2004
DOI: 10.1016/j.phymed.2004.02.003
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Downregulation of iNOS expression in rat mesangial cells by special extracts of Harpagophytum procumbens derives from harpagoside-dependent and independent effects

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Cited by 65 publications
(49 citation statements)
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“…Although no significant treatment effect was observed for stimulated Cys-LT levels, a biphasic decrease in basal Cys-LT was established with a 28% reduction after 4 h and a 58% reduction after 8 h. Pharmacokinetic investigations revealed that maximum levels of harpagoside were attained after 1.3 to 2.5 h and a correlation was determined between serum harpagoside levels and LT inhibition. The relevance of basal Kaszkin et al, 2004Huang et al, 2005Langmead et al, 2002BetancorFernandez et al, 2003Fiebich et al, 2001Schulze-Tanzil et al, 2004;Goldring and Goldring, 2004Moussard et al, 1992Loew et al, 2001 Results No analgesic effect as measured by prostaglandin synthetase activity Antiinflammatory effect through suppression of biosynthesis of cysteinyl-leukotrienes (Cys-LT; LTC 4 , LTD 4 and LTE 4 ) and TXB 2 Antiinflammatory effect by inhibition of TXB 2 by platelets Direct inhibitory effect on the COX-2 enzyme Analgesic effect due to significant reduction in expression of PGE 2 Concentration-dependent suppressions in nitrite release and iNOS expression Significant inhibition of COX-2 and iNOS Antioxidant abilities Antiinflammatory effect through inhibition of proinflammatory cytokines Eicosanoid production not altered via the COX or 5-LOX pathways in healthy individuals Effect on eicosanoid biosynthesis implied by biphasic decrease in basal Cys-LT in healthy men eicosanoid levels to active inflammatory conditions rather than those released following stimuli, could be questioned, however. As found in the animal studies discussed previously, the apparent discrepancies in results yielded from these eicosanoid investigations could more than likely be attributed to the fact that standardized extracts, with a universal harpagoside content, were not used in every case.…”
Section: Preclinical Research (In Vitro and Ex Vivo)mentioning
confidence: 99%
“…Although no significant treatment effect was observed for stimulated Cys-LT levels, a biphasic decrease in basal Cys-LT was established with a 28% reduction after 4 h and a 58% reduction after 8 h. Pharmacokinetic investigations revealed that maximum levels of harpagoside were attained after 1.3 to 2.5 h and a correlation was determined between serum harpagoside levels and LT inhibition. The relevance of basal Kaszkin et al, 2004Huang et al, 2005Langmead et al, 2002BetancorFernandez et al, 2003Fiebich et al, 2001Schulze-Tanzil et al, 2004;Goldring and Goldring, 2004Moussard et al, 1992Loew et al, 2001 Results No analgesic effect as measured by prostaglandin synthetase activity Antiinflammatory effect through suppression of biosynthesis of cysteinyl-leukotrienes (Cys-LT; LTC 4 , LTD 4 and LTE 4 ) and TXB 2 Antiinflammatory effect by inhibition of TXB 2 by platelets Direct inhibitory effect on the COX-2 enzyme Analgesic effect due to significant reduction in expression of PGE 2 Concentration-dependent suppressions in nitrite release and iNOS expression Significant inhibition of COX-2 and iNOS Antioxidant abilities Antiinflammatory effect through inhibition of proinflammatory cytokines Eicosanoid production not altered via the COX or 5-LOX pathways in healthy individuals Effect on eicosanoid biosynthesis implied by biphasic decrease in basal Cys-LT in healthy men eicosanoid levels to active inflammatory conditions rather than those released following stimuli, could be questioned, however. As found in the animal studies discussed previously, the apparent discrepancies in results yielded from these eicosanoid investigations could more than likely be attributed to the fact that standardized extracts, with a universal harpagoside content, were not used in every case.…”
Section: Preclinical Research (In Vitro and Ex Vivo)mentioning
confidence: 99%
“…Using the reverse transcriptionalpolymerase chain reaction, Jang et al (2003) found that an aqueous extract of Hp caused a significant dosedependent (100-1000 μg/mL) inhibition of LPS-induced iNOS expression in L929 murine cells. Similarly, Kaszkin et al (2004) demonstrated significant concentrationdependent (0.3-1 mg/mL) suppressions in nitrite release and iNOS expression from Hp-treated IL-1β-stimulated rat mesangial cells. It was further demonstrated that Hp treatment inhibited the translocation of NF-κB from the nucleus which most probably explains the suppression of iNOS and thus nitrite release.…”
Section: Discussionmentioning
confidence: 84%
“…Harpagoside inhibited in vitro the synthesis of various proinflammatory mediators via suppression of iNOS and COX-2 expression through inhibition of NF-kappa B activation [61], but showed no anti-inflammatory activity in one animal model of inflammation (carrageenan-induced paw edema) [55]. The scientists suggested that other phytochemicals than harpagoside may be contributors to the anti-inflammatory effect of HP [55,62].…”
Section: Harpagophytum Procumbens Fam Pedaliaceaementioning
confidence: 99%