4.6 Article

Blutaparon portulacoidesethanolic extract reduced IL-1β and inflammatory parameters induced by theMycobacterium complexand carrageenan in mice

Journal

INFLAMMOPHARMACOLOGY
Volume 29, Issue 2, Pages 439-450

Publisher

SPRINGER BASEL AG
DOI: 10.1007/s10787-020-00752-0

Keywords

Amaranthaceae; Blutaparon portulacoides; Inflammation; Mycobacterium tuberculosis

Funding

  1. FAPESP-Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [15/03,726-8, 06/06,079-4]

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The study demonstrates the anti-inflammatory and antibiotic properties of ethanolic extracts obtained from Blutaparon portulacoides stem, suggesting the potential development of safe new drugs with dual anti-inflammatory/antimycobacterial activities.
Information on the health benefits of ethanolic extracts obtained fromBlutaparon portulacoidesstem (EEBP) hasn ' t been consistently described in the literature until the present moment. This study investigated the antimycobacterial, anti-inflammatory and toxicological effects of EEBP in models of inflammation/infection, as well as its chemical composition. Chemical analysis of EEBP by electrospray ionization-mass spectrometry/HPLC-MS/MS identified 3,5,3 '-Trihydroxy-4 '-methoxy-6,7-methylenedioxy-flavone, gomphrenol, ferulic, vanillic, and caffeic acids. The minimum inhibitory concentration of EEBP and isoniazid in the presence ofMycobacterium tuberculosiswas 123.4 and 0.030 mu g/ml, respectively. EEBP oral administration (p.o.) (300-1000 mg/kg) or dexamethasone subcutaneous injection (s.c.) (1 mg/kg) significantly inhibited leukocytes and proteins resulting from carrageenan-induced pleurisy inSwissmice. In the BCG-induced pleurisy model, the oral treatments performed once a day for 7 days, with EEBP (30 and 100 mg/kg) and isoniazid (25 mg/kg), inhibited the increase in plasmatic IL-1 beta levels and in pleural exudate from C57BL-6 mice, and reducedM. tuberculosisgrowth in organs (colony forming units assays). EEBP (30-300 mg/kg, p.o.) and dexamethasone (1 mg/s.c.) significantly prevented carrageenan-induced oedema and mechanical hyperalgesia inSwissmice. The treatments (once a day for 22 days) with EEBP (30 mg/kg, p.o.) and dexamethasone (1 mg/s.c.) substantially inhibited oedema and mechanical- and cold-hyperalgesia at 11, 16 and 22 days after the administration of Freund's Complete Adjuvant in C57bL6 mice. No evidence of physio-pathologic was observed inWistarrats acutely treated with EEBP (2000 mg/kg, p.o.). This study confirms the anti-inflammatory and antibiotic properties of EEBP, opening possibilities for the development of safe new drugs with dual anti-inflammatory/antimycobacterial activities which could be favorable from a pharmacoeconomic perspective.

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