Department of Pharmacology and Toxicology, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS, 39216, USA.
Geroscience. 2021 Apr;43(2):1065-1067. doi: 10.1007/s11357-021-00357-7. Epub 2021 Mar 27.
Alzheimer's disease (AD) and Alzheimer's disease-related dementias (ADRD) are emerging global health care crises and are primarily found among aging, especially with diabetes and hypertension. However, treatments based on current understanding have not been effective. The importance of vascular contribution to AD/ADRD has been recommended by the NINDS and NIA to be a focused research area. A recent study identified that phosphatidylinositol 4,5-bisphosphate (PIP) or its analogs could reverse cerebral hypoperfusion at the neurovascular unit in AD mice. Although more studies are needed to validate if PIP analogs have sustained effects on CBF and can rescue cognitive impairment in AD/ADRD, and to elucidate and clarify whether targeting the retrograde (capillary-to-arteriole) pathway is beneficial to BBB function in AD/ADRD with poor CBF autoregulation, this finding provides exciting progress in understanding vascular contributions to AD/ADRD and suggests that reversal of cerebral hypoperfusion could be a novel therapeutic target for the treatment of AD/ADRD.
阿尔茨海默病(AD)和与阿尔茨海默病相关的痴呆症(ADRD)是正在出现的全球医疗保健危机,主要发生在老龄化人群中,尤其是伴有糖尿病和高血压的人群中。然而,基于现有认识的治疗方法并不有效。NINDS 和 NIA 建议将血管对 AD/ADRD 的贡献作为一个重点研究领域。最近的一项研究表明,磷脂酰肌醇 4,5-二磷酸(PIP)或其类似物可以逆转 AD 小鼠神经血管单元的脑低灌注。尽管还需要更多的研究来验证 PIP 类似物是否对 CBF 有持续作用,并能否挽救 AD/ADRD 中的认知障碍,以及阐明和澄清靶向逆行(从毛细血管到小动脉)途径是否有益于 CBF 自动调节不良的 AD/ADRD 中的 BBB 功能,但这一发现为理解血管对 AD/ADRD 的贡献提供了令人兴奋的进展,并表明逆转脑低灌注可能是治疗 AD/ADRD 的一个新的治疗靶点。