Chemotherapy-induced cognitive impairment (CICI) has emerged as a significant medical problem without therapeutic options. Using the platinum-based chemotherapy cisplatin to model CICI, we revealed robust elevations in the adenosine A receptor (AR) and its downstream effectors, cAMP and CREB, by cisplatin in the adult mouse hippocampus, a critical brain structure for learning and memory. Notably, AR inhibition by the Food and Drug Administration-approved AR antagonist KW-6002 prevented cisplatin-induced impairments in neural progenitor proliferation and dendrite morphogenesis of adult-born neurons, while improving memory and anxiety-like behavior, without affecting tumor growth or cisplatin's antitumor activity. Collectively, our study identifies AR signaling as a key pathway that can be therapeutically targeted to prevent cisplatin-induced cognitive impairments.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282426 | PMC |
http://dx.doi.org/10.1073/pnas.2206415119 | DOI Listing |
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