Table 4.
Reference | Type of Study | Dose | Duration | Maternal Outcomes | Embryonic, Fetal and Neonatal Outcomes |
---|---|---|---|---|---|
Li et al., 2020 [12] | Experimental (rats subjected to preeclampsia model) | The authors did not inform the dose of treatment. | The authors did not inform the duration of treatment. | ↓ Systolic blood pressure; ↓ Proteinuria. |
Reversed imbalance of angiogenic factors production in the placenta; ↓ Placental growth factor; ↓ Placental expression of TNF-α, IL-6, and MCP-1 levels; ↓ Placental MDA; ↑ Placenta weight; ↓ Reabsorbed fetuses %; ↑ Pups weight; ↑ Placenta weight. |
Sun et al., 2020 [68] | Experimental (rats subjected to gestational hypertension) | 10 mg/kg, 20 mg/kg, or 50 mg/kg. | From gestational day 14 to gestational day 21. | ↓ Systolic and diastolic blood pressure; ↓ Plasma level of ET-1, sFLT1; ↑ Plasma level of VEGF; ↓ Plasma levels of TNF-α and IL-6, and ↑ IL-10. |
↓ ET-1, ETAR expression in placenta tissue; ↑ Fetal weight; Did not change placental weight; ↑ Fetal weight/ Placenta weight; ↓ Reabsorbed fetuses %. |
Tanir et al., 2005 [23] | Experimental (rats subjected to preeclampsia model) | 10 mg/kg | Single administration at gestational day 17. | Did not change blood pressure;↓ Plasma MDA levels; ↓ Erythrocyte CAT and SOD levels; ↓ Proteinuria. |
Did not change the birth weight of pups; ↑ Neonatal survival (higher percentages of liveborn pups and lower rates of dead pups). |
Yang et al., 2019 [67] | Experimental (rats subjected to preeclampsia model) | 2 mg/kg | From gestational day 4 to gestational day 19. | ↓ Proteinuria; ↓ Plasma MDA levels; Did not change TNF-α; ↓ Plasma levels of IL-6. |
Did not change placental MDA; Did not change placental expression of TNF-α and IL-6; Did not change relative mRNA expression of uterus VEGF and sFlt-1. |