The Effects of Aqueous Leaf Extract of Tridax Procumbens on the Haematological and Serum Biochemical Parameters of Wistar Albino Rats

  • Olukunle O. J.
  • Abatan O. M.

Abstract

The effects of different doses of aqueous leaf extract of Tridax procumbens were evaluated in Wistar albino rats. The leaf extract of T. procumbens was administered orally for 14 days. Changes in the haematological and serum biochemical parameters were observed as indices of toxicity of the extract. The 100 and 400 mg/kg doses of the leaf extract of T. procumbens caused significant (P<0.05) decrease in the levels of the packed cell volume (PCV) (21.5±2.5 versus 37.3±1.5), and (20*±1.5 versus 37.3±1.5)%, respectively. The 100 and 400 mg/kg doses also significantly reduced haemoglobin concentration (Hb), (7.1*±2.4 versus 12±0.4)g/dl and (6.4*±12 versus 12±0.4)g/dl, respectively and red blood cell counts (RBC) (1.82*±0.11 versus 5.7±0.4) and (2.7±5.7 versus 5.7±0.4) respectively. These changes are reflected in the significant increase in the mean corpuscular volume for rats in the 100 and 400 mg/kg, suggesting that the aqueous crude extract of T. procumbens  adversely affected  the erythron of rats and may cause a normocytic normochromic anaemia in the animals consuming them. This study also revealed that the extract  caused statistically significant (P<0.05) decrease in the level of circulating lymphocyte but significant (P<0.05) increase in the level of circulating neutrophil (41*±2.6 versus 25.7±3.9) at the doses of 400mg/kg b.w treatment group. The lymphopaenia (i.e. reduction in lymphocyte count) observed may indicate immunosuppression and the neutrophilia observed may imply inflammatory reactions and defense against microbial infections. The aqueous crude extract of T. procumbens leaf also caused a statistically significant (P<0.05) increase in the level of serum aspartate aminotransferase (AST) (2.81*±4.1 versus 30.3±14) and (27.8*±6 versus 220.3±14) respectively at two different dosages, i.e., at 100 and 400 mg/kg b.w. The elevation observed in the serum AST values may indicate haemolysis, which implies that the aqueous extract of T. procumbens caused anaemia in Wistar Albino rats and therefore has toxic potential.

References

Abad, M.I., Bermejo, P., Carretero E., Martinez- Acitores C., Noguera B., Villar A. 1996. Antiinflammatory activity of some medicinal plant extracts from Venezuela Journal of Ethnopharmacology 55(1): 63-8.

Akinyemi, K.O., Bayagbon C., Oyefolu, A.O.B., Akinside K.A., Omonigbeyin E.A., Coker A.O. 2000. Antibacteria Sereening of five indigenous Nigerian medicinal plants against S. typhi and S. paratyph. Journal of Nigerian Infection Control Association 3 (1); 30-33.

Bailey, N.T. 1992. Statistical Methods in Biology, 2nd Ed., Cambridge University Press, Cambridgen 75-79.

Bradford, H.A., Hill, I.D. 1991. Principles of Medical Statistics, 12th Ed. Edward Arnold, London 14-23

Carlson, G. 1996. Clinical Chemistry Test. In. Smith B.P. ed. Large Animal Internal Medicine, 2nd ed. Baltimore, Bobsy, 463.

Diwan, P.V., Karwande, I.M., Sattur, P.B. 1989. Pharmacology and biochemical evaluation of Tridax procumbens on inflammation. Indian Journal of Pharm. 17 (3): 114-117.

Fakunle, J.O., Abatan, M.O. 2007. Toxicological effects of Tithonia diversifolia in rat. Journal of Animal and Veterinary Advances, Medwell Online 6 (10): 1223-1226.

Forestieri, A.M., Monforte M.T., Ragusa, S., Trovato, A. 1996. Antiinflammatory, analgesic and antipiretic activity in rodents of plants extracts used in African Medicine. Phytotherapy-Research, 10:2, 100 – 106.

Gornall, A.G., Bardawill, C.J., David, M.M. 1949. Determination of Serum protein by means of Biuret reagent. J. Biol. Chem. 177:751-755.

Guyton, A.C., Hall, J.E. 1994. Textbook of Medical Physiology. 9th Ed. W.B. Saunders Co., Philadelphia

Iwu, M., Igboko, O. 1982. Flavonoids of Garcinia kola seeds J. Nat. Prod. 45, 650-651.

Iwu, M. 1985. Antihepatotoxic constituents of Garcinia kola seed. Experimental, 41, 699-700.

Jain, N.C. 1986. Schalm’s Veterinary Haematology. 4th Ed. Lea and Fabiger, Philadelphia p 564-575.

Jendrassi, L., Goff, P. 1938. Vereinfaclite photometrische Methodenqur bestimming des blut bilirubins. Biochem. 297:81 – 84.

Kaneko, J.T., Cornelius, C.E. 1980. Clin. Bioch of Dom. Animals. News York, Academic Press.

Lee, K.H. 1968. Studies on the mechanism of action of salicylates II retardation of wound healing by aspirin. J. Pharm. Sci. 57 1042.

Meech, R.J. 1985. Proceedings of Immunology In Clinical Practice. Foundation for Continuing Education NZ Vet. Assoc. Pp. 140

Michealson, M. 1961. Bilirubin determination in serum and urine scand. J. Clin Lab. Invest. (Suppl. 56) 13:1.

Nosslin, B., 1960. The direct diazo reaction of bile pigments in serum scand J. Clin. Lab. Invest. (Suppl. 49) 12:1-4.

Schalm, O.W., Jain, N.C., Carroll, E.J. 1975. Veterinary Haematology 3rd Ed. Lea and Febiger, Philadelphia.

Sigma Diagnostics, 1985. Quantitative Colorimetric Determination in Serum, Plasma or Cerebrospinal Fluid (Procedure No. 505).
Section
Articles