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DOI 10.1161/hypertensionaha.123.22633

Медицинская библиотека · Hypertension (Dallas, Tex. : 1979) · 2024

Placental Methylglyoxal in Preeclampsia: Vascular and Biomarker Implications.

Vangrieken Philippe, Al-Nasiry Salwan, Remels Alex H V, Schiffers Paul M H, Janssen Emma, Nass Stefanie, Scheijen Jean L J M, Spaanderman Marc E A, Schalkwijk Casper G

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Preeclampsia is a multifaceted syndrome that includes maternal vascular dysfunction. We hypothesize that increased placental glycolysis and hypoxia in preeclampsia lead to increased levels of methylglyoxal (MGO), consequently causing vascular dysfunction.

METHODS

Plasma samples and placentas were collected from uncomplicated and preeclampsia pregnancies. Uncomplicated placentas and trophoblast cells (BeWo) were exposed to hypoxia. The reactive dicarbonyl MGO and advanced glycation end products (Nε-(carboxymethyl)lysine [CML], Nε-(carboxyethyl)lysine [CEL], and MGO-derived hydroimidazolone [MG-H]) were quantified using liquid chromatography-tandem mass spectrometry. The activity of GLO1 (glyoxalase-1), that is, the enzyme detoxifying MGO, was measured. The impact of MGO on vascular function was evaluated using wire/pressure myography. The therapeutic potential of the MGO-quencher quercetin and mitochondrial-specific antioxidant mitoquinone mesylate (MitoQ) was explored.

RESULTS

MGO, CML, CEL, and MG-H2 levels were elevated in preeclampsia-placentas (+36%, +36%, +25%, and +22%, respectively). Reduced GLO1 activity was observed in preeclampsia-placentas (-12%) and hypoxia-exposed placentas (-16%). Hypoxia-induced MGO accumulation in placentas was mitigated by the MGO-quencher quercetin. Trophoblast cells were identified as the primary source of MGO. Reduced GLO1 activity was also observed in hypoxia-exposed BeWo cells (-26%). Maternal plasma concentrations of CML and the MGO-derived MG-H1 increased as early as 12 weeks of gestation (+16% and +17%, respectively). MGO impaired endothelial barrier function, an effect mitigated by MitoQ, and heightened vascular responsiveness to thromboxane A2.

CONCLUSIONS

This study reveals the accumulation of placental MGO in preeclampsia and upon exposure to hypoxia, demonstrates how MGO can contribute to vascular impairment, and highlights plasma CML and MG-H1 levels as promising early biomarkers for preeclampsia.

Для цитирования: Vangrieken Philippe, Al-Nasiry Salwan, Remels Alex H V, Schiffers Paul M H, Janssen Emma, Nass Stefanie, Scheijen Jean L J M, Spaanderman Marc E A, Schalkwijk Casper G. Placental Methylglyoxal in Preeclampsia: Vascular and Biomarker Implications.. Hypertension (Dallas, Tex. : 1979). 2024. DOI: 10.1161/hypertensionaha.123.22633.

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