Investigation of cellular and molecular targets in the brain of mice given intranasal GHK peptide to treat age-related cognitive decline
| dc.contributor.advisor | Ladiges, Warren | |
| dc.contributor.author | Rosenfeld, Manuela | |
| dc.date.accessioned | 2025-08-01T22:13:10Z | |
| dc.date.available | 2025-08-01T22:13:10Z | |
| dc.date.issued | 2025-08-01 | |
| dc.date.submitted | 2025 | |
| dc.description | Thesis (Master's)--University of Washington, 2025 | |
| dc.description.abstract | There are currently 1.2 billion people worldwide over the age of 60 and this number is projected to double by 2050. With the world population over 60 reaching 22% within the next 50 years, there is an increasing need to understand the mechanisms and processes of aging. An area of major interest is brain aging given that approximately 2 out of 3 Americans experience some level of cognitive impairment by age 70. Neuropathology associated with this cognitive impairment can lead to more severe neuropathology associated with Alzheimer’s disease and other dementias providing a need to develop interventions to treat and potentially prevent or reverse age related cognitive decline. One particular therapeutic of interest is a naturally occurring peptide called glycyl-L-histidyl-L-lysine (GHK) as recent studies suggest that GHK in its Cu bound form has the potential to age related cognitive decline. In order to further investigate the potential of GHK-Cu as a therapeutic for age related cognitive decline, mouse hippocampal tissue from 20-month-old C57BL/6 mice treated with 15mg/kg of intranasal GHK-Cu daily for 8 weeks were used for immunohistochemistry and RNA sequencing to discover cellular and molecular targets of this peptide. Results suggested that mice treated with intranasal GHK-Cu had lower expression of potentially harmful astrocytes. RNA sequencing results revealed that mice treated with GHK-Cu had upregulation or downregulation of various gene pathways in a way that supports healthy brain aging. Sex differences were also observed with certain pathways being affected differently in males and females. These findings provide rationale for further investigation of GHK-Cu as a therapeutic for age related cognitive decline in preclinical and clinical studies. | |
| dc.embargo.terms | Open Access | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.other | Rosenfeld_washington_0250O_28536.pdf | |
| dc.identifier.uri | https://hdl.handle.net/1773/53342 | |
| dc.language.iso | en_US | |
| dc.rights | none | |
| dc.subject | Aging | |
| dc.subject.other | Comparative medicine | |
| dc.title | Investigation of cellular and molecular targets in the brain of mice given intranasal GHK peptide to treat age-related cognitive decline | |
| dc.type | Thesis |
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