TY - JOUR
T1 - Gastroprotective activity of caryophyllene oxide
T2 - The role of nitric oxide, prostaglandins and sulfhydryls
AU - Sánchez-Mendoza, María Elena
AU - Cruz-Antonio, Leticia
AU - Cupido-Sánchez, María Guadalupe
AU - García-Castillo, Guillermo
AU - Arrieta, Jesús
N1 - Publisher Copyright:
© 2014 Sánchez-Mendoza et al.
PY - 2014
Y1 - 2014
N2 - The present study was carried out to evaluate the gastroprotective effect of caryophyllene oxide, and investigate the gastroprotective mechanism. For this purpose, Wistar rats received vehicle, caryophyllene oxide (10-100 mg/kg) or carbenoxolone (1-100 mg/kg, used as the reference drug). Thirty minutes later absolute ethanol was given orally, and 2 h later the stomach was dissected and the damaged area measured. In other experiments, the rats received L-NAME (70 mg/kg, i. p.), indomethacin (10 mg/kg, s. c.), and N-ethylmaleimide (10 mg/kg, s. c.), before the administration of the caryophyllene oxide (100 mg/kg) or carbenoxolone (100 mg/kg). Two control groups were included in these evaluations. Again, thirty minutes later absolute ethanol was given orally, and 2 hours later the animals were sacrificed to measure the ulcer index. Treatment of rats with caryophyllene oxide and carbenoxolone elicited a dose-dependent gastroprotective effect. The gastroprotection observed with the administration of caryophyllene oxide was attenuated in rats pretreated with the inhibitors. This suggests that the gastroprotective mechanism of action of caryophyllene oxide involves NO, prostaglandins and sulfhydryl groups. In the case of carbenoxolone, the partial participation of NO, prostaglandins and sulfhydryls was observed.
AB - The present study was carried out to evaluate the gastroprotective effect of caryophyllene oxide, and investigate the gastroprotective mechanism. For this purpose, Wistar rats received vehicle, caryophyllene oxide (10-100 mg/kg) or carbenoxolone (1-100 mg/kg, used as the reference drug). Thirty minutes later absolute ethanol was given orally, and 2 h later the stomach was dissected and the damaged area measured. In other experiments, the rats received L-NAME (70 mg/kg, i. p.), indomethacin (10 mg/kg, s. c.), and N-ethylmaleimide (10 mg/kg, s. c.), before the administration of the caryophyllene oxide (100 mg/kg) or carbenoxolone (100 mg/kg). Two control groups were included in these evaluations. Again, thirty minutes later absolute ethanol was given orally, and 2 hours later the animals were sacrificed to measure the ulcer index. Treatment of rats with caryophyllene oxide and carbenoxolone elicited a dose-dependent gastroprotective effect. The gastroprotection observed with the administration of caryophyllene oxide was attenuated in rats pretreated with the inhibitors. This suggests that the gastroprotective mechanism of action of caryophyllene oxide involves NO, prostaglandins and sulfhydryl groups. In the case of carbenoxolone, the partial participation of NO, prostaglandins and sulfhydryls was observed.
KW - Caryophyllene oxide
KW - Gastric ulcer
KW - Gastroprotection
KW - Terpenoid
UR - http://www.scopus.com/inward/record.url?scp=84927009712&partnerID=8YFLogxK
U2 - 10.7324/JAPS.2014.40901
DO - 10.7324/JAPS.2014.40901
M3 - Artículo
SN - 2231-3354
VL - 4
SP - 1
EP - 5
JO - Journal of Applied Pharmaceutical Science
JF - Journal of Applied Pharmaceutical Science
IS - 9
ER -