No abstract

Bis[benzyl N'-(indol-3-ylmethylene)-hydraz inecarbodithioatoJ-nickel(lI) (BIHCN) has been used in traditional medicine for their biological activities. The present study was performed to evaluate the anti ulcerogenic activity of BIHCN against ethanol induced gastric mucosal injury in rats. Six groups of adult Sprague Dawley rats were orally pre-treated respectively with 10% Tween 20 solution (ulcer control group), omeprazole 20 mg/kg (reference group), and 50,100,200 and 400 mg/kg of BIHCN in 10% Tween 20 solution (experimental groups) one hour before oral administration of absolute ethanol to generate gastric mucosal injury. After an additional hour, the rats were sacrificed and the ulcer areas of the gastric walls were determined. Grossly, the ulcer control group exhibited severe mucosal injury, whereas pre-treatment with compound exhibited significant protection of gastric mucosal injury. Histological studies of the gastric wall revealed that ulcer control group exhibited severe damage of gastric mucosa; along with edema and leucocytes infiltration of submucosal layer compared to rats pre-treated with BIHCN which showed comparatively gastric mucosal protection, reduction or absence of edema and leucocytes infiltration of submucosal layer. Acute toxicity study of BIHCN with a higher dose of 5 g/kg did not manifest any toxicological signs in rats. In conclusions, the present finding suggests that BIHCN promotes ulcer protection as ascertained grossly by significant reduction of ulcer area, and histologically by comparatively decreases in ulcer areas, reduction or absence of edema and leucocytes infiltration of submucosal layer compared to ulcer control group. ulcer. period of addition of carbon disulfide. To the mixture, 40% ethanol (60 m]) was added and the solution was cooled in ice. Benzyl chloride (25.3 g, 0.2 mol) was then added slowly with vigorous stirring. The white product was separated by filtration, washed with water and dried in air. The crude product was recrystallized from absolute ethanol; yield, 23 g (58%).

Polygonatum odoratum is an important herbal medicine that is used in folk medicine for the treatment of various elements and its components are reported to have various biological effects. This study was conducted to evaluate the effects of topical application of ethanol leaf extract of this plant on the rate of wound healing closure and histology of healed wound. Four groups of male Sprague Dawley rats, all were experimentally wound in the posterior neck area. The animal groups were topically treated respectively with 0.4 ml of each vehicle (gum acacia), Intrasite gel, 100 and 200 mg/ml of ethanol leaf extract. Macroscopically, wound dressed with leaf extracts and Intrasite gel-treated group significantly healed earlier than those treated with vehicle, and the rate of wound healing was significantly accelerated by topical application of 200 mg/kg leaf extract. Histological analysis of healed wounds dresses with leaf extracts showed comparatively less scar width at wound closure and healed wound contained less inflammatory cells and more collagen with angiogenesis as compared to wounds dressed with vehicle. In conclusion, wounds dressed with leaf extracts significantly enhanced the acceleration of wound healing enclosure in rats.

Indolic compounds have attracted a lot of attention due to their interesting biological properties. The present study was performed to evaluate the subacute toxicity and anti-ulcer activity of BClHC against ethanol-induced gastric ulcers. Experimental animal groups were orally pre-treated with different doses of BClHC (50, 100, 200 and 400 mg/kg) in 10% Tween 20 solution (vehicle). Blank and ulcer control groups were pre-treated with vehicle. The positive group was orally pretreated with 20 mg/kg omeprazole. After one hour, all groups received absolute ethanol (5 mL/kg) to generate gastric mucosal injury except the blank control group which was administered the vehicle solution. After an additional hour, all rats were sacrificed, and the ulcer areas of the gastric walls determined. Grossly, the ulcer control group exhibited severe mucosal injury, whereas pre-treatment with either derivative or omeprazole resulted in significant protection of gastric mucosal injury. Flattening of gastric mucosal folds was also observed in rats pretreated with BClHC. Histological studies of the gastric wall of ulcer control group revealed severe damage of gastric mucosa, along with edema and leucocytes infiltration of the submucosal layer compared to rats pre-treated with either BClHC or omeprazole where there were marked gastric protection along with reduction or absence of edema and leucocytes infiltration of the submucosal layer. Subacute toxicity study with a higher dose of derivative (5 g/kg) did not manifest any toxicological signs in rats. In conclusions, the present finding suggests that benzyl N'-(5-chloroindol-3-ylmethylidene)hydrazinecarbodithioate promotes ulcer protection as ascertained by the comparative decreases in ulcer areas, reduction of edema and leucocytes infiltration of the submucosal layer.