Haematological and Biochemical Examination of Pulcherrimin A isolated from Caesalpinia pulcherrima stem bark doi.org/10.26538/tjnpr/v5i11.20

Main Article Content

Osahon K. Ogbeide
Isaac U. Akhigbe
Charles A. Unuigbe
Osayemwenre Erharuyi
Vincent Imieje
Gabriel O.Benjamin
Kingsley Ikeke
Bosede Ayeni
Emmanuel Irabor
Joseph B. Owolabi
Abiodun Falodun

Abstract

Caesalpinia pulcherrima has been utilised in the treatment of gastritis inflammation, diarrhoea dysentery, flatulence, ulcers, hepatitis, uterine dysfunction, rheumatism, haemorrhages and many other infections. The study evaluated the haematological and biochemical effects of pulcherrimin A isolated from C. pulcherrima stem bark. The compound, pulcherrimin A was administered to Wistar rats at doses of 2, 4 and 8 mg/kg body weight (bw) respectively for 28 days. The total blood count, total cholesterol, triglycerides, aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), gamma lutamyltranspeptidase  (GGT), total protein and total bilirubin were evaluated. The results showed a significant difference in white blood cell count at 2 mg/kg for female rats. Red blood cells and haemoglobin for both sexes appeared normal relative to control. The changes observed for platelets in all treated groups for both sexes were not significantly different from the control p˃0.05). The liver enzymes for the female rats appeared normal at all treatment doses, however, the glutamyltranspeptidase in male rats significantly increased at 2 mg/kg. The triglyceride and very low-density lipoproteins significantly decreased (p<0.05) for the female rats at 4 mg/kg. Findings from this study showed that pulcherrimin A have potential beneficial effects to reduce triglycerides and could facilitate the prevention of heart and liver related diseases.  

Downloads

Download data is not yet available.

Article Details

How to Cite
K. Ogbeide, O., U. Akhigbe, I., A. Unuigbe, C., Erharuyi, O., Imieje, V., O.Benjamin, G., Ikeke, K., Ayeni, B., Irabor, E., B. Owolabi, J., & Falodun, A. (2021). Haematological and Biochemical Examination of Pulcherrimin A isolated from Caesalpinia pulcherrima stem bark: doi.org/10.26538/tjnpr/v5i11.20. Tropical Journal of Natural Product Research (TJNPR), 5(11), 2011-2015. https://tjnpr.org/index.php/home/article/view/348
Section
Articles
Author Biography

Joseph B. Owolabi, Department of Chemistry, Faculty of Physical Sciences, University of Benin, Benin City, Nigeria

Department of Chemistry, School of Sciences, the Federal University of Technology, Akure, Nigeria

How to Cite

K. Ogbeide, O., U. Akhigbe, I., A. Unuigbe, C., Erharuyi, O., Imieje, V., O.Benjamin, G., Ikeke, K., Ayeni, B., Irabor, E., B. Owolabi, J., & Falodun, A. (2021). Haematological and Biochemical Examination of Pulcherrimin A isolated from Caesalpinia pulcherrima stem bark: doi.org/10.26538/tjnpr/v5i11.20. Tropical Journal of Natural Product Research (TJNPR), 5(11), 2011-2015. https://tjnpr.org/index.php/home/article/view/348

References

Dar RA, Shahnawaz M, Qazi PH. Natural product medicines: A literature update. J Phytopharmacol. 2017; 6(6):349-351.

Erharuyi O, Adhikari A, Falodun A, Imad R, Choudhary MI. Derivatization of cassane diterpenoids from Caesalpinia pulcherrima (L.) Sw. and evaluation of their cytotoxic and leishmanicidalactivities. Tetrahedron Lett. 2016; 57(20):2201-2206.

Ogbeide OK and Akhigbe IU. Anti-haemolytic, Antianaemic and Biosafety Examination of combined Telfairiaoccidentalis and Ipomoea batatas leaves extract. J Pharm Allied Sci. 2019; 16(4):3106-3113.

Ogbeide OK, Akhigbe IU, Unuigbe CA, Erharuyi O, Oseghale I, Imieje V, Iheanacho C, Ikeke K, Ayeni B, Irabor E, Owolabi JB, Falodun A. Isolation, characterization, and in vivo anti-malarial investigation of pulcherrimin A from Caesalpinia pulcherrima stem bark.GSC Biol Pharm Sci. 2020; 12(2):56-63.

World Health Organization (WHO). Traditional Medicine Fact sheet 2008; No. 134. [cited June 20th 2021]. Retrieved from: www.who.int/mediacentre/factsheets/fs134/en

Swanepoel C, Blockman M, Talmud J. Nephrotoxins in Africa. In: Clinical nephrotoxins: Renal injury from drugs and chemicals. Part 3. Metapress, Springer, New York. 2008. 859-870 p.

Mwale M, Masika PJ, Materechera SA. Effect of Medicinal Plants on Haematology and Serum Biochemical Parameters of Village Chickens Naturally Infected with Heterakis gallinarum. Bangl J Vet Med. 2014; 12(2):99-106.

Jaouad EIH, Zafar HI, Badiˆaa L. Acute and chronic toxicological studies of Ajugaiva in experimental animals. J Ethnopharmacol. 2004; 91(1):43-50.

Oduola T, Popoola GB, Avwioro OG, Oduola TA, Ademosun AA and Lawal MO. Use of Jatropha gossypifolia stem latex as a haemostatic agent: how safe is it? J Med Plants Res. 2007; 1(1):014-017.

West GD and Haines VL. Haematology and serum biochemistry values of captive Attwater's prairie chickens (Tympanuchus cupido). J Zoo Wildl Med. 2002; 33(2):122-124.

Schmidt EMS, Paulillo AC, Martins GRV, Lapera IM, Testi AJP, Junior LN, Denadai J and Fagliari JJ. Haematology of the bronze turkey (Meleagris gallopavo): Variations with age and gender. Int J Poul Sci. 2009; 8(8):752-754.

Kumbhare M and Sivakumar T. Anti-inflammatory and Antinociceptive activity of Pods of Caesalpinia pulcherrima. J Appl Pharm Sci. 2011; 1(7):180-184.

Pankaj N, Deepak N, Ranveer B. A Review on Phytochemical and Pharmalogical aspects of Caesalpinia pulcherrima. Int J Res. Ayurv Pharm. 2011; (2):416-421.

Ogbeide OK, Dickson VO, Jebba BJ, Owhiroro DA, Olaoluwa MO, Imieje VCO, Erharuyi, O, Owolabi BJ, Fasinu P, Falodun A. Anti-plasmodial and Acute Toxicity Studies of Fractions and Cassane-Type Diterpenoids from Stem Bark of Caesalpiniapulcherrima (L) Sw. Trop J Nat Prod Res. 2018;2(4):179-184.

NIH, Guide for the care and use of laboratory animals. U.S. Department of Health and Human Services, NIH Pub. 1985; 86:1-83.

Cornel C, Aurelia NC, Manuella M, Simona N, Zbarcea EC, Nuta DC. Pharmalogical Evaluation of Acute and Sub-acute Toxicity and Antidepressant effect after Acute Administration of Novel N-substituted Benzamides. Farmacia. 2010; 58(1):21-28.

Agbaje EO, Adeneye AA, Daramola AO. Biochemical and Toxicological Studies of Aqueous Extract of Syzigium aromaticum(L.) Merr. & Perry (Myrtaceae) in Rodents. Afr J Trad Compl Altern Med. 2009; 6(3):241–254.

Ibrahim MB, Sowemimo AA, Sofidiya MO, Badmos KB, Fageyinbo MS, Abdulkareem FB, Odukoya OA. Sub-acute and chronic toxicity profiles of MarkhamiatomentosaEthanolic leaf extract in rats. J Ethnopharmacol. 2016; 193 (2016):68-75.

Akuodor GC, Eban LK, Nku CO, Aja Daniel OJ, Ezeunala MN, Ajoku GA, Nwobodo N N. Haematological and biochemical changes after exposure to Maerunacrassifolia ethanol leaf extract in rats. J Appl Pharm Sci. 2017; 7(6):136-140.

Olso H, Betton G, Robinson D, Thomas K, Monro A, Kolaja G, Lilly P, Sanders J, Sipes G, Bracken W, Dorato M, Deun KV, Smith P, Berger B, Heller A. Concordance of the toxicity of pharmaceuticals in humans and in animals. RegulToxicolPharmacol. 2000; 32(1):6–67.

Balakrishna S and Prabhune AA. Gammaglutamyltransferases: A structural, mechanistic and physiological perspective. Front Biol. 2014; 9:51-65.

Rader DJ and Hovingh GK. Lipids and cardiovascular disease 2: HDL and cardiovascular disease. Lancet. 2014; 384:618-625.

Ahn N and Kim K. High-density lipoprotein cholesterol (HDL-C) in cardiovascular disease: effect of exercise training. Integr Med Res. 2016; 5(3)212-215.24. He Y, Kothari V, Bornfeldt KE. High-Density Lipoprotein Function in Cardiovascular Disease and Diabetes Mellitus.

ArteriosclerThrombVasc Biol. 2018; 38(2):e10-e16.