TY - JOUR
T1 - Role of prostaglandins, nitric oxide, sulfhydryls and capsaicin-sensitive neurons in gastroprotection of stigmasterol and β-sitosterol
AU - Sánchez-Mendoza, María Elena
AU - Arrieta, Jesús
AU - Navarrete, Andrés
PY - 2008
Y1 - 2008
N2 - In this investigation the gastroprotective activity of stigmasterol and β-sitosterol was evaluated. Gastric mucosal damage was induced in rats by intragastric ethanol (1 mL/rat). Rats treated orally with stigmasterol suspended in Tween 80 at 10, 30, 100 and 300 mg kg-1 showed 26.2, 39.6, 58.3 and 70.7% gastroprotection, respectively. β-Sitosterol at 10, 30,100 and 300 mg kg-1 showed 21.6, 42.5, 48.5 and 71.2% gastroprotection, correspondingly. The gastroprotection observed at 30 mg kg-1 for stigmasterol and β-sitosterol was attenuated in rats pretreated with indomethacin, (10 mg kg-1, s. c.), NG-nitro-L-arginine methyl ester (L-NAME, 70 mg kg-1, i. p.) and capsaicin (125 mg kg-1, s. c), suggesting that the gastroprotective mechanism of these sterols involves, at least in part, the participation of prostaglandins, nitric oxide (NO) and capsaicin-sensitive sensory neurons (CPSN). The gastroprotection of β-sitosterol was also attenuated by the pretreatment with N-ethylmaleimide (NEM, 10 mg kg-1, s. c.) indicating that endogenous sulfrydryls may be involved in the gastrorpotection of this compound. Carbenoxolone was used as a gastroprotective model drug and showed a dose-dependent gastroprotective effect (25.7, 33.6 and 88.3% of gastroprotection, at 3, 10 and 30 mg kg-1, respectively). The partial participation of PGs, sulfhydryls and NO was observed in the gastroprotective mechanism of carbenoxolone.
AB - In this investigation the gastroprotective activity of stigmasterol and β-sitosterol was evaluated. Gastric mucosal damage was induced in rats by intragastric ethanol (1 mL/rat). Rats treated orally with stigmasterol suspended in Tween 80 at 10, 30, 100 and 300 mg kg-1 showed 26.2, 39.6, 58.3 and 70.7% gastroprotection, respectively. β-Sitosterol at 10, 30,100 and 300 mg kg-1 showed 21.6, 42.5, 48.5 and 71.2% gastroprotection, correspondingly. The gastroprotection observed at 30 mg kg-1 for stigmasterol and β-sitosterol was attenuated in rats pretreated with indomethacin, (10 mg kg-1, s. c.), NG-nitro-L-arginine methyl ester (L-NAME, 70 mg kg-1, i. p.) and capsaicin (125 mg kg-1, s. c), suggesting that the gastroprotective mechanism of these sterols involves, at least in part, the participation of prostaglandins, nitric oxide (NO) and capsaicin-sensitive sensory neurons (CPSN). The gastroprotection of β-sitosterol was also attenuated by the pretreatment with N-ethylmaleimide (NEM, 10 mg kg-1, s. c.) indicating that endogenous sulfrydryls may be involved in the gastrorpotection of this compound. Carbenoxolone was used as a gastroprotective model drug and showed a dose-dependent gastroprotective effect (25.7, 33.6 and 88.3% of gastroprotection, at 3, 10 and 30 mg kg-1, respectively). The partial participation of PGs, sulfhydryls and NO was observed in the gastroprotective mechanism of carbenoxolone.
KW - Gastroprotective effect
KW - Peptic ulcer
KW - Phytosterols
KW - Stigmasterol
KW - Vegetarian diet
KW - β-sitosterol
UR - http://www.scopus.com/inward/record.url?scp=70450221990&partnerID=8YFLogxK
U2 - 10.1177/1934578x0800300406
DO - 10.1177/1934578x0800300406
M3 - Artículo
SN - 1934-578X
VL - 3
SP - 505
EP - 510
JO - Natural Product Communications
JF - Natural Product Communications
IS - 4
ER -