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生长抑素:将认知与阿尔茨海默病联系起来,以作为治疗靶点。

Somatostatin: Linking Cognition and Alzheimer Disease to Therapeutic Targeting.

机构信息

Pharmaceutical Sciences, School of Pharmacy, Southern Illinois University Edwardsville, Edwardsville, Illinois.

Pharmaceutical Sciences, School of Pharmacy, Southern Illinois University Edwardsville, Edwardsville, Illinois

出版信息

Pharmacol Rev. 2024 Oct 16;76(6):1291-1325. doi: 10.1124/pharmrev.124.001117.

DOI:10.1124/pharmrev.124.001117
PMID:39013601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11549939/
Abstract

Over 4 decades of research support the link between Alzheimer disease (AD) and somatostatin [somatotropin-releasing inhibitory factor (SRIF)]. SRIF and SRIF-expressing neurons play an essential role in brain function, modulating hippocampal activity and memory formation. Loss of SRIF and SRIF-expressing neurons in the brain rests at the center of a series of interdependent pathological events driven by amyloid- peptide (A), culminating in cognitive decline and dementia. The connection between the SRIF and AD further extends to the neuropsychiatric symptoms, seizure activity, and inflammation, whereas preclinical AD investigations show SRIF or SRIF receptor agonist administration capable of enhancing cognition. SRIF receptor subtype-4 activation in particular presents unique attributes, with the potential to mitigate learning and memory decline, reduce comorbid symptoms, and enhance enzymatic degradation of A in the brain. Here, we review the links between SRIF and AD along with the therapeutic implications. SIGNIFICANCE STATEMENT: Somatostatin and somatostatin-expressing neurons in the brain are extensively involved in cognition. Loss of somatostatin and somatostatin-expressing neurons in Alzheimer disease rests at the center of a series of interdependent pathological events contributing to cognitive decline and dementia. Targeting somatostatin-mediated processes has significant therapeutic potential for the treatment of Alzheimer disease.

摘要

四十多年的研究支持阿尔茨海默病(AD)与生长抑素[生长激素释放抑制因子(SRIF)]之间的联系。SRIF 和表达 SRIF 的神经元在大脑功能中发挥着重要作用,调节海马体的活动和记忆形成。大脑中 SRIF 和表达 SRIF 的神经元的丧失是一系列相互依存的病理事件的核心,这些事件由淀粉样肽(A)驱动,最终导致认知能力下降和痴呆。SRIF 与 AD 之间的联系进一步扩展到神经精神症状、癫痫活动和炎症,而临床前 AD 研究表明,SRIF 或 SRIF 受体激动剂的给药能够增强认知能力。特别是 SRIF 受体亚型 4 的激活具有独特的特性,具有减轻学习和记忆下降、减少共病症状以及增强大脑中 A 的酶降解的潜力。在这里,我们回顾了 SRIF 与 AD 之间的联系以及治疗意义。意义陈述:大脑中的生长抑素和表达生长抑素的神经元广泛参与认知。阿尔茨海默病中生长抑素和表达生长抑素的神经元的丧失是一系列相互依存的病理事件的核心,这些事件导致认知能力下降和痴呆。针对生长抑素介导的过程具有治疗阿尔茨海默病的巨大治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/80506a75f809/pharmrev.124.001117f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/01c11589b7aa/pharmrev.124.001117f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/1bfd6274a201/pharmrev.124.001117f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/4db1ce759291/pharmrev.124.001117f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/80506a75f809/pharmrev.124.001117f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/01c11589b7aa/pharmrev.124.001117f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/1bfd6274a201/pharmrev.124.001117f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/4db1ce759291/pharmrev.124.001117f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8d2/11549939/80506a75f809/pharmrev.124.001117f4.jpg

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