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Intranasal GHK peptide enhances resilience to cognitive decline in aging mice. | LitMetric

AI Article Synopsis

  • Brain aging leads to common cognitive impairments in older adults, with early cognitive decline being particularly prevalent and linked to increased dementia risk.
  • Recent research indicates that GHK-Cu, a naturally occurring peptide, shows promise in treating age-related cognitive decline by potentially enhancing cognitive functions and reducing neuroinflammation.
  • In studies with aged mice, those treated with intranasal GHK-Cu demonstrated improved memory and learning abilities, paving the way for further exploration of this treatment in future clinical trials.

Article Abstract

Brain aging and cognitive decline are aspects of growing old. Age-related cognitive impairment entails the early stages of cognitive decline, and is extremely common, affecting millions of older people. Investigation into early cognitive decline as a treatable condition is relevant to a wide range of cognitive impairment conditions, since mild age-related neuropathology increases risk for more severe neuropathology and dementia associated with Alzheimer's Disease. Recent studies suggest that the naturally occurring peptide GHK (glycyl-L-histidyl-L-lysine) in its Cu-bound form, has the potential to treat cognitive decline associated with aging. In order to test this concept, male and female C57BL/6 mice, 20 months of age, were given intranasal GHK-Cu, 15 mg/kg daily, for two months. Results showed that mice treated with intranasal GHK-Cu had an enhanced level of cognitive performance in spatial memory and learning navigation tasks, and expressed decreased neuroinflammatory and axonal damage markers compared to mice treated with intranasal saline. These observations suggest that GHK-Cu can enhance resilience to brain aging, and has translational implications for further testing in both preclinical and clinical studies using an atomizer device for intranasal delivery.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680828PMC
http://dx.doi.org/10.1101/2023.11.16.567423DOI Listing

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