A Review of Oxylipins in Alzheimer's Disease and Related Dementias (ADRD): Potential Therapeutic Targets for the Modulation of Vascular Tone and Inflammation

被引:15
作者
Shinto, Lynne H. [1 ]
Raber, Jacob [1 ,2 ,3 ]
Mishra, Anusha [1 ,4 ]
Roese, Natalie [1 ]
Silbert, Lisa C. [1 ,5 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Neurol, 3181 SW Sam Jackson Pk Rd,CR120, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Div Neurosci, ONPRC, Portland, OR 97239 USA
[3] Oregon Hlth & Sci Univ, Dept Radiat Med, Div Neurosci, ONPRC, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Jungers Ctr Neurosci Res, Portland, OR 97239 USA
[5] Vet Affairs Med Ctr, Portland, OR 97239 USA
基金
美国国家卫生研究院;
关键词
review; oxylipin; fatty acids; vascular dementia; Alzheimer's disease; SOLUBLE EPOXIDE HYDROLASE; ALPHA-LINOLENIC ACID; LONG-CHAIN OMEGA-3-FATTY-ACIDS; MATTER HYPERINTENSITY VOLUME; POLYUNSATURATED FATTY-ACIDS; DOCOSAHEXAENOIC ACID; BLOOD-PRESSURE; CARDIOVASCULAR-DISEASE; EICOSAPENTAENOIC ACID; GUT MICROBIOTA;
D O I
10.3390/metabo12090826
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is now a convincing body of evidence from observational studies that the majority of modifiable Alzheimer's disease and related dementia (ADRD) risk factors are vascular in nature. In addition, the co-existence of cerebrovascular disease with AD is more common than AD alone, and conditions resulting in brain ischemia likely promote detrimental effects of AD pathology. Oxylipins are a class of bioactive lipid mediators derived from the oxidation of long-chain polyunsaturated fatty acids (PUFAs) which act as modulators of both vascular tone and inflammation. In vascular cognitive impairment (VCI), there is emerging evidence that oxylipins may have both protective and detrimental effects on brain structure, cognitive performance, and disease progression. In this review, we focus on oxylipin relationships with vascular and inflammatory risk factors in human studies and animal models pertinent to ADRD. In addition, we discuss future research directions with the potential to impact the trajectory of ADRD risk and disease progression.
引用
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页数:25
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