Effects of Methanol Leaf Extracts of Selected Plants on the Plasma Electrolytes Levels in Preeclamptic-Induced Wistar Rats

doi.org/10.26538/tjnpr/v5i10.26

Authors

  • Kenneth Atoe Department of Chemical Pathology, Edo State University Uzairue, Edo State, Nigeria
  • MacDonald Idu Phytomedicine and Drug Discovery Research Group, Department of Plant Biology and Biotechnology, University of Benin, Benin City, Nigeria

Keywords:

Preeclampsia, Wistar rats, Methanol leaf extracts, Electrolytes, Pregnancy, Hypertension

Abstract

Plants have always been used in medicine. Global research on plant medicinal efficacies has led to the development of plant-based medicines. Although their efficacy in the treatment of preeclampsia have not been shown. The study investigated the effects of methanol leaf extracts of Jatropha curcas, Alchornea cordifolia and  Secamone afzelii on the plasma electrolytes levels of preeclampticWistar rats. The rats were given Adriamycin (3.5 mg/kg) via a lateral caudal vein after mild ether anesthesia. Female rats were coupled with reproductive male rats for 4 days after 2 weeks. In the vaginal smear, the presence of spermatozoa in the first day of pregnancy was documented. After preeclampsia was observed, the rats were administered extracts (50, 100, and 200 mg/kg body weight) orally on a daily basis during the third trimester and postpartum period. Na, K, and Clplasma levels were estimated using an Automatic Electrolyte Analyzer, model BT-500 Plus; whereas Ca and Mg were analyzed by colorimetric method using standard kits. Results showed that in induced preeclampsia, sodium levels were 129.3 mmol/L in the third trimester; however, this level considerably increased to 136.3 – 170.5 mmol/L after administration of various dosages of the extracts. Calcium and magnesium levels were likewise increased (7.1 to 11.9 mg/dL and 1.05 to 2.53 mEq/L, respectively) in induced Wistar rats after extracts administration. The capacity for plant extracts to correct hyponatremia, hypocalcemia and hypomagnesemia during preeclampsia has thus been presented. 

Author Biography

Kenneth Atoe, Department of Chemical Pathology, Edo State University Uzairue, Edo State, Nigeria

Applied Environmental Biosciences and Public Health Research Group, Department of Microbiology, University of Benin, Benin City, Nigeria

Phytomedicine and Drug Discovery Research Group, Department of Plant Biology and Biotechnology, University of Benin, Benin City, Nigeria

 

References

Edeoga HO, Okwu DE, Mbaebie BO. Phytochemical constituents of some Nigerian medicinal plants. Afr J

Biotechn. 2005; 4(7):685-688.

Atawodi SE. Antioxidant potential of African medicinal plants. Afr J Biotech. 2005; 4(2):128-133.

Tabassum H, Al-Jameil N, Ali M, Aziz Khan F, Al-Rashed M. Status of serum electrolytes in preeclamptic pregnant

women of Riyadh, Saudi Arabia. Biomed Res. 2015; 26(2):219-224.

Wagner LK. Diagnosis and management of preeclampsia. Am Fam Physician. 2004; 70(12):2317-2324.

WHO. Maternal mortality. [Online]. 2019 [cited 2021 Sept 11]. Available from: https://www.who.int/news-room/fact-sheets/detail/maternal-mortality

Ray JG, Diamond P, Singh G. Brief overview of maternal triglycerides as a risk factor for preeclampsia. Br J ObstetGynaecol. 2006;113(4):379-386.

Krishna GG, Kapoor SC. Potassium depletion exacerbates essential hypertension. Ann Int Med. 1991; 115(2):77-83.

Faisal AR, Ali R, Maha MB, Tariq HK. Sodium imbalance in preeclampsia. Iraqi J Med Sci. 2009; 1:41-48.

O’Shaughnessy KM and Karet FE. Salt handling and hypertension. J Clin Invest. 2004; 113(8):1075-1081.

Iwamoto T and Kita S. Hypertension, Na+/Ca2+ exchanger, and Na+, K+-ATPase. Kidney Int. 2006; 69(12):2148-2154.

Whelton PK. Potassium and blood pressure. In: Izzo JL Jr, Black HR, eds. Hypertension primer. (3rd ed.). Dallas: American Heart Association/Council on High Blood Pressure Research. 2003; 280-282p.

Podjarny E, Bernheim JL, Rathaus M, Pomeranz A, Tobvin D, Shapira J, Bernheim J. Adriamycin nephropathy: a

model to study the effects of pregnancy on renal disease in rat. Am J Physiol. 1992; 263(4 Pt 2):F711-715.

Feng M and DiPetrillo K. Non-invasive Blood Pressure Measurement in Mice. Methods Mol Biol. 2009; 573:45-55.

Nipanal HV, Maurrya DK, Susmitha S, Ravindra PN. Analysis of Proteinuria Estimation Methods in Hypertensive Disorders of Pregnancy. J Obstet Gynaecol India. 2018; 68(6):452-455.

Rowell TE. Reproductive cycle of the talapoin monkey (Miopithecustalapoin) Folia Primatol. 1977; 28:188-202.

Yussif MN, Salih MR, Sami AZ, Mossa MM. Estimation of serum zinc, sodium and potassium in normotensive and

hypertensive primigravida pregnant women. Tikrit Med J. 2009; 15(1):13-18.

Tietz NW. Fundamentals of Clinical Chemistry. (3rd Ed.). W.B. Saunders, Philadelphia, USA. 1987. 720p.

Natelson S. Techniques of Clinical Chemistry. (3rd Ed.). Thomas C.C., Springfield, IL. 1971; 190p.

Elin RJ. Assessment of magnesium status. Clin Chem. 1987; 33(11):1965-1970.

Magee LA, Pels A, Helewa M, Rey E, von Dadelszen P, Hypertension Guideline C: Diagnosis, evaluation, and

management of the hypertensive disorders of pregnancy: executive summary. J Obstet Gynaecol Can. 2014; 36(5):416-441.

Gupta M and Roy N. Serum sodium and potassium levels in preeclampsia: a clinical study. Indian. J Med Biochem

; 22(2):105-107.

Darkwa EO, Antwi-Boasiako C, Djagbletey R, Owoo C, Obed S, Sottis D. Serum magnesium and calcium in preeclampsia: a comparative study at the Korle-Bu Teaching hospital, Ghana. Integr Blood Press Contr. 2017;10:9-15.

Darkwa EO, Djagbletey R, Antwi-Boasiako C, Aryee G,Sottie D, Akowuah A. Serum sodium and potassium levels in preeclampsia: a case-control study in a large tertiary hospital in Ghana. Cogent Med. 2017; 4(1):1-10.

Gordon ES, Chart JJ, Hagedorn D, Shipley EG. Mechanism of sodium retention in preeclamptic toxemia. Obstet Gynecol. 1954; 4(1):39-50.

Abubakar SM and Sule MS. Effect of oral administration of aqueous extract of Cassia occidentalis L. seeds on serum

electrolytes concentration in rats. Bayero J Pure Appl Sci. 2010; 3(1):183-187.

Anjum KS and Alka NS. Electrolyte Status in Preeclampsia. Online IntInterdiscip Res J. 2013; 3(1):30-36.

Khan MY, Naqvi SHA, Dahot MU. Relation of maternal serum electrolyte, traces elements and other biochemical parameters in third trimester of pregnancy. Sindh Univ Res J. 2011; 43(2):245-248.

Gallen IW, Rosa RM, Esparaz DY. On the mechanism of the effects of potassium restriction on blood pressure and

renal sodium retention. Am J Kidney Dis. 1998; 31(1):19-27.

Narayana SL, Rao RB, Namani S, Suleman Md. Variations in serum uric acid and serum magnesium levels in pre-eclamptic women. Int J Med Heal Res. 2018; 4(8):10-13.

Yamamoto M, Yamaguchi T, Yamauchi M, Yano S, Sugimoto T. Acute-onset hypomagnesemia-induced hypocalcemia caused by the refractoriness of bones and renal tubules to parathyroid hormone. J Bone Miner Metab. 2011; 29(6):752-755.

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Published

2021-10-01

How to Cite

Atoe, K., & Idu, M. (2021). Effects of Methanol Leaf Extracts of Selected Plants on the Plasma Electrolytes Levels in Preeclamptic-Induced Wistar Rats: doi.org/10.26538/tjnpr/v5i10.26. Tropical Journal of Natural Product Research (TJNPR), 5(10), 1863–1867. Retrieved from https://tjnpr.org/index.php/home/article/view/397