The kynurenine pathway; A new target for treating maternal features of preeclampsia?

被引:18
|
作者
Worton, Stephanie A. [1 ]
Greenwood, Susan L. [1 ]
Wareing, Mark [1 ]
Heazell, Alexander E. P. [1 ,2 ]
Myers, Jenny [1 ,2 ]
机构
[1] Univ Manchester, Fac Biol Med & Hlth, Maternal & Fetal Hlth Res Ctr, Manchester, Lancs, England
[2] Manchester Univ NHS Fdn Trust, St Marys Hosp, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
基金
英国医学研究理事会;
关键词
Preeclampsia; Kynurenine pathway; Vascular dysfunction; Immunoregulation; ARYL-HYDROCARBON RECEPTOR; INDOLEAMINE 2,3-DIOXYGENASE; QUINOLINIC ACID; TRYPTOPHAN-METABOLITES; OXIDATIVE STRESS; PREGNANCY; PLASMA; INFLAMMATION; SUPEROXIDE; INHIBITION;
D O I
10.1016/j.placenta.2019.04.007
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In preeclampsia, vasospasm, oxidative stress, endothelial dysfunction, and immune dysregulation are key mediators of maternal disease. A new time-of-disease treatment is needed with the potential to treat these areas of pathophysiology. A review of the literature has indicated that metabolites of the kynurenine pathway have the potential to; (i) induce vasorelaxation of resistance arteries and reduce blood pressure; (ii) exert antioxidant effects and reduce the effects of poly-ADP ribose polymerase activation (iii) prevent endothelial dysfunction and promote endothelial nitric oxide production; (iv) cause T cell differentiation into tolerogenic regulatory T cells and induce apoptosis of pro-inflammatory Th1 cells. This has led to the hypothesis that increasing Kynurenine pathway activity may offer a new treatment strategy for preeclampsia.
引用
收藏
页码:44 / 49
页数:6
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