University of California San Diego, La Jolla, CA 92093-0956, USA.
Am J Gastroenterol. 2013 Jan;108(1):90-8. doi: 10.1038/ajg.2012.340. Epub 2012 Oct 9.
Andrographis paniculata has in vitro inhibitory activity against TNF-α, IL-1β and NF-κB. A pilot study of A. paniculata extract (HMPL-004) suggested similar efficacy to mesalamine for ulcerative colitis.
A randomized, double-blind, placebo-controlled trial evaluated the efficacy of A. paniculata extract (HMPL-004) in 224 adults with mild-to-moderate ulcerative colitis. Patients were randomized to A. paniculata extract (HMPL-004) 1,200 mg or 1,800 mg daily or placebo for 8 weeks.
In total, 45 and 60% of patients receiving A. paniculata 1,200 mg and 1,800 mg daily, respectively, were in clinical response at week 8, compared with 40% of those who received placebo (P=0.5924 for 1,200 mg vs. placebo and P=0.0183 for 1,800 mg vs. placebo). In all, 34 and 38% of patients receiving A. paniculata 1,200 mg and 1,800 mg daily, respectively, were in clinical remission at week 8, compared with 25% of those who received placebo (P=0.2582 for 1,200 mg vs. placebo and P=0.1011 for 1,800 mg vs. placebo). Adverse events developed in 60 and 53% of patients in the A. paniculata 1,200 mg and 1,800 mg daily groups, respectively, and 60% in the placebo group.
Patients with mildly to moderately active ulcerative colitis treated with A. paniculata extract (HMPL-004) at a dose of 1,800 mg daily were more likely to achieve clinical response than those receiving placebo.
穿心莲在体外对 TNF-α、IL-1β 和 NF-κB 具有抑制活性。一项穿心莲提取物(HMPL-004)的初步研究表明,其对溃疡性结肠炎的疗效与美沙拉嗪相似。
一项随机、双盲、安慰剂对照试验评估了穿心莲提取物(HMPL-004)在 224 名轻中度溃疡性结肠炎成人患者中的疗效。患者被随机分为穿心莲提取物(HMPL-004)1200mg 或 1800mg 每日或安慰剂组,治疗 8 周。
接受穿心莲 1200mg 和 1800mg 每日治疗的患者分别有 45%和 60%在第 8 周达到临床缓解,而接受安慰剂的患者为 40%(1200mg 与安慰剂相比,P=0.5924;1800mg 与安慰剂相比,P=0.0183)。接受穿心莲 1200mg 和 1800mg 每日治疗的患者分别有 34%和 38%在第 8 周达到临床缓解,而接受安慰剂的患者为 25%(1200mg 与安慰剂相比,P=0.2582;1800mg 与安慰剂相比,P=0.1011)。接受穿心莲 1200mg 和 1800mg 每日治疗的患者分别有 60%和 53%出现不良事件,安慰剂组为 60%。
与接受安慰剂的患者相比,接受穿心莲提取物(HMPL-004)1800mg 每日治疗的轻度至中度活动期溃疡性结肠炎患者更有可能达到临床缓解。