Buddleja thyrsoides Lam. crude extract presents antinociceptive effect on an arthritic pain model in mice

Biochem J. 2017 Aug 17;474(17):2993-3010. doi: 10.1042/BCJ20170008.

Abstract

Arthritis is a chronic inflammatory disease which reduces the life quality of affected individuals. Therapeutic tools used for treating inflammatory pain are associated with several undesirable effects. Buddleja thyrsoides Lam., known as 'Barbasco' or 'Cambara', is mostly used in several disorders and possesses antirheumatic, anti-inflammatory, and analgesic properties. Here, we investigated the antinociceptive and anti-inflammatory effects of the B. thyrsoides crude extract applied orally and topically in acute pain models and an arthritic pain model induced by complete Freund's adjuvant (CFA) paw injection in male mice (25-30 g). The high-performance liquid chromatography (HPLC) of the B. thyrsoides extract crude revealed the presence of the lupeol, stigmasterol, and β-sitosterol. The stability study of the B. thyrsoides gel did not show relevant changes at low temperatures. The oral treatment with the B. thrysoides extract prevented the capsaicin-induced spontaneous nociception and the acetic acid-induced abdominal writhing, but did not alter the thermal threshold in the tail immersion test. The B. thyrsoides antinociceptive effect was not reversed by naloxone in the capsaicin test. The B. thyrsoides oral or topical treatment reversed the CFA-induced mechanical allodynia and thermal hyperalgesia with maximum inhibition (Imax) of 69 ± 6 and 68 ± 5% as well as 78 ± 15 and 87 ± 12%, respectively. Moreover, the topical but not oral treatment inhibited the CFA-induced cell infiltration, but did not reduce the paw edema significantly. The oral treatment with B. thyrsoides did not cause adverse effects. These findings suggest that the oral or topical treatment with B. thyrsoides presents antinociceptive actions in an arthritic pain model without causing adverse effects.

Keywords: Barbasco; Cambará; arthritis; inflammation; nociception; pain.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Pain / drug therapy
  • Administration, Cutaneous
  • Administration, Oral
  • Analgesics, Non-Narcotic / administration & dosage
  • Analgesics, Non-Narcotic / adverse effects
  • Analgesics, Non-Narcotic / chemistry
  • Analgesics, Non-Narcotic / therapeutic use*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / administration & dosage
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Arthritis, Experimental / drug therapy*
  • Brazil
  • Buddleja / chemistry*
  • Buddleja / growth & development
  • Drug Stability
  • Drug Storage
  • Ethnopharmacology
  • Gels
  • Hot Temperature / adverse effects
  • Male
  • Mice
  • Pentacyclic Triterpenes / administration & dosage
  • Pentacyclic Triterpenes / adverse effects
  • Pentacyclic Triterpenes / analysis
  • Pentacyclic Triterpenes / therapeutic use
  • Plant Extracts / administration & dosage
  • Plant Extracts / adverse effects
  • Plant Extracts / chemistry
  • Plant Extracts / therapeutic use*
  • Plant Leaves / chemistry*
  • Plant Leaves / growth & development
  • Sitosterols / administration & dosage
  • Sitosterols / adverse effects
  • Sitosterols / analysis
  • Sitosterols / therapeutic use
  • Stigmasterol / administration & dosage
  • Stigmasterol / adverse effects
  • Stigmasterol / analysis
  • Stigmasterol / therapeutic use
  • Viscosity

Substances

  • Analgesics, Non-Narcotic
  • Anti-Inflammatory Agents, Non-Steroidal
  • Gels
  • Pentacyclic Triterpenes
  • Plant Extracts
  • Sitosterols
  • gamma-sitosterol
  • Stigmasterol
  • lupeol