Alteration of microbiota is related with rheumatoid arthritis (RA) and administration of certain probiotics showed an improvement in RA. The present study was designed to find out the anti-arthritic activity of cell wall content of Lactobacillus plantarum in complete Freund's adjuvant (CFA)-induced arthritis in rats. Freund's adjuvant was injected into the left footpad in female rats on day 0 and dexamethasone (1 mg kg, s.c.) & cell wall content of L. plantarum (10, 10, and 10 cfu/animal, s.c.) treatment were given from day 7 to 21. The change in body weight, paw volume and arthritic index, joint stiffness, gait test, mobility test, erythrocyte sedimentation rate (ESR), serum C-reactive protein (CRP) level, serum rheumatoid factor (RF), and serum TNF-α was measured on day 21. Cell wall content of L. plantarum treated animals showed improvement in all the parameters as compared to that in CFA-treated animals and exert anti-arthritic activity.
In the present study, the immunomodulatory activity and the mechanism of action of the n-butanol fraction (100 mg/kg body weight, per os, once daily for 22 consecutive days) of the root bark of Oroxylum indicum, vent. (Bignoniaceae) was evaluated in rats using measures of immune responses to sheep red blood cells (SRBC haemagglutinating antibody [HA] titer) and delayed-type hypersensitivity (DTH) reactions. In response to SRBC, treatment with the n-butanol fraction caused a significant rise in circulating HA titers during secondary antibody responses, indicating a potentiation of certain aspects of the humoral response. The treatment also resulted in a significant rise in paw edema formation, indicating increased host DTH response. Additionally, the antioxidant potential of the drug was exhibited by significant reductions in whole blood malondialdehyde (MDA) content along with a rise in the activities/levels of superoxide dismutase (SOD), catalase (CAT) and reduced glutathione (GSH). Furthermore, histopathologic analysis of lymphoid tissues showed an increase in cellularity, e.g., T-lymphocytes and sinusoids, in the treatment group. In contrast, dexamethasone treatment caused significant reduction in the HA titer, DTH responses, and antioxidant potential. In a triple antigen-mediated immunological edema model, the extent of edema raised in drug-treated rats was greater compared to that in control rats, thus confirming enhanced DTH reactions in response to the drug treatment. Based on the above findings, the reported immunomodulatory activity of an active fraction of O. indicum might be attributed to its ability to enhance specific immune responses (both humoral and cell-mediated) as well as its antioxidant potential.
Background Rheumatoid arthritis is the most common cause of disability, affecting 0.3–1% of the adult population worldwide. The latex of Calotropis procera possesses potent anti-inflammatory as well as analgesic properties. In light above facts, the present study was designed to evaluate anti-arthritic activity of Calotropis procera latex in complete Freund's adjuvant (CFA)-induced arthritis in Wistar albino rats. Complete Freund's adjuvant was injected into the left hind paw on day 0, and treatment of prednisolone and Calotropis procera latex was given from day 0 to 28. Various biochemical, hematological and functional parameters as well as radiological and histopathological changes of joint along with body weight and paw volume were measured. Results Calotropis procera treatment significantly lowered paw volume in CFA-induced arthritic rats. Significant improvement was observed in functional, biochemical and hematological parameters in Calotropis procera-treated rats. However, the body weight remained unaffected. Histological and radiographical examination of synovial joints in Calotropis procera-treated animals exhibited less synovial hyperplasia, infiltration and accumulation of inflammatory cell in synovial fluid, cartilage and bone erosion and joint space narrowing. Conclusion Calotropis procera latex possesses anti-arthritic activity, which is facilitated by modulation in the level of inflammatory mediators and oxidative stress. The improvement in hematological as well as biochemical parameters might be reflected on functional, histopathological, radiological changes and thereby disease progression.
The present study evaluated the immunomodulatory activity and mechanism of action of the n-butanol extract [100 mg/kg body weight (b.w.), per oral (p.o.)] of Oroxylum indicum Vent. (Bignoniaceae) root bark against different experimental animal models, i.e., immune response to sheep red blood cells in stress-induced immunosuppression, carbon clearance assay and neutrophil adhesion test. In the immune response to sheep red blood cell model, the n-butanol extract of Oroxylum indicum treatment group showed a significant rise (P < 0.05) in circulating antibody-titer as compared to the stress-induced control group. This observation suggests that the drug treatment caused potentiation of humoral antibody immune response to antigen. Also, it significantly decreases the rise in malondialdehyde content along with an increase (p < 0.05) in superoxide dismutase, catalase and reduced glutathione levels as compared to the stress-induced control group and, thus, exhibits significant antioxidant potential. Pretreatment with the n-butanol extract of Oroxylum indicum showed a significant rise (P < 0.05) in phagocytic index indicating phagocytic activity. In the neutrophil adhesion model, a significant increase (P < 0.05) in percentage neutrophil adhesion was observed in the n-butanol extract treatment group as compared to the control group. From these findings, the n-butanol extract of Oroxylum indicum possesses immunomodulatory activity by enhancing specific immune response (humoral immunity) and non-specific immune response (phagocytosis) of the body as well as exhibiting antioxidant potential. Our results suggest that the n-butanol extract of Oroxylum indicum root bark possesses a significant immunostimulant activity.
SUMMARYBlack pepper (family Piperaceae), is called king of spices because it is one of the oldest spice and alone accounts for about 35% of the world's total spice trade. The pepper is used in Ayurvedic medicine for the treatment of various ailments particularly neurological, broncho-pulmonary and gastrointestinal disorders. Pepper has also been reported to have various pharmacological actions but recently, it is highlighted as a bioavailability enhancer. This results in higher plasma concentration of drugs, nutrients, ions and other xenobiotics, rendering them more bioavailable for physiological as well as pharmacological actions in the body. Numerous scientific studies reported that piperine; a main bioactive compound of pepper, is responsible for its bioavailability enhancing property. It's a well known fact that pepper enhances bioavailability by inhibition of microsomal enzyme system but other mechanisms are also responsible to acts as a bioavailability enhancer. The brief overview of the mechanism of action of pepper as well as its applications as bioavailability enhancer is given in the present article.
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