neurons leads to progressive paralysis in amyotrophic lateral sclerosis (ALS). Recent studies have reported organism-level metabolic dysfunction as a prominent but poorly understood feature of the disease. ALS patients are hypermetabolic with increased resting energy expenditure, but if and how hypermetabolism contributes to disease pathology is unknown. We asked if decreasing metabolism in the mutant superoxide dismutase 1 (SOD1) mouse model of ALS (G93A SOD1) would alter motor function and survival. To address this, we generated mice with the G93A SOD1 mutation that also lacked the melanocortin-4 receptor (MC4R). MC4R is a critical regulator of energy homeostasis and food intake in the hypothalamus. Loss of MC4R is known to induce hyperphagia and hypometabolism in mice. In the MC4R null background, G93A SOD1 mice become markedly hypometabolic, overweight and less active. Decreased metabolic rate, however, did not reverse any ALS-related disease phenotypes such as motor dysfunction or decreased lifespan. While hypermetabolism remains an intriguing target for intervention in ALS patients and disease models, our data indicate that the melanocortin system is not a good target for manipulation. Investigating other pathways may reveal optimal targets for addressing metabolic dysfunction in ALS.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amyotrophic Lateral Sclerosis / genetics*
  • Animals
  • Carbon Dioxide / metabolism
  • Disease Models, Animal
  • Female
  • Genotype
  • Male
  • Mice
  • Mice, Knockout
  • Motor Neurons / metabolism
  • Mutation / genetics
  • Oxygen Consumption / genetics
  • Oxygen Consumption / physiology
  • Receptor, Melanocortin, Type 4 / deficiency*
  • Receptor, Melanocortin, Type 4 / genetics
  • Superoxide Dismutase-1 / genetics*


  • Receptor, Melanocortin, Type 4
  • Carbon Dioxide
  • Superoxide Dismutase-1