Crude extracts from Diospyros gilletii stem bark attenuate Shigella flexneri-induced diarrhea in mice

Bijou-Lafortune Noumboue Kouamou , Boniface Pone Kamdem , Vincent Ngouana , Tashie Evangeline Ngwanguong , Jaurès Marius Tsakem Nangap , Listone Monelle Nzeye Ngameni , Yanick Kevin Dongmo Melogmo , Paul Keilah Lunga , Fabrice Fekam Boyom

Asian Pacific Journal of Tropical Biomedicine ›› 2025, Vol. 15 ›› Issue (6) : 219 -228.

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Asian Pacific Journal of Tropical Biomedicine ›› 2025, Vol. 15 ›› Issue (6) : 219 -228. DOI: 10.4103/apjtb.apjtb_713_24
Original Article

Crude extracts from Diospyros gilletii stem bark attenuate Shigella flexneri-induced diarrhea in mice

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Abstract

Objective: To evaluate the anti-shigellosis activity of the hydroethanol extract of Diospyros gilletii (D. gilletii) stem bark in Shigella flexneri (S. flexneri)-induced diarrheal mice.

Methods: The hydroethanolic extract was obtained by maceration of D. gilletii stem bark in 70% hydroethanol (waterethanol; 30:70, v/v) solution. Then, mice pretreated with cyclophosphamide for immunosuppression were administered orally with an inoculum containing S. flexneri, and subsequently treated with 100, 200, and 400 mg/kg of the hydroethanol extracts for 10 days. The bacterial colonies were enumerated and hematological and biochemical parameters were determined. Serum pro-inflammatory mediators including IL-1β, IL-18, and TNF-α, and nitric oxide levels were quantified by ELISA. Histological analyses of the kidney, liver, and colon were also conducted.

Results: Treatment with 200 and 400 mg/kg of the hydroethanolic extracts markedly inhibited the growth of S. flexneri. Moreover, treatment with D. gilletii extract downregulated the levels of IL-1β, IL-18, and TNF-α, and restored hematological and biochemical parameters as well as histological architecture of the colon, liver, and kidneys. Additionally, the oral administration of 2000 mg/kg D. gilletii extract did not induce any sign of toxicity, with a median lethal dose greater than 2000 mg/kg.

Conclusions: D. gilletii extract demonstrates the anti-shigellosis effects in S. flexneri-induced diarrheal mice, supporting the traditional use of this plant in treating diarrhea.

Keywords

Diospyros gilletti / Shigella flexneri / Diarrhea / Pro-inflammatory cytokines / Acute toxicity / Shigellosis

Cite this article

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Bijou-Lafortune Noumboue Kouamou, Boniface Pone Kamdem, Vincent Ngouana, Tashie Evangeline Ngwanguong, Jaurès Marius Tsakem Nangap, Listone Monelle Nzeye Ngameni, Yanick Kevin Dongmo Melogmo, Paul Keilah Lunga, Fabrice Fekam Boyom. Crude extracts from Diospyros gilletii stem bark attenuate Shigella flexneri-induced diarrhea in mice. Asian Pacific Journal of Tropical Biomedicine, 2025, 15(6): 219-228 DOI:10.4103/apjtb.apjtb_713_24

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Acknowledgments

The authors acknowledge the Biodefense and Emerging Infections Research Resources Repository (BEI Resources, Rockville, United States of America) for donating the reference strain Shigella flexneri NR 518.

Funding

This research was funded by the Yaounde-Bielefeld Bilateral Graduate School for Natural Products with Anti-parasite and Antibacterial Activity (YaBiNaPA) (grant number: 57316173).

Data availability statement

The data supporting the findings of this study are available from the corresponding authors upon request.

Authors’ contributions

PKL, BPK and FFB designed the work, administered and supervised the project, and contributed to the final version of the manuscript, and approved the final version to be published. BLNK, JMTN, LMNN, TEN, VN and YKDM collected, analyzed and interpreted the data, and contributed to the final version of the manuscript, and approved the final version to be published.

Publisher’s note

The Publisher of the Journal remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

[1]

The World Health Organization. Shigella. [Online] Available from: https://www.who.int/teams/immunization-vaccines-and-biologicals/diseases/shigella [Accessed on 4th March 2024].

[2]

Kouitcheu LB, Tamesse JL, Kouam J. The anti-shigellosis activity of the methanol extract of Picralima nitida on Shigella dysenteriae type-induced diarrhoea in rats. BMC Complement Altern Med 2013;13. doi: 10.1186/1472-6882-13-211.

[3]

Matanza XM, Clements A. Pathogenicity and virulence of Shigella sonnei: A highly drug-resistant pathogen of increasing prevalence. Virulence 2023; 14(1). doi: 10.1080/21505594.2023.2280838.

[4]

Bai X, Li X, Liu X, Xing Z, Su R, Wang Y, et al. Antibacterial effect of eugenol on Shigella flexneri and its mechanism. Foods 2022; 11(17). doi: 10.3390/foods11172565.

[5]

Kebede F, Markos M. Does therapeutic zinc level of supplementation for diminutions of acute diarrheal morbidity varied in public and private health institutions in Ethiopia, data from EDHS 2016? Int J Pediatr 2022;2022. doi: 10.1155/2022/9975917.

[6]

Williams P, Berkley J. Dysentery (shigellosis) current who guidelines and the WHO essential medicine list for children. Paediatr Int Child Health 2016;2016.

[7]

Masoumi B, Eslami G, Alizadeh-Navaei R, Mondal P, Rezai MS. Safety profile of using ciprofloxacin inpaediatrics: A systematic review and meta-analysis. J Pediatr 2019; 7(3):129-140.

[8]

Salimiyan Rizi K, Farsiani H, Sasan MS. High rate of resistance to ceftriaxone and azithromycin among Shigella spp. isolates at three children’s referral hospitals in Northeast Iran. J Infect Chemother 2020; 26(9):955.

[9]

Liheluka E, Gibore NS, Lusingu JPA, Gesase S, Minja DTR, Lamshöft M, et al. Medicinal plants for treatment of diarrhoeal diseases among under-five children: Experience from traditional healers in North-eastern Tanzania. BMC Complement Med Ther 2023;23:379. doi: 10.1186/s12906-023-04216-0.

[10]

Nguelo Talla AC, Madiesse Kemgne EA, Ngouana V, Kouamou BLN, Nzeye Ngameni LM, Pinlap BR, et al. Anti-shigellosis activity and mechanisms of action of extracts from Diospyros gilletii stem bark. Drugs Drug Candidates 2024; 3(1):256-274.

[11]

Adzu B, Amos S, Muazzam I, Inyang US, Gamaniel KS. Neuropharmacological screening of Diospyros mespiliformis in mice. J Ethnopharmacol 2002;83:139-143.

[12]

Belemtougri RG, Constantin B, Cognard C, Raymond G, Sawadogo L. Effects of two medicinal plants Psidium guajava L. (Myrtaceae) and Diospyros mespiliformis L. (Ebenaceae) leaf extracts on rat skeletal muscle cells in primary culture. J Zhejiang Univ Sci 2006;B7:56-63.

[13]

Kaikabo AA, Suleiman MM, Samuel BB, Eloff JN. Antibacterial activity of eleven South African plants use in treatment of diarrhoea in folkloric medicine. Afr J Tradit Complement Altern Med 2009;6:315-316.

[14]

Mmongoyo JA, Nair MG, Linz JE, Wu F, Mugula JK, Dissanayake AA, et al. Bioactive compounds in Diospyros mafiensis roots inhibit growth, sporulation and aflatoxin production by Aspergillus flavus and Aspergillus parasiticus. World Mycotoxin J 2017;10:237-248.

[15]

Maridass M. Phytochemicals from genus Diospyros (L.) and their biological activities. Ethnobot Leafl 2008;12:231-244.

[16]

Akak CM, Djama CM, Nkengfack AE, Tu PF, Lei LD. New coumarin glycosides from the leaves of Diospyros crassiflora (Hiern). Fitoterapia 2010;81:873-877.

[17]

Akak CM, Nkengfack AE, Tu PF. Norbergenin derivatives from Diospyros crassiflora (Ebenaceae). Nat Prod Commun 2013;8:1575-1578.

[18]

Tameye JNS. Phytochemical studies of Diospyros gilletii De Wild and Diospyros fragrans Gürke (Ebenaceae), chemical transformations and antibacterial, antioxidant and cytotoxic activities of extracts and isolated compounds. Yaoundé Cameroon: University of Yaounde 1; 2022, p. 289. [Online] Available from: https://savoirs.cames.online/jspui/handle/20.500.12177/11202 [Accessed on 14 February 2024].

[19]

Wambe H, Noubissi PA, Fokam Tagne MA, Foyet Fondjo A, Fankem GO, Kamtchouing I, et al. Anti-shigellosis activity of Cola anomala water/ethanol pods extract on Shigella flexneri-induced diarrhea in rats. Biomed Res Int 2019;2019. doi: 10.1155/2019/6706230.

[20]

Bagamboula CF, Uyttendaele M, Debevere J. Antimicrobial effect of spices and herbs on Shigella sonnei and Shigella flexneri. J Food Prot 2003; 66(4):668-673.

[21]

Pinlap BR, Pone Kamdem B, Kamto EL, Ngouana V, Melogmo Dongmo YK, Lunga PK, et al. Extracts from Cardiospermum grandiflorum and Blighia welwitschii (Sapindaceae) reveal antibacterial activity against Shigella species. S Afr J Bot 2024;164:419-428.

[22]

Tameye NSJ, Akak CM, Happi GM, Frese M, Stammler HG, Neumann B, et al. Antioxidant norbergenin derivatives from the leaves of Diospyros gilletii De Wild (Ebenaceae). Phytochem Lett 2020,36:63-67.

[23]

Liu B, Wang M, Wang X. Phytochemical analysis and antibacterial activity of methanolic extract of Bergenia purpurascens against common respiratory infection causing bacterial species in vitro and in neonatal rats. Microb Pathog 2018;117:315-319.

[24]

Kour H, Raina R, Verma PK, Pankaj NK, Singh SP. Phytochemical ingredients and pharmacological properties of Bergenia ciliata. J Vet Pharmacol Toxicol 2019;18:1-10.

[25]

Nyemb JN, Djankou MT, Talla E, Tchinda AT, Ngoudjou DT, Iqbai J, et al. Antimicrobial, α-glucosidase and alkaline phosphatase inhibitory activities of bergenin, the major constituent of Cissus populnea roots. Med Chem 2018;8:426-430.

[26]

Obasohan PE, Walters SJ, Jacques R, Khatab K. A scoping review of the risk factors associated with anaemia among children under five years in sub-Saharan African countries. Int J Environ Res Public Health 2020; 17(23). doi: 10.3390/ijerph17238829.

[27]

Benrahou K, Mrabti HN, Assaggaf HM, Mortada S, Salhi N, Rouas L, et al. Acute and subacute toxicity studies of Erodium guttatum extracts by oral administration in rodents. Toxins (Basel) 2022; 14(11). doi: 10.3390/toxins14110735.

[28]

Huang HJ, Chou CL, Sandar TT, Liu WC, Yang HC, Lin YC, et al. Currently used methods to evaluate the efficacy of therapeutic drugs and kidney safety. Biomolecules 2023;13. doi: 10.3390/biom13111581.

[29]

Rayego-Mateos S, Marquez-Expósito L, Rodrigues-Diez R, Sanz AB, Guiteras R, Doladé N, et al. Molecular mechanisms of kidney injury and repair. Int J Mol Sci 2022; 23(3). doi: 10.3390/ijms23031542.

[30]

Yang J, Lee S, Chang S, Ko H, Ryu S, Kweon M. A mouse model of shigellosis by intraperitoneal infection. J Infect Dis 2014; 209(2):203-215.

[31]

Nasser A, Mosadegh M, Azimi T, Shariati A. Molecular mechanisms of Shigella effector proteins: A common pathogen among diarrheic pediatric population. Mol Cell Pediatr 2022; 9(1):12. doi: 10.1186/s40348-022-00145-z.

[32]

Gururaja GM, Mundkinajeddu D, Kumar AS, Dethe SM, Allan JJ, Agarwal A. Evaluation of cholesterol-lowering activity of standardized extract of Mangifera indica in Albino Wistar rats. Pharmacognosy Res 2017; 9(1):21-26. doi: 10.4103/0974-8490.199770.

[33]

Nasef NA, Mehta S. Role of inflammation in pathophysiology of colonic disease: An update. Int J Mol Sci 2020;21. doi: 10.3390/ijms21134748.

[34]

Al-Qahtani AA, Alhamlan FS, Al-Qahtani AA. Pro-inflammatory and anti-inflammatory interleukins in infectious diseases: A comprehensive review. Trop Med Infect Dis 2024;9. doi: 10.3390/tropicalmed9010013.

[35]

Gasmi A, Shanaida M, Oleshchuk O, Semenova Y, Mujawdiya PK, Ivankiv Y, et al. Natural ingredients to improve immunity. Pharmaceuticals (Basel) 2023; 16(4). doi: 10.3390/ph16040528.

[36]

Blatkiewicz M, Sielatycka K, Piotrowska K, Kilańczyk E. DHEA and its metabolites reduce the cytokines involved in the inflammatory response and fibrosis in primary biliary cholangitis. Int J Mol Sci 2023;24. doi: 10.3390/ijms24065301.

[37]

Kłósek M, Krawczyk-Łebek A, Kostrzewa-Susłow E, Szliszka E, Bronikowska J, Jaworska D, et al. In vitro anti-inflammatory activity of methyl derivatives of flavanone. Molecules 2023;2023. doi: 10.3390/molecules28237837.

[38]

Di Stasi LC. Coumarin derivatives in inflammatory bowel disease. Molecules 2021; 26(2). doi: 10.3390/molecules26020422.

[39]

Liu W, Cui X, Zhong Y, Ma R, Liu B, Xia Y. Phenolic metabolites as therapeutic in inflammation and neoplasms: Molecular pathways explaining their efficacy. Pharmacol Res 2023; 193. doi: 10.1016/j.phrs.2023.106812.

[40]

Barakat M, Syed NK, Hasen E, Abdulrazzaq SB, Thiab S, Al-Najjar MAA, et al. The effect of natural products on inflammatory cytokines production and secretion. Phytomedicine Plus 2023; 3. doi: 10.1016/j.phyplu.2023.100488.

[41]

Balaji S, Kavasseri Ganesan K. Inhibition of inducible nitric oxide production by Caryota urens and its active constituents umbelliferone and rutin. J Ayurveda Integr Med 2021; 12(2):369-372.

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