Investigation of anti-inflammatory and antinociceptive activities of trans-dehydrocrotonin, a 19-nor-clerodane diterpene from Croton cajucara. Part 1

Planta Med. 1996 Oct;62(5):402-4. doi: 10.1055/s-2006-957925.

Abstract

The anti-inflammatory and antinociceptive effects of trans-dehydrocrotonin, isolated from the bark of Croton cajucara (Euphorbiaceae), were investigated using several animal models. The trans-dehydrocrotonin produced a significant inhibition of carrageenin-induced paw edema and cotton pellet granuloma in rats. It also inhibited the writhings in mice induced by acetic acid, but did not show a significant effect in the hot-plate test in mice. The LD50 of t-DCTN was 555.0 mg/kg (p.o.) for mice.

MeSH terms

  • Analgesics / isolation & purification
  • Analgesics / pharmacology*
  • Analgesics / toxicity
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / isolation & purification
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Anti-Inflammatory Agents, Non-Steroidal / toxicity
  • Brazil
  • Diterpenes / isolation & purification
  • Diterpenes / pharmacology*
  • Diterpenes / toxicity
  • Diterpenes, Clerodane*
  • Granuloma
  • Lethal Dose 50
  • Male
  • Mice
  • Morphine / pharmacology
  • Pain
  • Plants, Medicinal*
  • Rats
  • Rats, Wistar

Substances

  • Analgesics
  • Anti-Inflammatory Agents, Non-Steroidal
  • Diterpenes
  • Diterpenes, Clerodane
  • dehydrocrotonin
  • Morphine