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It is the only GHRH analog with FDA-recognized studies specifically demonstrating its ability to reduce visceral adipose tissue (VAT) the dangerous fat that surrounds abdominal organs and is associated with cardiovascular disease, insulin resistance, and metabolic syndrome
doi: 10.1007/s43032-023-01394-7
The resulting nanosponge network is susceptible to degradation by endogenous biomolecules, including glutathione and esterase enzymes, enabling a triggered structural breakdown that releases the antimicrobial payload at the infection site
In published preclinical literature, the individual KLOW components have been characterized across hypothalamic-pituitary-gonadal-axis research (Kisspeptin-10), antimicrobial peptide and tissue-remodeling research (LL-37), neuropeptide-signaling research (Oxytocin), and tissue-remodeling and angiogenesis research (Wolverine Blend)
Sandrin L, Tanter M, Gennisson JL, et al
