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DOI: 10.1055/s-0037-1608136
Anti-inflammatory and anti-tubercular properties screening of natural products from Plectranthus species
Publication History
Publication Date:
24 October 2017 (online)
Medicinal plants of the Plectranthus genus are widely used in traditional medicine for their anti-inflammatory and anti-infective properties [1]. Previous reports [2,3] directed this study for the production and release of Nitric Oxide, and for the CFU analysis of Mycobacterium tuberculosis H37Rv (Mtb) growth inhibition, of Plectranthus spp. non-cytotoxic compounds.
The natural compounds isolated from Plectranthus spp. using bioassay-guided fractionation of extracts, were: 6β,7α-dihydroxyroyleanone and 6,7-dehydroroyleanone (P. madagascariensis); β-sitosterol, stigmasterol, oleanolic and ursolic acids (P. ecklonii); (13S,15S)-6β,7α,12α,19-tetrahydroxy-13β,16-cyclo-8-abietene-11,14-dione (P. porcatus); (11R*,13E)-11-acetoxyhalima-5,13-dien-15-oic acid, Plectrornatin C, 1,6-di-O-acetylforskolin and 1,6-di-O-acetyl-9-deoxyforskolin (P. ornatus); α-amyrin and β-amyrin (P. neochilus); chlorogenic acid (P. saccatus) and rosmarinic acid (all aqueous extracts).
The compounds were unable to reveal in vitro anti-inflammatory activity neither in LPS-stimulated RAW 264.7 cells nor in the S-nitroso-N-acetylpenicillamine assay. Nonetheless, regarding the Mtb growth inhibition, one semi-synthetic halimane derivative (11R*,13E)-halima-5,13-diene-11,15-diol) previously prepared [4], revealed promising results (2.1 × 105 CFU/mL), with an effect similar to the anti-tubercular drugs ethambutol (2.0 × 105 CFU/mL) and isoniazid (1.2 × 105 CFU/mL).
To the best of our knowledge, this report is the first scientific validation on Plectranthus spp. isolated compounds concerning their anti-inflammatory activity for NO production and release, and concerning their anti-mycobacterial activity for Mtb growth inhibition. Further studies regarding other inflammatory mediators are under study.
[1] Lukhoba CW, Simmonds MS, Paton AJ. J. Ethnopharmacol 2006; 103: 1 – 24;
[2] Rijo, P, Simões MF, Francisco AP, Rojas R, Gilman RH, Vaisberg AJ, Rodríguez B, Moiteiro C. Chem. Biodivers 2010; 7: 922 – 932;
[3] Rijo, P, Gaspar-Marques C, Simões MF, Jimeno ML, Rodríguez B. Biochemical Systematics and Ecology 2007; 35: 215 – 221.
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