INT129960
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Ciprofloxacin, norfloxacin and ofloxacin each reduced both basal and stimulated expression of MMP-13 mRNA. | |||||||||||||||
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Given that HDAC activity is typically associated with transcriptional repression [47], this result is consistent with the decrease in MMP-1 and MMP-13 gene expression in cells treated with a combination of both ligands, suggesting that the compounds may be inhibiting expression of these genes through a common histone acetylation-associated mechanism. | |||||||||||||||
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Figure 3 shows a decrease in expression of MMP-1 and MMP-13 at the transcriptional level in cells treated with LG268 and rosiglitazone. | |||||||||||||||
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ligand rosiglitazone suppresses MMP-1 and MMP13 gene expression more effectively than either compound alone. | |||||||||||||||
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As a result, combined treatment should lead to greater inhibition of MMP-1 and MMP-13 gene expression compared with either compound alone. | |||||||||||||||
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, ligands block MMP-1 and MMP-13 gene expression, RXR:PPAR? | |||||||||||||||
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, and MMP13 gene expression decreased. | |||||||||||||||
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Pretreatment with 2.5 and 10 mmol/l glucosamine was able, to differing degrees, to downregulate mRNA and protein levels of MMP-1, MMP-3 and MMP-13. | |||||||||||||||
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Interestingly, the most potent inhibitor of MMP-1 and MMP-13 production was LY83583, an inhibitor of NO-dependent soluble guanylate cyclase and of cGMP. | |||||||||||||||
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In the present study, subtle differences are shown in the pattern of inhibition of the ET-1-induced overproduction of MMP-1 and MMP-13. | |||||||||||||||
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Treatment group MMP-13 gene expression decreased to 0.55 (p = 0.19), and TNF? | |||||||||||||||
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To elucidate whether MMP-1, MMP-8 and MMP-13 levels in blood were high in patients with unstable angina (UAP), we measured serum MMP-1 and plasma MMP-8 and MMP-13 levels in 45 patients with UAP, 175 with stable coronary artery disease (CAD), and 45 controls. | |||||||||||||||
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The group of patients receiving 1 mg of sCT exhibited significant decreases in the levels of CTX-II, C2C, and MMP-13. | |||||||||||||||
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In comparison with controls, OA explants from five patients cultured in the presence of 10 pg/ml PGE2 showed decreased expression of the genes related to chondrocyte hypertrophy, namely those encoding COL10A1 and MMP-13 (Figure 3). | |||||||||||||||
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In the same line of thought, a study performed by Legendre and colleagues [32] recently demonstrated a similar inhibitory effect of rhein on MMP-13 production in articular chondrocytes. | |||||||||||||||
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Our results showed that EGCG pretreatment of cultured human OA chondrocytes significantly inhibited the expression and activities of MMP-1 and MMP-13 in a dose-dependent manner [21]. | |||||||||||||||
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These findings are in accordance with a study conducted in the dog ACL model in which Licofelone, a dual inhibitor of 5-lipoxygenase and COX activity, inhibited the development of cartilage lesions and subchondral bone resorption by reducing the synthesis of MMP-13 and cathepsin K, as well as other enzymes and growth factors that are involved in bone remodelling [93]. | |||||||||||||||
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The PPS salts are also potent inhibitors of granulocyte elastase and the serine proteinases of the complement and fibrinolytic systems, as well as downregulating MMP-13 production at the gene promotor level ([18-21] and references cited within). | |||||||||||||||
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It was recently reported that phenyl N-tert-butylnitrone, a spin-trap agent, downregulates IL-1-induced MMP-13 expression via the inhibition of the c-Jun amino-terminal kinase pathway in OA chondrocytes [61]. | |||||||||||||||
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Recent studies have revealed that pretreatment of human OA chondrocytes with EGCG significantly, in a dose-dependent manner, inhibited the expression and activities of MMP-1 and MMP-13 (IC50 values 27 and 16.5 ? | |||||||||||||||
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