The potential benefit of leptin therapy against amyotrophic lateral sclerosis (ALS)

Background Targeting leptin could represent a rational strategy to treat amyotrophic lateral sclerosis (ALS), as previously clinical studies have shown its levels to be associated with a lower risk of ALS disease. However, very little is known about the potential influence of leptin in altering disease progression in ALS, as it has thus far been correlated with the protection exerted by increased fat mass stores. Methods We studied the impact of leptin treatment beginning at 42-days of age (asymptomatic stage of disease) in the TDP-43 (TDP43(A315T)) transgenic (Tg) ALS mouse model. Results Our study shows that leptin treatment was associated with altered expression of adipokines and metabolic proteins in TDP43(A315T) mice. We also observed that weight loss decline was less prominent after leptin treatment in TDP43(A315T) mice relative to vehicle-treated animals. In TDP43(A315T) mice treated with leptin the disease duration lasted longer along with an improvement in motor performance relative to vehicle-treated animals. Conclusions Collectively, our results support leptin as a potential novel treatment approach for ALS.

Automated summary

The study found that leptin treatment in the ALS mouse model altered expression of adipokines and metabolic proteins, reduced weight loss decline, prolonged disease duration, and improved motor performance. This suggests that leptin could be a potential novel treatment approach for ALS.