K4 Elite
Humanin is a 24-amino-acid mitochondrial-derived peptide encoded within the MT-RNR2 (16S rRNA) region, first identified for its cytoprotective and antiapoptotic activity. It is studied in the context of cellular stress resistance, metabolism, and neuroprotection, and is offered strictly for laboratory research.
Humanin is a 24-amino-acid peptide encoded within the mitochondrial 16S ribosomal RNA gene (MT-RNR2). It was first identified in the early 2000s from surviving neurons in Alzheimer-affected brain tissue and characterized by its antiapoptotic, cytoprotective properties. It is one of the founding members of the mitochondrial-derived peptide (MDP) family.
Research has explored humanin and its more potent analog HNG (with a Ser14Gly substitution) across neuronal survival, metabolic regulation, and cellular stress-response contexts. Circulating humanin levels have been reported to decline with age, which has driven interest in its role in longevity biology.
Content here summarizes peer-reviewed literature. Humanin is intended for research use only and is not a drug, supplement, or approved therapy.
Humanin is reported to exert cytoprotective effects through multiple pathways. It interacts with the pro-apoptotic protein Bax and with insulin-like growth factor-binding protein 3 (IGFBP-3), and it binds a trimeric receptor complex (CNTFR-alpha / gp130 / WSX-1) that activates JAK2/STAT3 signaling. Studies also report activation of ERK1/2 and AKT pathways.
In metabolic models, humanin has been associated with improved insulin sensitivity via hypothalamic STAT3 signaling. These mechanisms have been characterized largely in cell-culture and rodent systems.
Reporting only — not guidance. Hashimoto et al. (2001, PNAS) identified humanin and characterized its ability to suppress neuronal cell death induced by Alzheimer-related insults in cell culture, defining its antiapoptotic activity.
Muzumdar et al. (2009, Endocrinology) administered the humanin analog HNG to rodents and reported improvements in insulin sensitivity and glucose metabolism, describing metabolic effects in an animal model. Cai et al. (2017) reported that humanin activates ERK1/2, AKT, and STAT3 signaling in the hippocampus with age-dependent differences. These are descriptions of published experiments, not protocols for use.
Combinations examined in the research literature. Descriptive only — not a recommendation to combine compounds.