Cargando…

Loss of hypothalamic MCH decreases food intake in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) is associated with impaired energy metabolism, including weight loss and decreased appetite which are negatively correlated with survival. Neural mechanisms underlying metabolic impairment in ALS remain unknown. ALS patients and presymptomatic gene carriers have e...

Descripción completa

Detalles Bibliográficos
Autores principales: Bolborea, Matei, Vercruysse, Pauline, Daria, Tselmen, Reiners, Johanna C., Alami, Najwa Ouali, Guillot, Simon J., Dieterlé, Stéphane, Sinniger, Jérôme, Scekic-Zahirovic, Jelena, Londo, Amela, Arcay, Hippolyte, Goy, Marc-Antoine, de Tapia, Claudia Nelson, Thal, Dietmar R., Shibuya, Kazumoto, Otani, Ryo, Arai, Kimihito, Kuwabara, Satoshi, Ludolph, Albert C., Roselli, Francesco, Yilmazer-Hanke, Deniz, Dupuis, Luc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10175407/
https://www.ncbi.nlm.nih.gov/pubmed/37058170
http://dx.doi.org/10.1007/s00401-023-02569-x
Descripción
Sumario:Amyotrophic lateral sclerosis (ALS) is associated with impaired energy metabolism, including weight loss and decreased appetite which are negatively correlated with survival. Neural mechanisms underlying metabolic impairment in ALS remain unknown. ALS patients and presymptomatic gene carriers have early hypothalamic atrophy. The lateral hypothalamic area (LHA) controls metabolic homeostasis through the secretion of neuropeptides such as orexin/hypocretin and melanin-concentrating hormone (MCH). Here, we show loss of MCH-positive neurons in three mouse models of ALS based on SOD1 or FUS mutations. Supplementation with MCH (1.2 µg/d) through continuous intracerebroventricular delivery led to weight gain in male mutant Sod1(G86R) mice. MCH supplementation increased food intake, rescued expression of the key appetite-related neuropeptide AgRP (agouti-related protein) and modified respiratory exchange ratio, suggesting increased carbohydrate usage during the inactive phase. Importantly, we document pTDP-43 pathology and neurodegeneration in the LHA of sporadic ALS patients. Neuronal cell loss was associated with pTDP-43-positive inclusions and signs of neurodegeneration in MCH-positive neurons. These results suggest that hypothalamic MCH is lost in ALS and contributes to the metabolic changes, including weight loss and decreased appetite. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00401-023-02569-x.