AOD-9604's primary research application is the stimulation of lipolysis — the breakdown of stored triglycerides in adipose (fat) tissue. Research by Ng et al. at Monash University demonstrated that AOD-9604 stimulated lipolysis in rodent adipose tissue explants at levels comparable to full-length growth hormone, but without the accompanying increase in IGF-1 levels.1
The lipolytic mechanism is thought to involve activation of the beta-3 adrenergic receptor pathway in adipocytes, which triggers hormone-sensitive lipase to release fatty acids from stored triglycerides. Unlike full-length GH, which stimulates lipolysis through both direct adipocyte effects and indirect IGF-1-mediated pathways, AOD-9604 appears to act only through the direct pathway.2
In obese Zucker rat models, chronic AOD-9604 administration reduced body fat percentage without affecting lean mass, food intake, or growth. This selectivity — reducing fat without affecting other growth parameters — is the key property that distinguishes AOD-9604 from full-length growth hormone.






