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  • ThesisItemOpen Access
    EVALUATION OF ANTI-INFLAMMATORY ACTIVITY AND SAFETY PROFILE OF ALCOHOLIC STEM-BARK EXTRACT OF Boswellia ovalifoliolata IN RATS
    (Sri Venkateswara Veterinary University, TIRUPATI – 517 502,A.P, 2009-10) SAKUNTHALA DEVI, P.R; ADILAXMAMMA, K (Major); SRINIVASA RAO, G; SRILATHA, Ch
    ABSTRACT : Experimental studies were conducted on the ameliorating effect of alcoholic stem-bark extract of Boswellia ovalifoliolata in acute and chronic models of inflammation and the pharmacological actions were compared to those of diclofenac in rats. The safety of B. ovalifoliolata was also studied in a sub-acute toxicity model in rats using 3 different dose levels viz., 100, 500 and 1000 mg/Kg body weight. Carrageenan-induced inflammation was evaluated in four groups comprising of six rats in each. Group 1 was given normal saline, groups 2, 3 and 4 were respectively given carrageenan + 0.3 % CMC p.o, carrageenan + 18 diclofenac (10 mg/Kg p.o) and carrageenan + alcoholic extract of B. ovalifoliolata (100 mg/Kg p.o). The carrageenan significantly increased hind paw edema in group 2 which was significantly (P<0.05) reduced in groups 3 and 4 (64 and 70 % respectively). The activity of ALT, AST and acid phosphatase showed significant (P<0.05) elevation following carrageenan-induced inflammation in group 2, but was significantly (P<0.05) decreased in groups 3 and 4. There was no change in total protein concentration. In Cotton pellet granuloma study, four groups comprising of six rats in each were utilized; group 1 was given normal saline, groups 2, 3 and 4 were induced cotton pellet granuloma and respectively given 0.3 % CMC p.o, diclofenac (10 mg/Kg p.o) and alcoholic extract of B. ovalifoliolata (100 mg/Kg p.o) for 10 days. The mean weight of granuloma (mg) was significantly (P<0.05) high in group 2. Groups 3 and 4 produced a significant (P<0.05) reduction (40 and 35 %, respectively) in granuloma weight. The activity of ALT, AST, acid phosphatase and GGT, and the concentration of TBARS were significantly (P<0.05) elevated, while the concentration of GSH was significantly (P<0.05) reduced in group 2 as compared to groups 1, 3 and 4. The total protein concentration did not change in any of the groups. Examination of gastric mucosa revealed neither ulceration nor haemorrhages in treatment groups. Safety profile of alcoholic stem-bark extract of B. ovalifoliolata was investigated in four groups comprising of six rats in each were utilized; group 1 was given normal saline, groups 2, 3 and 4 were respectively given alcoholic extract of B. ovalifoliolata @ 100, 500 and 1000 mg/Kg orally for 28 days. The mean activity of AST, ALT and CPK, and the concentration of serum creatinine, total protein, TBARS and GSH did not differ significantly among the groups. There were no clinical signs of abnormality nor gastric erosion and haemorrhage in any group. Weekly body weights, organ weights and haematological parameters did not vary significantly amongst the groups. Histological abnormalities of toxicological significance were not detected on microscopy in 100 mg and 500 mg/Kg b.wt treated groups. However mild histopathological alterations were observed in higher dose group. The per cent stabilization (42.11 and 40.15) exhibited by diclofenac and alcoholic extract did not differ significantly. In conclusion, the present study revealed that the alcoholic stem-bark extract of B. ovalifoliolata has significant anti-inflammatory actions in both acute and chronic inflammation models in rats and the activity was comparable to that of diclofenac in both the models. The safety study on alcoholic stem-bark extract of B. ovalifoliolata revealed mild histopathological changes in higher dose group on sub-acute toxicity study in rats.