1998
DOI: 10.1111/j.1527-3466.1998.tb00341.x
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Tetrandrine

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Cited by 26 publications
(27 citation statements)
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References 36 publications
(20 reference statements)
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“…It is believed that proliferation of fibroblasts plays an important role in hypertrophic scar formation and is involved in reepithelialization, extracellular matrix (ECM) deposition, neovascularization, and ECM remodeling (van der Veer et al, 2009). Both experimental and clinical researchers have shown that tetrandrine, a bisbenzylisoquinoline alkaloid isolated from the root of Stephania tetrandra, exerted antiinflammatory properties, attenuated ECM deposition, and exhibited antifibrogenic activity against fibroblasts (Reist et al, 1993;Huang and Hong, 1998;Oh and Lee, 2003). Our previous studies have provided evidence that tetrandrine significantly inhibits proliferation of hypertrophic scar fibroblasts (HSFs) and decreases the expression of DNA (Liu et al, 2001).…”
Section: Introductionmentioning
confidence: 99%
“…It is believed that proliferation of fibroblasts plays an important role in hypertrophic scar formation and is involved in reepithelialization, extracellular matrix (ECM) deposition, neovascularization, and ECM remodeling (van der Veer et al, 2009). Both experimental and clinical researchers have shown that tetrandrine, a bisbenzylisoquinoline alkaloid isolated from the root of Stephania tetrandra, exerted antiinflammatory properties, attenuated ECM deposition, and exhibited antifibrogenic activity against fibroblasts (Reist et al, 1993;Huang and Hong, 1998;Oh and Lee, 2003). Our previous studies have provided evidence that tetrandrine significantly inhibits proliferation of hypertrophic scar fibroblasts (HSFs) and decreases the expression of DNA (Liu et al, 2001).…”
Section: Introductionmentioning
confidence: 99%
“…The main ingredients in this herb are tetrandrine and fangchinoline (Sutter & Wang 1993). Tetrandrine works as a calcium entry blocker (Felix et al 1992), showing various actions, such as the modulation of cardiovascular disorders (Huang & Hong 1998), and anti-tumour (Lee et al 2002) and anti-inflammatory effects (Shen et al 1999). Fangchinoline is thought to be less potent than tetrandrine as a vasodilator or calcium channel blocker (Kim et al 1997).…”
Section: Introductionmentioning
confidence: 99%
“…The introduction of structurally new compounds as alternatives to existing antimicrobial agents enables the diversification of medicine and extends the shelf-life of available drugs and therapies, thereby delaying the MDR problem. TET has long generated considerable interest, mainly due to its cardiovascular electrophysiological properties as a Ca 2+ antagonist (Fang and Jiang, 1986;Sutter and Wang, 1993;Huang and Hong, 1998;Yao and Jiang, 2002). Therefore, it was considered that TET, which is a plant-based efflux pump inhibitor, might be a good candidate for clinical use as a resistance-modifying agent.…”
Section: Discussionmentioning
confidence: 99%