Startseite Curative effects of Distemonanthus benthamianus Baillon. Trunk-bark extracts on enteropathogenic Escherichia coli 31-induced diarrhea in rats
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Curative effects of Distemonanthus benthamianus Baillon. Trunk-bark extracts on enteropathogenic Escherichia coli 31-induced diarrhea in rats

  • Yousseu Nana William , Ateufack Gilbert EMAIL logo , Abdul Jabbar Shah , Fazli Wahid , Mbiantcha Marius , Muhammad Arfat Yameen , Syed Luqman Shah , Kashif Bashir , Wasim Sajjad , Jules-Roger Kuiate , Kamanyi Albert und Taous Khan EMAIL logo
Veröffentlicht/Copyright: 23. Mai 2019

Abstract

Background

Distemonanthus benthamianus is used in the Western part of Cameroon to treat diarrheal episodes and infections. This study assessed its trunk-bark extracts activity against enteropathogenic Escherichia coli 31 (EPEC 31)-induced diarrhea in rats.

Methods

Aqueous and methanolic extracts were analyzed through high-performance liquid chromatography (HPLC). In vitro minimum inhibitory and bactericidal concentrations (MICs/MBCs) were evaluated on Enterococcus faecalis (ATCC 10,541), E. coli (ATCC 6539), Klebsiella pneumoniae (ATCC 13,883), Salmonella typhi (ATCC 6539) strains and on Proteus mirabilis, Pseudomonas aeruginosa (PA 01) and Shigella flexneri isolates using the microdilution method. Diarrhea was induced by inoculating rats with EPEC 31 (1.5 × 108CFU/mL; p.o). Serum transaminases level assay and enzyme-linked immunosorbent assay (ELISA) for cytokines determination were performed. Hematoxylin–eosin (H–E) staining was used for intestinal tissue analysis.

Results

HPLC fingerprints of extracts showed presence of gallic acid and other unidentified compounds. The lowest MIC of 256 µg/mL was obtained with methanolic extract. At 100 mg/kg, both extracts significantly (p<0.001) inhibited diarrhea, with the methanolic extract being the most active. In addition, the methanolic extract significantly (p<0.001) increased the relative mass of the liver compared to negative control (Tween-DMSO 8%). The aqueous extract (100 mg/kg) significantly (p<0.01) increased alanine aminotransferase (ALT) serum concentration; while the methanolic extract (100 mg/kg) exhibited similar effect over aspartate aminotransferase (AST). At 50 and 100 mg/kg, the methanolic extract significantly (p<0.05 and p<0.01) decreased the Interleukin-1β (IL-1β) serum level, compared to negative control (Tween-DMSO 8%). Serum level of tumor necrosis factor alpha (TNF-α) significantly (p<0.001) decreased with 100 mg/kg of aqueous extract and all doses of methanolic extract. Inhibition of inflammatory cells tissue infiltration and epithelial regeneration was highly noticed in the ileum and colon of extracts-treated rats than in ciprofloxacin-treated animals.

Conclusion

These findings suggest that D. benthamianus trunk-bark extracts displayed therapeutic effects against infectious diarrhea in rats.

Acknowledgments

The authors would like to express their thanks to the CIIT-TWAS Sandwich Postgraduate Fellowship [FR number: 3240293217, 2016], awarded to YNW for financial support.

  1. Author contributions: YNW collected plant material, performed laboratory work, statistical analysis and prepared the manuscript. AG, AJS, KA and TK conceived the idea, revised the manuscript and supervised the study. FW and MM provided punctual assistances and contributed in raw data analysis. MAY provided the bacterial isolate (EPEC 31) and laboratory facilities. SLS and WS helped in animals feeding and laboratory work. KB helped performing the HPLC fingerprint assay. J-RK provided bacterial strains and laboratory facilities for anti-enterobacterial tests. All authors critically read and approved the final manuscript for submission.

  2. Research funding: CIIT-TWAS Sandwich Postgraduate Fellowship [FR number: 3,240,293,217, 2016].

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

[1] Carlos CC, Saniel MC. Etiology and epidemiology of diarrhoea. Phillipine J Microbiol Infect Dis 1990;19:51–3.Suche in Google Scholar

[2] Paul K. Infectious diarrhoea. Med.2015;43:253–8.10.1016/j.mpmed.2015.02.005Suche in Google Scholar

[3] Foster MA, Iqbal J, Zhang C, Mc Henry R, Cleveland BE, Romero-Herazo Y, et al. Enteropathogenic and enteroaggregative E. coli in stools of children with acute gastroenteritis in Davidson County, Tennesse. Diagn Microbiol Infect Dis 2015;83:319–24.10.1016/j.diagmicrobio.2015.07.016Suche in Google Scholar PubMed PubMed Central

[4] Lai Y, Rosenshine I, Leong JM, Frankel G. Intimate host attachment: enteropathogenic and enterohaemorrhagic Escherichia coli. Cell Microbiol 2013;15:1796–808.10.1111/cmi.12179Suche in Google Scholar PubMed PubMed Central

[5] Roman C, Solh T, Broadhurst M. Infectious Diarrhoea. Phys Assist Clin 2017;2:229–45.10.1016/j.cpha.2016.12.006Suche in Google Scholar

[6] UNICEF/WHO. Diarrhoea: Why children are still dying and what can be done. The United Nations Children’s Fund (UNICEF)/World Health Organization (WHO). 2009:1–44.Suche in Google Scholar

[7] Sun Y, Kim SW. Intestinal challenge with enterotoxicogenic Escherichia coli in pigs and nutritional intervention to prevent postweaning diarrhoea. Anim Nutri 2017;3:322–30.10.1016/j.aninu.2017.10.001Suche in Google Scholar PubMed PubMed Central

[8] Jamwal K, Bhattacharya S, Puri S. Plant growth regulator mediated consequences of secondary metabolites in medicinal plants. J Appl Res Med Arom Plants 2018;9:26–38.10.1016/j.jarmap.2017.12.003Suche in Google Scholar

[9] Verhelst R, Shroyen M, Buys N, Niewold TA. E. coli heat labile toxin (LT) inactivation by specific polyphenols is aggregation dependent. Vet Microbiol 2013;163:319–24.10.1016/j.vetmic.2012.12.039Suche in Google Scholar PubMed

[10] Kareem KT, Oluwatoyin AS, Olabibi AA, Rashidat EA, Oluwatoyin AT. Antibacterial effect of Distemonanthus benthamianus extract against some oral pathogens. Intern J Appl Sci Technol 2012;2:114–9.Suche in Google Scholar

[11] Nguelefack EM, Kathleen BN, Alex A, Théophile D, Nole T, Joseph, et al. Phytochemical composition and in vitro effects of the ethyl acetate bark extract of Distemonanthus benthamianus Baillon (Caesalpiniaceae) on Staphylococcus aureus and Streptococcus agalactiae. Cameroon J Experiment Biol 2005;1:50–3.10.4314/cajeb.v1i1.37927Suche in Google Scholar

[12] Mebude OO, Adeniyi BA, Lawal O. In vitro antimicrobial activities of ethanol extract of Distemonanthus benthamianus (Aayan) Baillon (Fabaceae) on Streptococcus mutans. British J Med Medic Res 2017;22:1–8.10.9734/BJMMR/2017/26954Suche in Google Scholar

[13] Saha J-BT, Pétrissans A, Molina S, Ndikontar MK, Mounguengui S, Dumarçay S, et al. Study of the feasibility of a natural dye on cellulosic textile supports by red padouk (Pterocarpus soyauxii) and yellow movingui (Distemonanthus benthamianus) extracts. Indust Crops Prod 2014;60:291–7.10.1016/j.indcrop.2014.06.029Suche in Google Scholar

[14] King FE, King TJ, Stokes PJ. The chemistry of extractives from hardwoods. Part XIX. The structures of further new flavones occurring in ayan (Distemonanthus benthamianus). J Chem Society 1954a;4587–94.10.1039/jr9540004587Suche in Google Scholar

[15] King FE, King TJ, Stokes PJ. The chemistry of extractives from hardwoods. Part XX. Distemonanthin, a new type of flavone pigment from Distemonanthus benthamianus. J Chem Society 1954b;4594–600.10.1039/jr9540004594Suche in Google Scholar

[16] Malan E, Naidoo S. Two flavanols from Distemonanthus benthamianus. Phytochemistry 1980;19:2731–3.10.1016/S0031-9422(00)83952-7Suche in Google Scholar

[17] Malan E, Naidoo S. A hexa-substituted flavonol from Distemonanthus benthamianus. Phytochemistry 1990;29:2366.10.1016/0031-9422(90)83079-GSuche in Google Scholar

[18] Malan E. A flavonol with a tetrasubstituted B-ring from Distemonanthus benthamianus. Phytochemistry 1993;32:1631–2.10.1016/0031-9422(93)85198-ZSuche in Google Scholar

[19] Malan E, Swinny E, Ferreira D. A 3-oxygenated flavolignoid from Distemonanthus benthamianus. Phytochemistry 1994;37:1771–2.10.1016/S0031-9422(00)89611-9Suche in Google Scholar

[20] Salako OA, Akindele AJ, Omotoyosi MS, Elegunde OO. Antidiarrhoeal activity of aqueous leaf extract of Caladium bicolor (Araceae) and its possible mechanisms of action. J Ethnopharmacol 2015;176:225–31.10.1016/j.jep.2015.10.035Suche in Google Scholar PubMed

[21] Newton SM, Lau C, Gurcha SS, Besra GS, Wright CW. The evaluation of forty-three plant species for in vitro antimycobacterial activities; isolation of active constituents from Psoralea corylifolia and Sanguinaria canadensis. J Ethnopharmacol 2002;79:57–67.10.1016/S0378-8741(01)00350-6Suche in Google Scholar PubMed

[22] Ateufack G, Tadjoua TH, Yousseu WN, Sama FL, Kuiate J-R, Kamanyi A. Antidiarrhoeal and antibacterial activity of aqueous and methanolic leaves extracts of Dissotis thollonii Cogn. (Melastomataceae). Asian Pac J Trop Biomed 2014;4:S672–78.10.12980/APJTB.4.201414B214Suche in Google Scholar

[23] Shirpoor A, Barmaki H, Ansari MK, Ikhanizadeh B, Barmaki H. Protective effect of vitamine E against ethanol-induced small intestine damage in rats. Biomed Pharmacother 2016;78:150–5.10.1016/j.biopha.2016.01.015Suche in Google Scholar PubMed

[24] Christian N What is diarrhoea? What causes diarrhoea? The MNT KNOWLEDGE center. Gastrointestinal/Gastroenterology. Available at: https://www.medicalnewstoday.com/categories/gastrointestinal. Assessed: 15 Apr 2014.Suche in Google Scholar

[25] Mašković PZ, Veličković V, Durović Zeković Z, Radojković M, Cvetonović A, Švarc-Gajić J, et al. Biological activity and chemical profile of Lavatera thuringiaca L. extracts obtained by different extraction approaches. Phytomed 2018;38:118–24.10.1016/j.phymed.2017.11.010Suche in Google Scholar PubMed

[26] Carvalho RS, Carollo CA, de Magalhães JC, Palumbo JM, Boaretto AG, Nunes E Sá IC, et al. Antibacterial and antifungal activities of phenolic compound-enriched ethyl acetate fraction from Cochlospermum regium (mart. Et. Schr.) Pilger roots: mechanisms of action and synergism with tannin and gallic acid. South African J Bot 2018;114:181–7.10.1016/j.sajb.2017.11.010Suche in Google Scholar

[27] Chen Y-W, Ye S-R, Ting C, Yu Y-H. Antibacterial activity of propolins from Taiwanese green propolis. J Food and Drug Anal 2018;26:761–8.10.1016/j.jfda.2017.10.002Suche in Google Scholar PubMed

[28] Ngankeu PA, Tamokou JD, Lateef M, Tapondjou LA, Kuiate J-R, Ngnokam D, et al. New triterpene and new flavones glucoside from Rhynchospora corymbosa (Cyperaceae) with their antimicrobial, tyrosinase and butyrylcholinesterase inhibitory activities. Phytochem Lett 2016;16:121–8.10.1016/j.phytol.2016.03.011Suche in Google Scholar

[29] Eric S. Doxycycline. Encyclopedia xpharm. Comprehens. Pharmacol. Ref. Elsevier Inc. 2007;1–8.10.1016/B978-008055232-3.61651-4Suche in Google Scholar

[30] Novacco M, Sugiarto S, Willi B, Baumann J, Spiri AM, Oestmann A, et al. Consecutive antibiotic treatment with doxycycline and marbofloxacin clears bacteremia in Mycoplasma haemofelis-infected cats. Veterin Microbiol 2018;217:112–20.10.1016/j.vetmic.2018.03.006Suche in Google Scholar PubMed

[31] Zhang D, Zhang K, Su W, Zhao Y, Ma X, Qian G, et al. Aquaporin-3 is down-regulated in jejunum villi epithelial cells during enterotoxicogenic Escherichia coli-induced diarrhoea in mice. Microb Pathogen 2017;107:430–5.10.1016/j.micpath.2017.04.031Suche in Google Scholar PubMed

[32] Yong A-L, Ooh K-F, Ong H-C, Chai -T-T, Wong F-C. Investigation of antibacterial mechanism and identification of bacterial protein targets mediated by antibacterial medicinal plant extracts. Food Chem 2015;186:32–6.10.1016/j.foodchem.2014.11.103Suche in Google Scholar PubMed

[33] Kurtz JR, Goggins AJ, Mc Lachlan JB. Salmonella infection: interplay between the bacteria and host immune system. Immunol Lett 2017;190:42–50.10.1016/j.imlet.2017.07.006Suche in Google Scholar PubMed PubMed Central

[34] Lawan A, Jesse FF, Idris UH, Odhah MN, Arsalan M, Muhammad NA, et al. Mucosal and systemic responses of immunogenic vaccines candidates against enteric Escherichia coli infections in ruminants. A rev Microb Pathogen 2018;117:175–83.10.1016/j.micpath.2018.02.039Suche in Google Scholar PubMed

[35] Genís S, Sánchez-Chardi A, Bach A, Fàbregas F, Arís A. A combination of lactic acid bacteria regulates Escherichia coli infection and inflammation of the bovine endometrium. J Dairy Sci 2017;100:1–14.10.3168/jds.2016-11671Suche in Google Scholar PubMed

[36] Noack M, Kolopp-Sarda M-N. Cytokines and inflammation: physiology, pathophysiology and therapeutic usage. Lab French Rev 2018;499:28–37.10.1016/S1773-035X(18)30052-2Suche in Google Scholar

[37] Peñaloza HF, Schultz BM, Nieto PA, Salazar GA, Suazo I, Gonzalez PA, et al. Opposing roles of IL-10 in acute bacterial infection. Cytokine Growth Fact Rev 2016;32:17–30.10.1016/j.cytogfr.2016.07.003Suche in Google Scholar PubMed

[38] Kumar A, Agarwal K, Singh M, Saxena A, Yadav P, Maurya AK, et al. Essential oil from waste leaves of Curcuma longa L. alleviates skin inflammation. Inflammopharmacology 2018;26:1245–55.10.1007/s10787-018-0447-3Suche in Google Scholar PubMed

[39] Ricciuto A, Kamath BM, Walters TD, Frost K, Carman N, Church PC, et al. New onset auto-immune hepatitis during anti-tumor necrosis factor alpha treatment in children. J Pediatr 2018;194:128–35.10.1016/j.jpeds.2017.10.071Suche in Google Scholar PubMed

[40] da S Pereira A, Souza de OL, Faccin LT, Baldissarelli J, Palma TV, Pereira Soares MS, et al. Effect of gallic acid on purigenic signaling in lymphocytes, platelets, and serum of diabetic rats. Biomed Pharmacother 2018;101:30–6.10.1016/j.biopha.2018.02.029Suche in Google Scholar PubMed

[41] Song L, Tian L, Ma Y, Xie Y, Feng H, Qing F, et al. Protection of flavonoids from Smilax china L. rhizome on phenol mucilage-induced pelvic inflammation in rats by attenuating inflammation and fibrosis. J Funct Foods 2017;28:194–204.10.1016/j.jff.2016.11.015Suche in Google Scholar

[42] Rehman MU, Zhang H, Wang Y, Mehmood K, Huang S, Iqbal MK, et al. Experimental mouse lethality of Escherichia coli strains isolated from free ranging Tibetan yaks. Microb Pathogen 2017;109:15–19.10.1016/j.micpath.2017.05.020Suche in Google Scholar PubMed

[43] Tan S, Barker N. Epithelial stem cells and intestinal cancer. Semin Cancer Biol 2015;32:40–53.10.1016/j.semcancer.2014.02.005Suche in Google Scholar PubMed

[44] Okamoto R. Epithelial regeneration in inflammatory bowel diseases. Inflamm Regener 2011;31:275–81.10.2492/inflammregen.31.275Suche in Google Scholar

[45] Abarca-Buis RF, Martínez-Jiménez A, Vera-Gómez E, Contreras-Figueroa ME, Garciadiego-Cázares D, Paus R, et al. Mechanisms of epithelial thickening due to IL-1 signaling blockade and TNF-α administration differ during wound repair and regeneration. Differentiation 2018;99:10–20.10.1016/j.diff.2017.12.001Suche in Google Scholar PubMed

[46] De Santana Souza MT, Teixeira DF, de Oliveira JP, Oliveira AS, Quintans-Júnior LJ, Correa CB, et al. Protective effect of carvacrol on acetic acid-induced colitis. Biomed Pharmacother 2017;96:313–9.10.1016/j.biopha.2017.10.017Suche in Google Scholar PubMed

[47] Mounanga MB, Mewono L, Angone SA. Toxicity studies of medicinal plants used in sub-saharan Africa. J Ethnopharmacol 2015;174:618–27.10.1016/j.jep.2015.06.005Suche in Google Scholar PubMed

[48] Singh A, Bhat TK, Sharma OP. Clinical Biochemistry of Hepatotoxicity. J Clin Toxicol 2011;4:1–19.Suche in Google Scholar

[49] Aouachria S, Boumerfeg S, Benslama A, Benbacha F, Guemmez T, Khennouf S, et al. Acute, sub-acute toxicity and antioxidant activities (in vitro and in vivo) of Reichardia picroide crude extract. J Ethnopharmacol 2017;208:105–16.10.1016/j.jep.2017.06.028Suche in Google Scholar PubMed

[50] Bagues NC, de Pinheiro Cristiane GM, Bastos LA, Fraga DB, Veras PS, Pontes-de-Carvalho LC, et al. Parasitic load and histological aspects in different regions of the spleen of dogs with visceral leishmaniasis. Comparative Imm Microbiol Infect Dis 2018;56:14–9.10.1016/j.cimid.2017.11.003Suche in Google Scholar PubMed

Received: 2018-10-27
Accepted: 2019-01-31
Published Online: 2019-05-23

© 2019 Walter de Gruyter GmbH, Berlin/Boston

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