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What Research Shows

Introduction:

AOD-9604 is a synthetic peptide fragment of human growth hormone (HGH), designed to selectively target fat metabolism without stimulating growth pathways.¹ While initially developed for obesity research, studies have also suggested potential benefits for metabolism, lipid balance, and cartilage protection.

Because AOD-9604 remains an experimental peptide, all reported benefits are based on preclinical models and early clinical work, not established medical evidence.

Potential Benefits of AOD-9604

AOD-9604 has been studied for fat metabolism, weight regulation, and cartilage protection.

1. Fat Breakdown (Lipolysis)

  • AOD-9604 promotes the breakdown of stored triglycerides into free fatty acids.¹
  • This effect has been observed in adipose tissue from both lean and obese models.

Key takeaway: May support the mobilization of stored fat for energy.

2. Reduced Fat Storage (Anti-Lipogenesis)

  • Research shows AOD-9604 can inhibit the formation of new fat from dietary carbohydrates.²
  • In obese rodent models, this led to less weight gain even under high-calorie diets.

 Key takeaway: Suggests potential use in preventing fat accumulation.

3. Weight Regulation

  • In animal studies, AOD-9604 reduced body fat mass and improved metabolic parameters.²
  • Early human trials showed limited direct weight loss, but trends toward improved lipid metabolism.³

Key takeaway: May influence weight management indirectly by altering fat metabolism.

4. Lipid Profile & Metabolic Health

  • Some research reports improved lipid balance (e.g., triglyceride reduction) in preclinical studies.²
  • Possible improvements in basal metabolic rate have also been noted.

Key takeaway: Beyond fat burning, AOD-9604 may have broader metabolic effects.

5. Cartilage & Joint Protection

Because DSIP is often studied for sleep regulation, it is natural to compare it with melatonin, the most widely used sleep supplement:

  • AOD-9604 demonstrated chondroprotective effects in models of cartilage degradation.⁴
  • May reduce proteoglycan loss and support collagen maintenance.

Key takeaway: Suggests possible relevance for joint and connective tissue research.

Limitations of Evidence

  • Animal-dominant data: Most findings are from rodent and cell models.
  • Human trials limited: Clinical data shows modest or inconsistent results.³
  • Unclear mechanisms in humans: Translation from animals to people remains uncertain.

Summary

Research into AOD-9604 suggests potential benefits for:

  • Fat breakdown (lipolysis)
  • Reduced fat storage (anti-lipogenesis)
  • Weight regulation
  • Improved lipid profile
  • Cartilage protection

However, AOD-9604 remains an experimental peptide, with human results still inconclusive.died but potentially broader in scope, influencing multiple systems beyond sleep.

FAQs About AOD-9604 Benefits

What is the main benefit of AOD-9604?

 Research suggests its primary effect is fat metabolism — stimulating fat breakdown and reducing fat storage.

Can AOD-9604 help with weight loss?

  Animal studies show fat loss effects, but human results have been mixed.

Does AOD-9604 support joint health?

 Some early research suggests cartilage-protective effects.

Is AOD-9604 approved for obesity treatment?

 No — AOD-9604 is not FDA-approved and remains a research-only peptide.

Related Articles

References

  1. Heffernan M, et al. “AOD9604, a novel fragment of human growth hormone, stimulates lipolysis in adipose tissue.” J Endocrinol. 2001;170(3):433–442. https://pubmed.ncbi.nlm.nih.gov/11479127/
  2. Ng FM, et al. “Metabolic effects of a growth hormone fragment (AOD9604) in obese Zucker rats.” Obes Res. 2000;8(6):479–486. https://pubmed.ncbi.nlm.nih.gov/11156424/
  3. Ng FM, et al. “AOD9604, an analog of hGH fragment 177–191, reduces body weight in obese mice but not obese humans.” Int J Obes Relat Metab Disord. 2002;26(2):191–197. https://pubmed.ncbi.nlm.nih.gov/11850748/
  4. Ng FM, et al. “Chondroprotective potential of AOD9604 in cartilage degradation models.” Arthritis Res Ther. 2004;6(6):R713–R722. https://pubmed.ncbi.nlm.nih.gov/15535832/