Background to the Study: Pathophysiology of Plasmodium infection and the metabolism of the phytochemicals of raw liquid extract of Vernonia amygdalina used in the traditional treatment of Plasmodium spp infection in Saki-East Local Government area of Oyo state -Nigeria involve the hepatocytes, which could bring about biochemical alterations in the plasma level of albumin, fibrinogen, Lactate dehydrogenase (LDH) and Total Bile Acids (TBA). Aim and Objective: This work was designed to determine the effect of the raw extract of Vernonia amygdalina used in the treatment of Plasmodium spp infection on acute phase protein (albumin, fibrinogen), Total bile acids and Lactate dehydrogenase. Materials and Method: Forty five 45 (72.6%) that were HIV, HBsAg and anti-HCV seronagative female-23 (51.1%); male-22 (48.9%) aged 21-48 years were recruited and studied out of the sixty two (62) patients infected with Plasmodium spp based on the exclusion and inclusion criteria from 5 herbal homes in Saki-East Local government area of Oyo-state-Nigeria. Giemsa-thick film staining technique was used for Plasmodium detection including estimation of plasmodium parasite density and Viral immunochemical serology for anti-HIV, anti-HCV and HBsAg was carried out in the 62 subjects initially recruited was determined by ELIZA and Immunoblotting. These tests were also employed in recruiting the normal control subjects (n=50). Plasma albumin, fibrinogen, Total Bile Acids and Lactate dehydrogenase were analyzed in the control and Plasmodium infected subjects before and after treatment with the raw extract of Vernonia amygdalina. Results: There was a significantly lower mean values of fibrinogen, LDH, Parasite density in the control Plasmodium non-infected subjects (264±10.6 mg/dl; 253 ±13.1 U/L; 0 µL) than the values (438±10.1 mg/dl; 302±18 U/L; 490±10.0 /µL) obtained in the plasmodium infected subjects before treatment with p<0.05. There was also a significantly lower mean values of fibrinogen and parasite density in the control Plasmodium non-infected subjects (264±10.6 mg/dl; 0/µL) than the values obtained in the Plasmodium infected patients after treatment with the extract (358±10.2 mg/dl; 205±15/µL) with p<0.05. However there was a significantly higher mean values of Fibrinogen, TBA, LDH, and Parasite density of 438±10.1 mg/dl, 13±1.8 µmol/L, 302±18 U/L and 490±10/µL respectively in the Plasmodium infected subjects before treatment than the values of the these parameters obtained in the same subjects after the treatment (358±10.2 mg/dl; 10.1±1.5 µmol/L; 264±12 U/L; 205±15/µL) with p<0.05. The results obtained also showed a lower significant difference in the plasma value of albumin in the Plasmodium infected subjects before treatment (3.6±0.3 g/dl) than the value obtained in the same subjects after treatment (4.1±0.2 g/dl) with p< 0.05. The immunochemical status of the Plasmodium infected patients revealed: 17.7% (11) out of the 62 Plasmodium infected patients were tested positive to HIV, HBsAg or anti-HCV which include: 9.7% (6) HIV, 4.8% (3) HBV and 3.23% (2) HCV while 8.1% (5) of them were detected to be alcoholics and 1.6% (1) was found to be under analgesic therapy using paracetamol. Conclusion: There was a significant biochemical alterations in the concentration of plasma acute phase proteins (fibrinogen, albumin), Lactate dehydrogenase, Total Bile acids and parasite density in Plasmodium infected patients before the traditional treatment with extract of Vernonia amygdalina which was restored almost to normal after the treatment supporting the use of Vernonia amygdalina as an effective anti-plasmodia agent. The result obtained also revealed the immunochemical status of the Plasmodium infected patients as: 17.7% (11) out of the 62 Plasmodium infected patients were tested positive to HIV, HBsAg or anti-HCV which include: 9.7% (6) HIV, 4.8% (3) HBV and 3.2% (2) HCV.
| [1] | Ugwoke CEC, Nzekwe U, Ameh GI. Phytochemical constituents and ethnobotany of the leaf extract of bitter leaf (Vernonia amygdalina) Del. Journal of Pharmaceutical and Allied Sciences; 2010; Vol 7, No 3. |
| [2] | Udensi, E. A., Ijeh, I. I., Ogbonna, U. Effect of traditional processing on the phytochemical and nutrient composition of some local Nigerian leafy vegetables. Journal of Science and Technology, 2002; 8, 37-40. |
| [3] | Ejoh, R.A., Nkonga, D.V., Innocent, G., Moses, C. Nutritional components of some nonconventional leafy vegetables consumed in Cameroon. Pakistan Journal of Nutrition. 2007; 6, 712-7.View Article |
| [4] | Eleyinmi, A.F., Sporns, P., Bressler, D.C. Nutritional compostion of Gongronemalatifolium and Vernonia amygdalina. Nutrition and Food Sciences, 2008: 38, 99-100.View Article |
| [5] | Igile, G. O., Olezek, W., Jurzysata, M., Burda, S., Fafunso, M., Fasanmade, A.A.. Flavonoids from Vernonia amygdalina and their antioxidant activities. Journal of Agricultrual and Food Chemistry (USA). 1994: 42 (11), 2445-2448.View Article |
| [6] | Tona L., Cimanga, R. K., Mesia, K., Musuamba, C. T., Bruyne, T., Apers, S., Hermans, N., Van Miret, S., Pieters, L., Totte, J., Vlietnk, A. J. In vitro antiplasmodial activity of extracts and fractions of seven medicinal plants used in Democratic Republic of Congo. Journal of Ethnopharmacology, 2004: 93, 27-32.View Article PubMed |
| [7] | Farombi, E. O. African indigenous plants with chemotherapeutic potentials and biotechnological approach to the production of bioactive prophylactic agents. African Journal of Biotechnology. 2003: 2, 662-7. |
| [8] | Vattem, D.A., Ghaedian, R. and Shetty, K. Benefits of berries through phenolic antioxidant enrichment focus on cranberry. Asia Pac. Jrn of Clinical Nutrition. 2005: 14 (2):120-130. PubMed |
| [9] | Souza, S.M.C., Aquino, L.C. et al., Anti_inflammatory and anti-ulcer properties of tannins from Myracrodiruonurundeuva Allemao (Anacardiacea) in rodents. Phytotherapy Res. 2006: 21 (3) 220-225.View Article PubMed |
| [10] | Reddy, M.K., Gupta, S.K., Jacob, M.R., Khan, S.I. Antioxidants, anti-malarial and antimicrobial activities of tannin-rich fractions, ellagitannins and phenolic acids from Punicagranatum L. Planta Medica. 2007: 73 (5): 461-467.View Article PubMed |
| [11] | Silva, R.E., Amorim, M.A., Melo, M.R., Henrique, M.C., Nunomura, S.M., Costa, M.R., Andrade, N.V.F., Costa, D.S., Dantas, G., Lavrado, J. et al., Comparative in-vivo and in-vitro antimalarial activity of the indole alkaloids ellipticine, olivacine, cryptolepine and a synthetic cryptolepine analog. Phytomedicine. 2012: 20 (1): 71-76.View Article PubMed |
| [12] | Yakubu, M.T., Adesokan, A.A. and Akanji, M.A. Biochemical changes in the liver, kidney and serum of rats following chronic administration of cimetidine. African Journal of Biomedical Research. 2006: 9:213-218. |
| [13] | Aceeti, C.N. Methods Industria Farmaceutica Cantabria, Arequipa I. Madrid-Spain Experimental and Clinical Pharmacology. 2006: 28 (3):157-160. |
| [14] | Ovenden, S.P., Cobbe, M., Kissel, R. et al., Phenolic glycosides with antimalarial activity from Greoillea (Poorinda Queen) Journal of Natural Products. 2011: 74 (1): 14-48.View Article PubMed |
| [15] | Yamamoto, A.S. and Gaynor, P.O. Therapeutic Potential of Inhibition of the NF-KB Pathway in the treatment of the infalmmation and cancer. Journal of Clinical Investigation. 2006: 107 (2): 135.View Article PubMed |
| [16] | Choi, R.J., Ngoc, T.M., Bae, K., Cho, H.J., Kim, D.D., Chun,J., Khan, S. and Kim, Y.S. Anti-inflammatory properties of anthraquinones and their relationship with the regulation of P-glycoprotein function and expression. European Journal of Plasma Science. 2012: 48 (1-2): 272-281.View Article PubMed |
| [17] | Gherraf, N., Zellagui, A., Mohammed, N.S. et al., Triterpens from Euphorbia rigida. Pharmacognosy Research. 2010: 2 (3): 159-62.View Article PubMed |
| [18] | Da silva, G.N.S., Nicole, R.G.M., Desiree, C.S., Cruz, N.C. De moraes, M.S. Nakabashi, M.C.G. Gosmann, G., Garcia, R.S.C and Gricatto, C.B. Two series of new semisynthesictriterpenederivatives: differences in antimalarial activity, cytotoxicity and mechanism of action. Malaria journal. 2013: 12: 89-96. PubMed PubMed |
| [19] | Osthind, R.E., Racette, S.B. and Stenson, W.F. Inhibition of cholesterol absorption by phytosterol-replete wheat germ compared with phytosterol-depleted wheat germ. American Journal of Clinical Nutrition. 2003: 77 (6): 1385-1589. |
| [20] | Herpers B L, Endeman H, de Jong B A W, de Jongh B M, Grutters J C, Biesma D H, and van Velzen-Blad H. Acute-phase responsiveness of mannose-binding lectin in community-acquired pneumonia is highly dependent upon MBL2 genotypes. ClinExp Immunol. 2009: Jun; 156 (3): 488-94. |
| [21] | Abbas, A., Lichtman, A., &Pillai, S. Basic immunology Functions and Disorders of the Immune System (4th ed., p. 40). Philadelphia, PA: Saunders/Elsevier. 2012. |
| [22] | Russell DW. “The enzymes, regulation, and genetics of bile acid synthesis”. Annu. Rev. Biochem. 2003: 72: 137-74.View Article PubMed |
| [23] | Chiang JY. “Bile acids: regulation of synthesis”. J. Lipid Res. 2009:50 (10): 1955-66. PMC 2739756.View Article PubMed |
| [24] | Selwood T, Jaffe EK. “Dynamic dissociating homo-oligomers and the control of protein function”. Arch. Biochem. Biophys. 2012:519 (2): 131-43. PMC 3298769.View Article PubMed |
| [25] | Spriet LL, Howlett RA, Heigenhauser GJ. “An enzymatic approach to lactate production in human skeletal muscle during exercise.” Med Sci Sports Exerc 2000:32 (4): 756-63.View Article PubMed |
| [26] | Summer matter S, Santos G, Pérez-Schindler J, Handschin C. “Skeletal muscle PGC-1α controls whole-body lactate homeostasis through estrogen-related receptor α-dependent activation of LDH B and repression of LDH A.”. Proc Natl Acad Sci U S A 2013: 110 (21): 8738-43.View Article PubMed |
| [27] | Cheesbrough, Monica. District Laboratory practice in tropical Countries part 1. 2002: Cambridge low-price edition. Cambridge University Press. |
| [28] | Greenwood BM, Armstrong JRM. Comparison of two simple methods for determining malaria parasite density. Transactions of the Royal Society of Tropical Medicine and Hygiene.; 1991:85: 186-188.View Article |
| [29] | Omoigberale AI1, Abiodun PO, Famodu AA. Fibrinolytic activity in children with Plasmodium falciparum malaria. East Afr Med J. 2005: Feb; 82 (2): 103-5. |
| [30] | Yeo TW, Lampah DA, Gitawati R, Tjitra E, Kenangalem E, McNeil YR, Darcy CJ, Granger DJ, Weinberg JB, Lopansri BK, Price RN, Duffull SB, Celermajer DS, Anstey NM. Recovery of endothelial function in severe falciparum malaria: relationship with improvement in plasma L-arginine and blood lactate concentrations. J Infect Dis, 2008:198:602-608. PubMed Abstract | Publisher Full Text |PubMed Central Full Text Ladhaniet al., 2010 |
| [31] | I H Garba, G AUbom. Total serum lactate dehydrogenasenactivity in acute Plasmodium falciparum malaria infection. Singapore Med J. 2005: 46 (11): 632. PubMed |
| [32] | Van Wolfswinkel ME, Hesselink DA, Zietse R, Hoorn EJ, van Genderen PJJ. Hyponatraemia in imported malaria is common and associated with diseaseseverity. 2010: MalarJ, 9: 140.View Article PubMed |
| [33] | MacPherson GG, Warrell MJ, White NJ, Looareesuwan S, Warrell DA. Human cerebral malaria. A quantitative ultrastructural analysis of parasitized erythrocyte sequestration. Am J Pathol. 1985: 119:385-401. PubMed PubMed |
| [34] | Prommano O, Chaisri U, Turner GD, Wilairatana P, Ferguson DJ, Viriyavejakul P, White NJ, Pongponratn E. A quantitative ultrastructural study of the liver and the spleen in fatal falciparum malaria. Southeast Asian J Trop Med Public Health. 2005: 36: 1359-1370. PubMed |
| [35] | Christina C Chang, Megan Crane, and Sharon R Lewin. HIV and Coinfections. Immunol. Rev. 2013: 254 (1); 114-142. |
| [36] | Mathew Folaranmi OLANIYAN; Elizabeth Moyinoluwa BABATUNDE American Journal of Biomedical Research., 2014: 2 (3), 47-51.View Article |
| [37] | Ladhani S, Garbash M, Whitty CJ, Chiodini PL, Aibara RJ, Riordan FA, Shingadia D. Prospective, national clinical and epidemiologic study on imported childhood malaria in the United Kingdom and the Republic of Ireland. Pediatr Infect DisJ, 2010: 29: 434438. Pub Med Abstract | Publisher Full TextView Article PubMed |
| [38] | Page RC, Schroeder HE. "Pathogenesis of inflammatory periodontal disease. A summary of current work". Lab. Invest.; 1976: 34 (3): 235-49. PubMed |