The genus Zingiberaceae has been widely used for phytotherapeutic purposes in traditional medicine throughout the world for its anti-inflammatory activity. Experimental studies have established that inflammation caused by chronic infections represents a risk factor for different forms of cancer. The objective of this study was focused on determining the anti-inflammatory capacity and cytotoxic activity of aqueous extracts of Elettaria cardamomum (cardamom) and Curcuma Longa (turmeric). The extracts were obtained by maceration and, through GC-MS/MS, a total of 11 different chemical components were determined in the aqueous extract of cardamom and 7 in the extract of turmeric. The main compounds found in cardamom and turmeric were α-terpinyl acetate (54.46%) and β-turmerone (33.45%), respectively. RT-qPCR results showed significantly lower gene expression levels of innate inflammatory cytokines (IL-6 and TNF-α) compared to the control (LPS). Also, it was observed that the extracts do not possess cytotoxic activity against different cell lines, where E. cardamomum showed EC50 (µg/mL) of 473.84 (HeLa cells), 237.36 (J774A.1 cells), 257.51 (Vero E6 cells), and 431.16 (Balb/C peritoneal cells) and C. longa showed EC50 (µg/mL) of 351.17 (HeLa cells), 430.96 (J774A.1 cells), 396.24 (Vero E6 cells), and 362.86 (Balb/C peritoneal cells). The results of this research suggest that natural extracts of E. cardamomum and C. longa possess anti-inflammatory effects and no cytotoxic activity against HeLa, J774A.1, Vero E6, and Balb/C peritoneal cell lines, Finally, it was observed that the extracts also decreased nitric oxide (NO) production in peritoneal macrophages.
Background:In clinical therapy, there is no satisfactory drug available for treatment of urolithiasis, especially for the prevention of their recurrence. The aim of this work was to evaluate in vivo antiurolithic activity of methanolic extract of Berberis trifoliata leaves. Material and methods: Urolithiasis was induced in Wistar rats by zinc disc implantation in urinary bladder. Upon postsurgical recovery, different doses of the methanolic extract of B. trifoliata leaves (50, 100 and 150 mg/kg body weight) were administered orally to zinc disc implanted rats for a period of 20 days. Antiurolithiatic activity was evaluated by measuring the difference between the weight of the implanted zinc discs at the time of implantation and the final weight of the dried calculi taken out from the bladder at the end of the 20 days period of treatment. Results: Extract of B. trifoliata significantly reduced calculi deposition around the implanted zinc disc at all doses (50, 100, and 150 mg/kg). Conclusion: Treatment with methanolic extract of B. trifoliata is useful agent against the kidney stone formation.
The usefulness of traditional plants in Mexico to treat human ailments has been known since ancient times. This work evaluated the antimicrobial, anticoagulant, antioxidant, cytotoxic, and anti-inflammatory potential of ethanolic extracts of Aloe vera, Equisetum arvense, Mimosa tenuiflora, Lippia graveolens, and Syzygium aromaticum. The antimicrobial activity of the extracts was evaluated against Streptococcus mutans and Streptococcus sorbinus; a significant inhibitory effect of the L. graveolens extract on both bacteria was observed at concentration levels of 250 µg/mL and greater. The anticoagulant activity was evaluated in terms of prothrombin time (PT) and activated partial thromboplastin time (APTT), A. vera and M. tenuiflora extracts showed no significant difference (p ˂ 0.05) in PT compared with the control, and for APTT the extracts of A. vera, L. graveolens, and S. aromaticum decreased the APTT significantly (p ˂ 0.05) compared with the control. The antioxidant potential by DPPH assay indicated that the E. arvense extract behaved statistically the same as the control. The cytotoxic activity was evaluated in HGF-1 cells using the fluorometric microculture cytotoxicity assay technique, and none of the extracts was toxic at 125 and 250 µg/mL concentrations. Finally, the anti-inflammatory activity was evaluated using ELISA, where the A. vera extract showed the best anti-inflammatory capacity. Further research on the search for bioactive metabolites and elucidation of action mechanisms of the most promising extracts will be carried out.
Introduction: In tropical and developing countries, pathogenic protozoa are a major public health problem. Objective: The main objective of this study was the evaluation of ethanol extracts of Curcuma longa and Berberis vulgaris, as well as their main components curcumin (Cur) and berberine (Ber) in non-encapsulated form and encapsulated into polymeric nanoparticles (NPs) on Entamoeba histolytica and Trichomonas vaginalis trophozoites as well as to evaluate the hemolytic activity. Additionally, we studied the morphology of the NPs, average particle size, polydispersity index (PDI), and encapsulation percentages (%EE) of the formulations. Methods: For this purpose, the activity of the encapsulated and non-encapsulated treatments against E. histolytica and T. vaginalis was evaluated by the microassay technique (in-vitro). In addition, the cytotoxic capacity was determined by the hemolysis technique in healthy erythrocytes. The size and morphology of the NPs were determined by photon correlation spectroscopy and scanning electron microscopy (SEM). Results: Phytochemical analysis of the extracts showed that C. longa had mainly tannins, phenols and flavonoids, and B. vulgaris alkaloids. The NPs were significantly (P < 0.001) more effective compared to their non-encapsulated counterparts, but CurNPs and BerNPs were the most efficient treatments. CurNPs showed IC50 values (μg/mL) of 9.48 and 4.25, against E. histolytica and T. vaginalis respectively, and BerNPs 0.24 and 0.71. The respective particle sizes and encapsulation percentages for CurNPs and BerNPs were 66.5 and 73.4 nm, 83.59 and 76.48 %, respectively. SEM shows that NPs had a spherical morphology. Finally, we analyzed whether ethanolic extracts and NPs induced hemolytic activity and found that significantly NPs reduced hemolysis compared to the non-encapsulated extracts. Conclusions: Therefore, these findings suggest that the use of NPs represent a valuable and novel source of administration of bioactive compounds for the therapeutic treatment of diseases caused by protozoa of clinical interest since they potentiate the amebicidal and trichomonicidal activity of the administered products without significant hemolytic activity.
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