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腺苷 A 受体阻断可预防顺铂诱导的神经发生和认知功能障碍。

Adenosine A receptor blockade prevents cisplatin-induced impairments in neurogenesis and cognitive function.

机构信息

Neurologic Surgery, Mayo Clinic, Rochester, MN 55905.

Neurosurgery, Robert Wood Johnson Medical School, Rutgers University, Piscataway, NJ 08854.

出版信息

Proc Natl Acad Sci U S A. 2022 Jul 12;119(28):e2206415119. doi: 10.1073/pnas.2206415119. Epub 2022 Jul 7.

Abstract

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.

摘要

化疗引起的认知障碍(CICI)是一个没有治疗选择的重要医学问题。我们使用基于铂的化疗药物顺铂来模拟 CICI,发现顺铂在成年小鼠海马体中显著增加了腺苷 A 受体(AR)及其下游效应物 cAMP 和 CREB 的水平,海马体是学习和记忆的关键脑区。值得注意的是,美国食品和药物管理局批准的 AR 拮抗剂 KW-6002 抑制 AR,可防止顺铂引起的成年新生神经元祖细胞增殖和树突形态发生受损,同时改善记忆和焦虑样行为,而不影响肿瘤生长或顺铂的抗肿瘤活性。总的来说,我们的研究确定了 AR 信号作为一个关键途径,可以通过治疗靶向来预防顺铂引起的认知障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddf7/9282426/d35115840870/pnas.2206415119fig01.jpg

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