Abstract

BackgroundPreeclampsia (PE) is a serious maternal complication during pregnancy. Associated arterial stiffness in PE patients leads to increased risks of cardiovascular diseases later in life. Cholesterol efflux capacity, especially ATP binding cassette transporter A1 (ABCA1) dependent capacity, has been proposed to be a likely mediator of arterial stiffness. In the present study, we aimed to evaluate the effect of an apolipoprotein A1 mimetic peptide ATI-5261 on arterial stiffness in a mouse model of PE.MethodsPregnant COMT−/− mice were randomized to receive vehicle or ATI-5261 (30 mg/kg per day) via subcutaneous injection from gestational days (GD) 10.5 to GD 18.5 or to 10 days postpartum. Pregnant C57BL/6 J mice received vehicle during paralleled periods were served as normal controls.ResultsCOMT−/− mice displayed maternal hypertension and proteinuria during pregnancy. Carotid–femoral pulse wave velocity (PWV) was increased at GD 18.5 and 10 days postpartum. ATI-5261 treatment in COMT−/− mice significantly reduced PWV and partially normalized impaired ex vivo vascular function at late pregnancy and early postpartum. ATI-5261 treatment also increased serum ABCA1 concentrations and cholesterol efflux capacity, as well as ABCA1 expressions in the placenta. Pup weights, crown to rump lengths and abdominal circumferences were reduced in COMT−/− mice. Treatment with ATI-5261 did not alter these fetal measurements but significantly reduced placental weights and increased fetal to placental ratios in COMT−/− mice.ConclusionATI-5261 reversed arterial stiffness at late pregnancy and early postpartum in a COMT−/− mouse model of PE and may be a potential therapy for arterial stiffness associated with PE.

Highlights

  • Preeclampsia (PE) is a serious maternal complication during pregnancy

  • Female homozygous catechol-O-methyl transferase knockout (COMT−/−; Cyagen Biosciences Inc.) mice and C57BL/6 J mice (Jackson laboratories) aged 8 to 12 weeks were housed under standard conditions and maintained at 22 °C with a 12-h light/dark cycle and with ad-libitum access to food and water

  • Systolic blood pressure in vehicle treated Catechol-O-methyl transferase (COMT)−/− mice was significantly increased at gestational days (GD) 18.5 and the increased blood pressure returned to nonpregnant levels at 10 days after delivery; systolic blood pressure in vehicle treated C57BL/6 J mice was significantly decreased at GD 18.5; systolic blood pressure in ATI-5261 treated COMT−/− mice was unaltered during pregnancy

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Summary

Introduction

Associated arterial stiffness in PE patients leads to increased risks of cardiovascular diseases later in life. ATI-5261 treatment in COMT−/− mice significantly reduced PWV and partially normalized impaired ex vivo vascular function at late pregnancy and early postpartum. Treatment with ATI-5261 did not alter these fetal measurements but significantly reduced placental weights and increased fetal to placental ratios in COMT−/− mice. Conclusion: ATI-5261 reversed arterial stiffness at late pregnancy and early postpartum in a COMT−/− mouse model of PE and may be a potential therapy for arterial stiffness associated with PE. Women with PE are at increased risks of cardiovascular diseases later in life, which may be associated with persisting endothelial, cardiovascular, and metabolic dysfunction, as well as increased arterial stiffness following preeclamptic pregnancies [3,4,5]. The initial and rate-limiting step of cholesterol efflux is the transport of cellular free cholesterol to

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