To evaluate the chondroprotective effect of L-carnitine in relation to glucosamine sulfate and in an experimental model of osteoarthritis (OA). Materials and methods: Thirty-two adult male Wister albino rats weighing 150-210 g were assigned randomly into 4 groups: 8 rats in each group, group I (control group), group II (MIA induced OA group), group III (MIA induced OA + glucosamine sulfate treated group), and group IV (MIA induced OA + L-carnitine treated group). Weight, knee diameter, and knee bend score were recorded on days 0, 1, 7, 14 and 28. On day 28 all animals were sacrificed. Synovial fluid of left knee was collected, and the interleukin-1b (IL-1b), Cartilage oligomeric matrix protein (COMP) and matrix metalloproteinase-13 (MMP-13) levels were measured by ELISA. The knee joints were removed and stained with H&E for histological evaluation. Results: The pathological abnormalities attributed to MIA induced arthritis was dramatically lowered in rats treated with glucosamine or L-carnitine. Synovial fluid levels of IL-1b, COMP and MMP-13 were increased in OA group, and significantly reduced with glucosamine or L-carnitine treated groups. Conclusion: L-Carnitine has a potential chondroprotective effect in this animal model of OA.
Background:
Boswellia serrata (family Burseraceae) has been traditionally used for the
treatment of a wide variety of diseases as arthritis, inflammatory bowel diseases, and airway diseases.
However, the direct bronchodilator efficacy of Boswellia serrata hasn’t been explored yet.
Objective:
We aimed at the present study to evaluate the direct effect of Boswellia serrata extract
(BSE) on isolated rat tracheal preparations precontracted with either Acetylcholine (ACh) or potassium
chloride (KCl).
Methods:
Tracheal rings were prepared from male Wistar rats (200-250 g). BSE (1-200 μg/ml) was
added to tracheal strips precontracted with either ACh or KCl and the response was observed. We
also investigated the consequences of epithelial denudation, indomethacin, and N-Nitro-L-arginine
on the relaxant effect of BSE as compared to that of the β-adrenoceptor agonist isoprenaline, or the
bitter taste receptor (TAS2R) agonist denatonium benzoate. Finally, the possible additive effects of
BSE to isoprenaline or denatonium-induced relaxation were evaluated.
Results:
By using a set of serial dosing and washout experiments with tracheal rings, results showed
that exposure to BSE resulted into a significant and concentration-dependent inhibitory effect on
airway smooth muscle contractions precontracted with either ACh or KCl. Epithelial denudation, indomethacin,
or N-Nitro-L-arginine had no significant effect on the obtained relaxation. Furthermore,
BSE potentiated the relaxant effect of isoprenaline on rat trachea.
Conclusion:
BSE exerts a direct concentration-dependent relaxant effect on precontracted tracheal
strips. These results could contribute towards validation of the traditional use of BSE in the treatment
of airway diseases.
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