Generic placeholder image

Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry

Editor-in-Chief

ISSN (Print): 1871-5230
ISSN (Online): 1875-614X

Research Article

Effects of Kolaviron on Pneumonia-like Infection Induced in Albino Wistar Rats

Author(s): Ogechukwu Calista Dozie-Nwakile, Nwakile Calistus Dozie, Uchendu Ikenna Kingsley*, Okonkwo Francis Catherine and Onyemelukwe Ngozi Felicia

Volume 20, Issue 2, 2021

Published on: 15 September, 2020

Page: [219 - 227] Pages: 9

DOI: 10.2174/1871523019666200915085729

Price: $65

Open Access Journals Promotions 2
Abstract

Background: Pneumonia is an acute or chronic inflammatory disorder of the lungs, affecting the mucosal areas of the lung. It can be caused by bacteria, viruses or fungi. In some cases, it may be caused by physical or chemical irritants. Kolaviron, a natural bioflavonoid extract from Garcinia kola seeds, has been shown to possess anti-inflammatory properties in Flu-like conditions which are associated with cough. There has been a paucity of information on the likelihood of the effectiveness of kolaviron against pneumonia infections.

Objective: To evaluate the antibacterial and anti-inflammatory effects of kolaviron on albino Wistar rats induced with pneumonia using Klebsiella pneumonia.

Materials and Methods: Powdered Garcinia kola seeds were extracted with n-hexane and 100% methanol as solvents by using Soxhlet extractor. A standard method was used to obtain kolaviron from the seed extracts. A total of 24 albino Wistar rats were randomly divided into six groups A to F, each comprising four rats. The rats were allowed to acclimatize for 1 hour in very cold environments using ice packs. A standardized 1.0 x10 -5 mg/ml culture suspension was intranasally inoculated to the rats for 10 days to induce pneumonia-like symptoms. Thereafter, the kolaviron was administered to the rats such that a 500mg/kg kolaviron extract was given once daily to groups A (male rats) and B (female rats). Groups C (male rats) and D (female rats) received 250mg/kg of kolaviron extract once daily, while group E rats were given 0.5 ml of dimethyl sulfoxide (DMSO) once daily, which served as the negative control. The rats in Group F received 2.86 mg/kg of ofloxacin once daily and served as the positive control. All the treatments were done for a period of 5 days. Then 10 days after the treatments, the animals were sacrificed and the lungs were harvested for hydrostatic lung test and histopathological examination. An overnight broth culture of Klebsiella pneumonia was streaked in sterile molten nutrient agar maintained at 37°C for 24hrs. Later, a stock of 500mg/ml of kolaviron was prepared in DMSO. Two-fold dilutions were performed to obtain the following concentrations of 100%, 50%, 25%, 12.5%, 6.25%, 3.125%, and 1.565% with the stock. The anti-Klebsiella pneumonia activity of the kolaviron extract was determined using agar well diffusion methods and incubation was done at 37 o C for 24 hrs. Student t-test and Oneway Analysis of variance (ANOVA) were used for comparison of mean differences between and among the groups.

Results and Discussion: The sensitivity of Klebsiella pneumonia to kolaviron was concentration- dependent. There was an increase in anti-Klebsiella pneumonia activity with a decrease in kolaviron concentration. Kolaviron (KV), at 500mg/kg concentration, was efficacious and showed significant anti-inflammatory effects (P<0.0001). This was also confirmed in the histopathological examinations. The 3.125% concentration of the kolaviron gave IZDs that ranged from 25.68±3.33 mm on day 1 to 27.33±2.78 mm on day 5. Treatment with kolaviron showed to be sex-dependent with a significant difference (p<0.0001), when pre-treatment and post-treatment effects were compared between male and female rats.

Conclusion: Kolaviron can be used as an agent in the treatment of pneumonia as it possesses anti- inflammatory and anti-Klebsiella pneumonia activities.

Keywords: Bitter kola, garcinia kola extracts, kolaviron, klebsiella pneumonia, pneumonia-like symptoms in rat, anti-inflammatory.

« Previous
Graphical Abstract
[1]
Elujoba, A.A.; Odeleye, O.M.; Ogunyemi, C.M. Traditional medical development for medical and dental primary health care delivery system in Africa. Afr. J. Tradit. Complem., 2005, 2(1), 46-61.
[2]
Okigbo, R.N.; Mmeka, E.C. Antimicrobial effects of three tropical plant extracts on Staphylococcus aureus, Escherichia coli and Candida albicans. Afr. J. Tradit. Complement. Altern. Med., 2008, 5(3), 226-229.
[http://dx.doi.org/10.4314/ajtcam.v5i3.31277] [PMID: 20161941]
[3]
Uchendu, I.K.; Okoroiwu, H.U. Evaluation of blood oxidant/antioxidant changes and testicular toxicity after subacute exposure to cadmium in albino rats: Therapeutic effect of Nigella sativa seed extracts. Comb. Chem. High Throughput Screen., 2020, 23, 1.
[http://dx.doi.org/10.2174/1386207323666200526134923] [PMID: 32452325]
[4]
Uchendu, I.K.; Okoroiwu, H.U. Nigella sativa seed protects against cadmium-induced renal toxicity in rats. Curr. Chem. Biol., 2020, 14, 1.
[http://dx.doi.org/10.2174/2212796814666200520083818]
[5]
Ajibesin, K.K. Dacryodes edulis (G. Don) HJ. Lam: A review on its medicinal, phytochemical and economic properties. Res. J. Med. Plant, 2011, 5(1), 32-41.
[http://dx.doi.org/10.3923/rjmp.2011.32.41]
[6]
Okigbo, R.N.; Ajalie, A.N. Inhibition of some human pathogens with tropical plant extracts. IJMMAS, 2005, 1(1), 34-41.
[7]
Cocanour, C.S.; Chang, P.; Huston, J.M.; Adams, C.A., Jr; Diaz, J.J.; Wessel, C.B.; Falcione, B.A.; Bauza, G.M.; Forsythe, R.A.; Rosengart, M.R. Management and novel adjuncts of necrotizing soft tissue infections. Surg. Infect. (Larchmt.), 2017, 18(3), 250-272.
[http://dx.doi.org/10.1089/sur.2016.200] [PMID: 28375805]
[8]
Alverdy, J.C.; Krezalek, M.A. Collapse of the microbiome, emergence of the pathobiome and the immunopathology of sepsis. Crit. Care Med., 2017, 45(2), 337-347.
[http://dx.doi.org/10.1097/CCM.0000000000002172] [PMID: 28098630]
[9]
Masters, I.B.; Isles, A.F.; Grimwood, K. Necrotizing pneumonia: an emerging problem in children? Pneumonia (Nathan), 2017, 9(1), 11.
[http://dx.doi.org/10.1186/s41479-017-0035-0] [PMID: 28770121]
[10]
Farombi, E.O.; Shrotriya, S.; Surh, Y.J. Kolaviron inhibits dimethyl nitrosamine-induced liver injury by suppressing COX-2 and iNOS expression via NF-kappaB and AP-1. Life Sci., 2009, 84(5-6), 149-155.
[http://dx.doi.org/10.1016/j.lfs.2008.11.012] [PMID: 19081081]
[11]
Olaleye, S.B.; Farombi, E.O.; Adewoye, E.A.; Owoyele, B.V.; Onasanwo, S.A.; Elegbe, R.A. Analgesic and anti-inflammatory effects of kolaviron (a Garcinia kola seed extract). Afr. J. Biomed. Res., 2000, 3, 171-174.
[12]
Uko, O.J.; Usman, A.; Ataja, A.M. Some biological activities of Garcinia kola in growing rats. Vet. Arh., 2001, 71, 287-297.
[13]
Adesuyi, A.O.; Elummi, I.K.; Adatamola, F.B.; Nwokocha, A.G.M. Nutritional and Phytochemical screening of Garcinia kola. Adv. J. Food Sci. Technol., 2012, 4(1), 9-14.
[14]
Iwu, M.W.; Duncan, A.R.; Okunji, C.O. New antimicrobials of plant origin.Janick J (ed.), Perspectives on new crops and new uses; ASHS Press, Alexandria, VA., 1999, pp. 457-462.
[15]
Oyagbemi, A.A.; Omobowale, T.O.; Adedapo, A.A.; Yakubu, M.A. Kolaviron, biflavonoid complex from the seed of Garcinia kola attenuated angiotensin II-and lypopolysaccharide-induced vascular smooth muscle cell proliferation and nitric oxide production. Pharmacognosy Res., 2016, 8(Suppl. 1), S50-S55.
[http://dx.doi.org/10.4103/0974-8490.178647] [PMID: 27114693]
[16]
Tamuno-Emine, D.G.; Anyia, A.F. Protective effect of Garciniakola seed and honey mixture against cadmium-induced hepatotoxicity in wistar albino rats. IJSR, 2016, 5(5), 356-363.
[http://dx.doi.org/10.21275/v5i5.NOV163054]
[17]
Akintonwa, A.; Essien, A.R. Protective effects of Garcinia kola seed extract against paracetamol-induced hepatotoxicity in rats. J. Ethnopharmacol., 1990, 29(2), 207-211.
[http://dx.doi.org/10.1016/0378-8741(90)90057-Z] [PMID: 2374432]
[18]
Farombi, E.O. Mechanisms for the hepatoprotective action of kolaviron: studies on hepatic enzymes, microsomal lipids and lipid peroxidation in carbontetrachloride-treated rats. Pharmacol. Res., 2000, 42(1), 75-80.
[http://dx.doi.org/10.1006/phrs.1999.0648] [PMID: 10860638]
[19]
Rosenberg, L.N.; Peppercorn, M.A. Efficacy and safety of drugs for ulcerative colitis. Expert Opin. Drug Saf., 2010, 9(4), 573-592.
[http://dx.doi.org/10.1517/14740331003639412] [PMID: 20377475]
[20]
Iwu, M. Igboko, O. Flavonoids of Garcinia kola seeds. J. Nat. Prod., 1982, 45(5), 650-650.
[http://dx.doi.org/10.1021/np50023a026]
[21]
Farombi, E.O.; Adedara, I.A.; Ajayi, B.O.; Ayepola, O.R.; Egbeme, E.E. Kolaviron, a natural antioxidant and anti-inflammatory phytochemical prevents dextran sulphate sodium-induced colitis in rats. Basic Clin. Pharmacol. Toxicol., 2013, 113(1), 49-55.
[http://dx.doi.org/10.1111/bcpt.12050] [PMID: 23336970]
[22]
Adegoke, A.A.; Adebayo-Tayo, B.C. Antibacterial activity and phytochemical analysis of leaf extracts of Lasienthera africanum. Afr. J. Biotechnol., 2009, 8(1), 71-80.
[23]
Herías, M.V.; Koninkx, J.F.; Vos, J.G.; Huis in’t Veld, J.H.; van Dijk, J.E. Probiotic effects of Lactobacillus casei on DSS-induced ulcerative colitis in mice. Int. J. Food Microbiol., 2005, 103(2), 143-155.
[http://dx.doi.org/10.1016/j.ijfoodmicro.2004.11.032] [PMID: 16083817]
[24]
Seril, D.N.; Liao, J.; Yang, G.Y.; Yang, C.S. Oxidative stress and ulcerative colitis-associated carcinogenesis: studies in humans and animal models. Carcinogenesis, 2003, 24(3), 353-362.
[http://dx.doi.org/10.1093/carcin/24.3.353] [PMID: 12663492]
[25]
Mouzaoui, S.; Rahim, I.; Djerdjouri, B. Aminoguanidine and curcumin attenuated tumor necrosis factor (TNF)-α-induced oxidative stress, colitis and hepatotoxicity in mice. Int. Immunopharmacol., 2012, 12(1), 302-311.
[http://dx.doi.org/10.1016/j.intimp.2011.10.010] [PMID: 22036766]
[26]
Adegboye, M.F.; Akinpelu, D.A.; Okoli, A.I. The bioactive and phytochemical properties of G. kola (Heckel) seed extract on some pathogens. Afr. J. Biotechnol., 2008, 7(21), 3938-3938.
[27]
Akinnibosun, F.I.; Itedjere, E. Evaluation of the antibacterial properties and synergistic effect of Garcicnia kola Heckel (Family: Guttiferae) seed extract and honey on some bacteria. Afr. J. Microbiol. Res., 2013, 7(3), 174-180.
[28]
Ayepola, O.R.; Brooks, N.L.; Oguntibeju, O.O. Kolaviron improved resistance to oxidative stress and inflammation in the blood (erythrocyte, serum, and plasma) of streptozotocin-induced diabetic rats. Sci. World J., 2014, 2014, 921080.
[http://dx.doi.org/10.1155/2014/921080] [PMID: 24795542]
[29]
Bukar, B.B.; Uguru, M.O.; Omolola, A.; Wannang, N.N. Phytochemical analysis and effects of chronic and sub-chronic administrations of methanolic seed extract of garcinia kola (heckel) on some physiological parameters in male rodents: relevance on traditional claim of its aphrodisiac properties. Int. J. Phytopharm., 2016, 7(3), 100-107.
[30]
Mazi, E.A.; Okoronkwo, K.A.; Ibe, U.K. Physico-chemical and nutritive properties of bitter kola (Garcinia kola). Nutr. Food Sci., 2013, 3, 4.
[http://dx.doi.org/10.4172/2155-9600.1000218]
[31]
Awogbindin, I.O.; Olaleye, D.O.; Farombi, E.O. Kolaviron improves morbidity and suppresses mortality by mitigating oxido-inflammation in BALB/c mice infected with influenza virus. Viral Immunol., 2015, 28(7), 367-377.
[http://dx.doi.org/10.1089/vim.2015.0013] [PMID: 26200137]
[32]
Gamache, J.; Harrington, A. Bacterial Pneumonia Pulmonology, 2000.https://emedicine.medscape.com/article/300157-overview#a5

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy