bisabolol and Abdominal-Pain

bisabolol has been researched along with Abdominal-Pain* in 1 studies

Other Studies

1 other study(ies) available for bisabolol and Abdominal-Pain

Article	Year
(-)-α-Bisabolol attenuates visceral nociception and inflammation in mice. Fitoterapia, 2011, Volume: 82, Issue:2 The study examined the antiinflammatory and antinociceptive effects of the sesquiterpene (-)-α-bisabolol (BISA). The antiinflammatory effect was evaluated on acute models of dermatitis induced by Croton oil, arachidonic acid, phenol and capsaicin, respectively, in mouse ear. BISA inhibited the dermatitis induced by all noxious agents, except capsaicin. BISA was assessed in two established mouse models of visceral nociception. Mice were pretreated orally with BISA, and the pain-related behavioral responses to intraperitoneal cyclophosphamide or to intracolonic mustard oil were analyzed. BISA showed a dose-unrelated significant antinociception. Collectively, the results suggest that BISA may be an topical antiinflammatory and visceral antinociceptive agent. Topics: Abdominal Pain; Acute Disease; Analgesics; Animals; Anti-Inflammatory Agents; Behavior, Animal; Colon; Cyclophosphamide; Dermatitis; Disease Models, Animal; Ear; Male; Mice; Monocyclic Sesquiterpenes; Mustard Plant; Oils, Volatile; Peritoneum; Plant Extracts; Plant Oils; Sesquiterpenes; Skin	2011

Article

Year

(-)-α-Bisabolol attenuates visceral nociception and inflammation in mice.

Fitoterapia, 2011, Volume: 82, Issue:2

The study examined the antiinflammatory and antinociceptive effects of the sesquiterpene (-)-α-bisabolol (BISA). The antiinflammatory effect was evaluated on acute models of dermatitis induced by Croton oil, arachidonic acid, phenol and capsaicin, respectively, in mouse ear. BISA inhibited the dermatitis induced by all noxious agents, except capsaicin. BISA was assessed in two established mouse models of visceral nociception. Mice were pretreated orally with BISA, and the pain-related behavioral responses to intraperitoneal cyclophosphamide or to intracolonic mustard oil were analyzed. BISA showed a dose-unrelated significant antinociception. Collectively, the results suggest that BISA may be an topical antiinflammatory and visceral antinociceptive agent.

Topics: Abdominal Pain; Acute Disease; Analgesics; Animals; Anti-Inflammatory Agents; Behavior, Animal; Colon; Cyclophosphamide; Dermatitis; Disease Models, Animal; Ear; Male; Mice; Monocyclic Sesquiterpenes; Mustard Plant; Oils, Volatile; Peritoneum; Plant Extracts; Plant Oils; Sesquiterpenes; Skin

2011