TY - JOUR
T1 - Pharmacological interaction of α-bisabolol and diclofenac on nociception, inflammation, and gastric integrity in rats
AU - Ortiz, Mario I.
AU - Cariño-Cortés, Raquel
AU - Ponce-Monter, Héctor A.
AU - Castañeda-Hernández, Gilberto
AU - Chávez-Piña, Aracely Evangelina
N1 - Publisher Copyright:
© 2017 Wiley Periodicals, Inc.
PY - 2018/2
Y1 - 2018/2
N2 - (Table presented.). The combination of nonsteroidal anti-inflammatory drugs (NSAIDs) with herbal products having analgesic and anti-inflammatory effects may increase their beneficial effects and limit their side effects. In this study, the effects of an interaction between α-bisabolol and the NSAID, diclofenac on nociception (formalin test), inflammation (paw inflammation produced by carrageenan) and gastric injury in rat was assessed. Diclofenac, α-bisabolol, or diclofenac–α-bisabolol combinations produced antinociceptive and anti-inflammatory effects in rat (p <.05). The systemic administration of diclofenac, but not α-bisabolol, produced gastric damage while the diclofenac–α-bisabolol combinations produced limited gastric damage. Effective dose (ED40) values were determined for each individual drug and analyzed isobolographically. The theoretical ED40 values for the antinociceptive (98.89 mg/kg) and the anti-inflammatory (41.2 mg/kg) effects differed from the experimental ED40 values (antinociception: 38.7 mg/kg and anti-inflammation: 13.4 mg/kg). We concluded that the interactions between diclofenac and α-bisabolol are synergistic. These data suggest that the diclofenac–α-bisabolol combinations can interact to produce minor gastric damage, thereby offering a safer therapeutic alternative for the clinical management of inflammation and/or inflammatory pain.
AB - (Table presented.). The combination of nonsteroidal anti-inflammatory drugs (NSAIDs) with herbal products having analgesic and anti-inflammatory effects may increase their beneficial effects and limit their side effects. In this study, the effects of an interaction between α-bisabolol and the NSAID, diclofenac on nociception (formalin test), inflammation (paw inflammation produced by carrageenan) and gastric injury in rat was assessed. Diclofenac, α-bisabolol, or diclofenac–α-bisabolol combinations produced antinociceptive and anti-inflammatory effects in rat (p <.05). The systemic administration of diclofenac, but not α-bisabolol, produced gastric damage while the diclofenac–α-bisabolol combinations produced limited gastric damage. Effective dose (ED40) values were determined for each individual drug and analyzed isobolographically. The theoretical ED40 values for the antinociceptive (98.89 mg/kg) and the anti-inflammatory (41.2 mg/kg) effects differed from the experimental ED40 values (antinociception: 38.7 mg/kg and anti-inflammation: 13.4 mg/kg). We concluded that the interactions between diclofenac and α-bisabolol are synergistic. These data suggest that the diclofenac–α-bisabolol combinations can interact to produce minor gastric damage, thereby offering a safer therapeutic alternative for the clinical management of inflammation and/or inflammatory pain.
KW - diclofenac
KW - gastric damage
KW - inflammation
KW - nociception
KW - α-bisabolol
UR - http://www.scopus.com/inward/record.url?scp=85037997148&partnerID=8YFLogxK
U2 - 10.1002/ddr.21418
DO - 10.1002/ddr.21418
M3 - Artículo
SN - 0272-4391
VL - 79
SP - 29
EP - 37
JO - Drug Development Research
JF - Drug Development Research
IS - 1
ER -