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As we age, declining growth hormone levels make fat loss increasingly difficult especially that persistent visceral fat around the midsection
et al: GLP-1RA and SGLT2i Medications for Type 2 Diabetes and Alzheimer Disease and Related Dementias. JAMA Neurology, April 7, 2025
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L-Carnitine supplementation was shown to attenuate this post-exercise downregulation, maintaining higher androgen receptor density during the recovery period The practical implication for AAS users: more androgen receptors in muscle during the recovery period means more receptor availability for the exogenous androgens circulating from the cycle potentially enhancing the anabolic signalling from a given AAS dose This effect was observed at plasma L-Carnitine concentrations achievable by injectable supplementation but difficult to achieve reliably with oral supplementation given the bioavailability gap Effects and Benefits Enhanced fatty acid transport into mitochondria via CPT shuttle saturation maximises fat oxidation during fasted training and aerobic work Androgen receptor upregulation in muscle tissue maintains receptor density during post-exercise recovery, potentially enhancing AAS anabolic signalling Reduced exercise-induced muscle damage markers in some studies potentially faster recovery between sessions No hormonal suppression does not affect testosterone, HPG axis or require PCT Near-complete bioavailability versus 14-18% oral absorption Dosage and Administration At 500mg/ml, a 2ml injection delivers 1,000mg
Type 1 diabetes : GLP-1 receptor agonists are not approved for treating type 1 diabetes
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