Antiplasmodial Activity and Toxicological Study of Two Anti-Malarial Herbal Medicines, Balm of Gilead (BOG) and Prolife Herbal Medicine (Prolife) in Infected Albino Mice

Authors

  • Esther Anya Orji Department of Animal and Environmental Biology, University of Port Harcourt, Choba, Rivers State, Nigeria
  • Chinwe Nwadiuto Eze Department of Animal and Environmental Biology, University of Port Harcourt, Choba, Rivers State, Nigeria

DOI:

https://doi.org/10.14738/bjhmr.105.15274

Keywords:

Antimalarial, Toxicity, Malaria

Abstract

The treatment of malaria is becoming more challenging due to the problem of resistance and poverty. The present study investigated the antimalarial activity and toxicity of two herbal medicines: Balm of Gilead and Prolife antimalarial drugs. Malaria infection was established by inoculating mice with 1 ×107 parasitized blood (Plasmodium berghei) and treatment was done by a single dose of 100mg/kg herbal medicines given once a day in a curative (Rane's test) and prophylactic tests. The results were compared with standardized medicines; Chloroquine/Fansider and Lonart. Histology of liver, kidney and spleen was conducted after the treatment period. On Day14 post treatment, BOG and Prolife had average parasitemia level of 3.63 ±0.80 and 3.88 ±0.87 and average parasite suppression of 73.5% and 63.4% respectively. In the prophylactic treatment, BOG and Prolife had average parasitemia level 7.01 ± 0.07 and 10.92 ± 0.02 respectively.  The negative control showed increased level of parasitemia at Day 14.     The results showed that BOG and PROLIFE exhibited considerable antimalarial potential. On the other hand, the histology results showed mild distortion on the liver and spleen but safe to the kidney. Therefore, in as much as these drugs can cure and prevent malaria, they can also be a potential health threat if not taken properly with caution. I suggest regulatory bodies and pharmaceutical companies should under study the active ingredients for preparations of these anti-malaria drugs.

References

Nguta, J., Mbaria, J., Gathumbi, P., Gakuya, D., Kabasa, J. & Kiama, S. (2013). Brine shrimp toxicity and antimalarial activity of some plants traditionally used in treatment of malaria in Msambweni district of Kenya. Journal of ethnopharmacology, 148(2): 988-992.

Joanne, B., Michel, F., & Joelle, Q. (2009). Antimalarial compounds isolated from plants used in traditional medicine. Journal of Pharmacy and Pharmacology, 61:1401–1433.

WHO (2019). Malaria fact sheet Geneva Author Retrieved from https://www.who.int/newsroom/factsheets/detail/malaria.

World Health Organization (2021). World Malaria Report 2021

Abeku TA (2007). Response to malaria epidemics in Africa. Emerging infectious disease 13(5):68

Offianan, A. T., Tuo, K., Beourou, S., Koffi, D., Djaman, A. J. & Coulibaly, A. (2018). Antiplasmodial activity of Diospyros monbuttensis and Newbouldia laevis, two Ivorian medicinal plants. Res. J. Parasitol., 13: 57-64

Kumar A, Ellis P, Arabi Y, Roberts D, Light B, Parrillo JE, Dodek P, Wood G, Kumar A, Simon D, Peters C, Ahsan M, Chateau D; (2009). Cooperative Antimicrobial Therapy of Septic Shock Database Research Group. Initiation of inappropriate antimicrobial therapy results in a fivefold reduction of survival in human septic shock. Chest. ;136(5):1237-1248. doi: 10.1378/chest.09-0087.

Lau, A., Holmes, M.J., Woo, S. & Koh, H. (2003). Analysis of adulterants in traditional herbal medicinal product using liquid chromatography mass spectroscopy. Journal of Pharm. Bio A 31:401-406.

Waako, P., Gumede, B., Smith, P., Folb, P. (2005). The in vitro and in vivo anti- malarial activity of Cardiospermum halicacabum L. and Momordica foetida Schumch Et. Thonn. J Ethnopharmacol. 99:137–43.

Cheesbrough, M. (2010). District Laboratory practice in Tropical Countries. Tropical Health Technology Cambridge University Press.

Okpe, O., Habila, N., Ikwebe, J., Vincent, A., Okoduwa, R. & Omiagocho, T. (2016). Antimalarial Potential of Carica papaya and Vernonia amygdalina in Mice Infected with Plasmodium berghei. Journal of Tropical Medicine.

Khosla, P., Bhanwra, S., Singh, J., Seth, S. & Srivastava, R. K. (2000). A study of Hypoglycemic effects of Azadirachta indica (Neem) in normaland alloxan diabetic rabbits. Indian journal Physiol Pharmacol. 11: 123-125

Oseni L.A. and Akwetey G.M. (2012). An in-vivo evaluation of antiplasmodial activity of aqueous and ethanolic leaf extracts of Azadirachta indica in Plasmodium berghei infected balb/c mice. Vol. 3 (5) 1406-

Razis, R. A. F., Ibrahim, M. D., Kntayya, S.B. (2014). Health benefits of Moringa oleifera. Asian Pac J Cancer Prev. 15(20):8571-6

Dondee, K., Bootprom, P., Saiphet, B., Borkaew, P., Klubsri, C., & Somsak, V. (2016). Antimalarial Activities of Moringa oleifera Leaf Extract Against Plasmodium berghei ANKA Infection in ICR Mice. International Journal of Innovative Research in Medical Sciences (IJIRMS).1(5), 194 -201

Ugwoke, C., Anze, S., Nweze, A. (2017). Pharamacognostic evaluation of the leaf of Antians toxicaria (Family Moraceae). International Journal of Pharmacology. 1(2): 65-77.

Hano, Y., Mitsui, P. & Nomura, T. (1990). Seven prenylphenols, antiarones C, D, E, F, G, H and 1 from the root bark of Antiaris toxicaria lesch. Heterocycles 31: 1315-1323.

Aibinu, I., Adenipekun, T., Adelowotan, T., Ogunsanya, T. & Odugbemi, T. (2006). Evaluation of the antimicrobial properties of different parts of Citrus aurantifolia (lime fruit) as used locally. Afr J Tradit Complement Altern Med. 4: 185-90.

Tchoumbougnang, F., Zollo, P. H., Dagne, E. & Mekonnen, Y. (2005). In vivo antimalarial activity of essential oils from Cymbopogon citratus and Ocimum gratissimum on mice infected with Plasmodium berghei. Planta Med 71:20-3.

Munoz, V., Sauvain, M., Bourdy, G., Callapa, J., Bergeron, S., Rojas, I. (2000). A search for natural bioactive compounds in Bolivia through a multidisciplinary approach. Part I. Evaluation of the antimalarial activity of plants used by the Chacobo Indians. J Ethnopharmacol. 69:127–37.

Mohammed, T., Erko, B., & Giday, M. (2014). Evaluation of antimalarial activity of leaves of Acokanthera schimperi and Croton macrostachyus against Plasmodium berghei in Swiss albino mice. BMC Complement Altern Med.14:314

Adewole, E. O., Salami, A.T. & Taiwo, V.O, (2010). Anti plasmodial and toxicological effects of methanolic bark extract of Chrysophyllum albidum in albino mice. Journal of Physiology and Pathophysiology. Vol 1(1). Pp 1-9. URL: http://dx.doi.org/10.14738/bjhmr.105.15274. 89

Bantie, L., Assefa, S., Teklehaimanot, T. & Engidawork, E. (2014). In vivo antimalarial activity of the crude leaf extract and solvent fractions of Croton macrostachyus Hocsht. (Euphorbiaceae) against Plasmodium berghei in mice. BMC Complement Altern Med. 14:79.

Chinchilla, M., Guerrero, O., Abarca, G., Barrios, M., Castro, O. (1998). An in vivo model to study the antimalaria capacity of plant extracts. Rev Biol Trop. 46:1–7.

Cederbaum, A. I. (2015). Molecular mechanisms of the microsomal mixed function oxidases and biological and pathological implications. Redox Biology, vol. 4, pp. 60–73

Dikibo, E., Okpe, A. C., Turray, A. A., Onodagu, B. O., Ogbodo, L. A. and Oyadonghan G. P. (2012). The effect of carica papays seeds on the histology of the liver in wister rats. International Journal of Herbs and Pharamacological Research IJHPE 1(2): 48-54.

Downloads

Published

2023-09-10

How to Cite

Orji, E. A., & Eze, C. N. (2023). Antiplasmodial Activity and Toxicological Study of Two Anti-Malarial Herbal Medicines, Balm of Gilead (BOG) and Prolife Herbal Medicine (Prolife) in Infected Albino Mice. British Journal of Healthcare and Medical Research, 10(5), 79–90. https://doi.org/10.14738/bjhmr.105.15274