Main Article Content

Yanti Rahayu
Nuzulia Irawati

Page: 2383-2391

Abstract

Introduction: Blastocystis sp. infection is a prevalent cause of gastrointestinal disorders, contributing to acute diarrhea through inflammatory mechanisms and intestinal mucosal damage. Although metronidazole remains the standard antiparasitic therapy, its use is constrained by side effects and variable efficacy, underscoring the need for safer and more effective alternative treatments derived from natural sources. Mimosa pudica is known to contain bioactive compounds, including flavonoids, tannins, saponins, and alkaloids, which exhibit antiparasitic and anti-inflammatory activities. Objective: This study aims to evaluate the effect of Mimosa pudica leaf extract on reducing parasite numbers in a Wistar rat model of acute diarrhea induced by Blastocystis sp. Methods: Leaf extracts were prepared using ethanol as a solvent and were characterized using Fourier Transform Infrared (FTIR) spectroscopy and phytochemical screening. An in vivo test was conducted in 40 male Wistar rats, divided into six groups: a negative control, a positive control, two metronidazole-treated groups (9 and 13.9 mg), and two extract-treated groups (40 and 80 mg). The primary parameters observed included parasite count in fecal samples, stool consistency, and motor activity. Results: Phytochemical analysis confirmed the presence of flavonoids, tannins, saponins, and alkaloids in the extract. FTIR spectra revealed functional groups such as hydroxyl (–OH), carbonyl (C=O), and aliphatic groups (C–H), which are characteristic of bioactive polyphenolic compounds. In vivo results demonstrated that Mimosa pudica extract significantly reduced Blastocystis sp. burden and improved clinical conditions, including stool consistency, in a dose-dependent manner. The 80 mg dose exhibited the highest efficacy, with 80% of samples becoming parasite-free by day 7 of treatment. Conclusion: The findings indicate that Mimosa pudica extract exhibits significant antiparasitic activity against Blastocystis sp. and shows potential as a therapeutic agent for treating protozoan infections, particularly in the context of acute diarrhea. Further research is warranted to elucidate the precise molecular mechanisms and to evaluate its safety and clinical applicability.

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How to Cite
Rahayu, Y., & Irawati, N. (2026). Effectiveness of Mimosa pudica Extract on Reducing the Number of Blastocystis sp. in Wistar Rats with Acute Diarrhea Model. Journal of Pharmaceutical and Sciences, 9(3), 2383–2391. https://doi.org/10.36490/journal-jps.com.v9i3.1548
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Original Articles

References

. Jadallah KA, Nimri LF, Ghanem RA. Protozoan parasites in irritable bowel syndrome: A case-control study. World journal of gastrointestinal pharmacology and therapeutics. 2017 Nov 6;8(4):201. DOI: https://doi.org/10.4292/wjgpt.v8.i4.201

. Pawelec-Pęciak O, Łanocha-Arendarczyk N, Grzeszczak K, Kosik-Bogacka D. The Role of Blastocystis spp. in the Etiology of Gastrointestinal and Autoimmune Diseases. Pathogens. 2025 Mar 25;14(4):313. DOI: https://doi.org/10.3390/pathogens14040313

. Wijaksana I Ketut Eka, Ernawati DS, Rantam FA, Sudiana IK, Prabowo GI, Notobroto HB. Evaluating the antibacterial potency of Phyllanthus niruri L. leaf extract against oral pathogenic bacteria. J Int Dent Med Res. 2024;17(3):1035–1040.

. Mao X, Wu Ling, Guo Hao, Chen Wei, Cui Yu, Qi Qiong, Li Shilin, Liang Weiguo, Yang Guanghong, Shao Jincheng. The genus Phyllanthus: An ethnopharmacological, phytochemical, and pharmacological review. Journal of Ethnopharmacology. 2016. DOI: https://doi.org/10.1155/2016/7584952

. Asaduzzaman Md, Nahar Lutfun, Biswas Mohammad Shahangir, Podder Munna Kumar, Rahman Md Matiar. Phyllanthus amarus as a multifunctional medicinal herb: Bioactive compounds, mechanisms, and clinical perspectives. Pharmacological Research – Modern Chinese Medicine. 2026. DOI: https://doi.org/10.1016/j.prmcm.2026.100752

. Matou Mélissa, Bercion Sylvie, Merciris Patrick, Meyssonier Nicole, Fernand Déborah, Marianne-Pepin Thérèse. Étude de la composition chimique et du potentiel pharmacologique associé de Phyllanthus amarus. 2018.

. Wijaksana I Komang Evan, Siswanto Olivia Bambang, Pinatih Made Talitha Suryaningsih, Evaluating the Antibacterial Potency of Phyllanthus niruri L. Leaf Extract Against Aggregatibacter actinomycetemcomitans and Porphyromonas gingivalis. 2024. 17.3.1035-1040

. Ndanusa Abdullahi Hassan, Karunakaran Rohini, Abdulmumin Suleiman. A review of the pharmacological and traditional properties of Mimosa pudica. International Journal of Pharmacy and Pharmaceutical Sciences. 2019;11(3):12–16. DOI: https://doi.org/10.22159/ijpps.2019v11i3.30452

. Alam F, Alam R, Yusuf A, et al. Phytochemical screening and neuro-pharmacological activity of Mimosa pudica flowers: Integrating in vitro, in silico, and in vivo approaches. Heliyon. 2025;11(3): e42017. DOI: https://doi.org/10.1016/j.heliyon.2025.e42017

. Mandal Akash Kumar, Pandey Ashok, Sah Ram Kumar, Baral Anil, Sah Prakash. In vitro antioxidant and antimicrobial potency of Mimosa pudica of the Nepalese Terai region: insight into L-mimosine as an antibacterial agent. Evidence-Based Complementary and Alternative Medicine. 2022;2022:6790314. DOI: https://doi.org/10.1155/2022/6790314

. Joseph Blessy, Pradeep R, Suresh Kumar R, Jeeva S. Mimosa pudica Linn.: A comprehensive review on its phytochemistry, pharmacological activities, and mechanisms of action. International Journal of Pharmaceutical Sciences Review and Research. 2013;21(1):234–238.

. Karthikeyan M, Deepa K, Babu PS, Pandurangan A, Suresh Kumar R. Mimosa pudica Linn.: A comprehensive review on its phytochemistry, pharmacological properties, and therapeutic applications. Journal of Drug Delivery and Therapeutics. 2019;9(4):900–906.

. Rizwan K, Majeed I, Bilal M, et al. Phytochemistry and diverse pharmacology of the genus Mimosa: A review. Biomolecules. 2022;12(1):83. DOI: https://doi.org/10.3390/biom12010083

. Panche AN, Diwan AD, Chandra SR. Flavonoids: An overview. J Nutr Sci. 2016;5: e47. DOI: https://doi.org/10.1017/jns.2016.41

. Singh P, Kim YJ, Zhang D, Yang DC. Biological synthesis of nanoparticles from plants and microorganisms. Trends Biotechnol. 2016;34(7):588-599. DOI: https://doi.org/10.1016/j.tibtech.2016.02.006

. Madaniyah L, Fiddaroini S, Hayati EK, et al. Biosynthesis, characterization, and in vitro anticancer effect of plant-mediated silver nanoparticles using Acalypha indica Linn: In silico approach. OpenNano. 2024; 21:100220. DOI: https://doi.org/10.1016/j.onano.2024.100220

. Becker C, Animal models in gastrointestinal research. Gut Microbes. 2022;14(1):2018901.

. Fahim M, Shahzaib A, Nishat N, et al. Plant-based bioactive compounds as therapeutic agents. JCIS Open.2024;16:100125. DOI: https://doi.org/10.1016/j.jciso.2024.100125

. Goli, A. H. (2021). Phytochemical analysis and biological activities of Mimosa pudica. Journal of Herbal Medicine, 27, 100432.

. Rahman, M. M. (2021). Anti-inflammatory effects of plant phenolics in gastrointestinal disorders. Biomedicine & Pharmacotherapy, 139, 111588.

. Verma, P. (2022). Antioxidant and therapeutic potential of Mimosa pudica: A review. Journal of Ethnopharmacology, 285, 114890.

. Upcroft, P., & Upcroft, J. A. (2021). Drug targets and mechanisms of resistance in anaerobic protozoa. Clinical Microbiology Reviews, 34(2), e00132-19.