Department of Biochemistry & Nutrition, Central Food Technological Research Institute (CSIR), Mysore, India.
Indian J Med Res. 2010 May;131:682-91.
BACKGROUND & OBJECTIVES: Curcumin, capsaicin and piperine--the bioactive compounds present in spices--turmeric (Curcuma longa), red pepper (Capsicum annuum) and black pepper (Piper nigrum) respectively, have a considerable portion of structural homology. Tissue distribution and elimination of these three structurally similar bioactive compounds was examined following their oral intake in rats.
Separate sets of animals (150-160 g) were orally administered the three spice principles at dosages of 30 mg (capsaicin), 170 mg (piperine) and 500 mg (curcumin) / kg body weight. The tissue concentrations of administered spice compounds were determined by HPLC.
Maximum distribution of 24.4 per cent of administered capsaicin was seen at 1 h, while no intact capsaicin was detectable after 4 days. Absorption of capsaicin was about 94 per cent and very rapid relative to other two compounds. A maximum of 10.8 per cent of administered piperine was seen in tissues at 6 h. Absorption of the administered piperine was about 96 per cent. Curcumin concentration was maximum in the intestine at 1 h; maximum in blood at 6 h and remained at significantly higher level even at 24 h. About 63.5 per cent of the curcumin dose was absorbed. Only a small portion of the administered dose of capsaicin (< 0.1%) and curcumin (0.173 %) was excreted in urine, whereas piperine was not detectable in urine. Enhanced bioavailability of curcumin was evidenced when the same was orally administered concomitant with piperine. Intestinal absorption of curcumin was relatively higher when administered concomitantly with piperine, and it stayed significantly longer in the body tissues. Intact curcumin was detected in brain at 24, 48 and 96 h with a maximum at 48 h.
Considerable difference exists in the bioavailability of the three test compounds. Curcumin could be traced in the brain following its administration. Bioavailability of curcumin can be improved by co-administration with piperine.
姜黄素、辣椒素和胡椒碱——分别存在于香料中的生物活性化合物,姜黄(姜黄)、红辣椒(辣椒)和黑胡椒(胡椒)——具有相当大的结构同源性。在大鼠口服摄入这三种结构相似的生物活性化合物后,研究了它们在组织中的分布和消除情况。
分别给 150-160 克的动物口服给予三种香料成分,剂量为 30 毫克(辣椒素)、170 毫克(胡椒碱)和 500 毫克(姜黄素)/公斤体重。通过 HPLC 测定给予的香料化合物的组织浓度。
给予的辣椒素在 1 小时时最大分布 24.4%,而 4 天后检测不到完整的辣椒素。辣椒素的吸收率约为 94%,相对其他两种化合物吸收速度非常快。给予的胡椒碱在 6 小时时在组织中达到最大值 10.8%。给予的胡椒碱吸收率约为 96%。姜黄素在 1 小时时在肠道中浓度最高;6 小时时在血液中达到最大值,即使在 24 小时时仍保持在显著较高的水平。约 63.5%的姜黄素剂量被吸收。给予的辣椒素(<0.1%)和姜黄素(0.173%)的剂量只有一小部分排泄在尿液中,而胡椒碱在尿液中无法检测到。当姜黄素与胡椒碱同时口服时,证明其生物利用度增强。当与胡椒碱同时给予时,姜黄素的肠道吸收相对较高,并且在体内组织中停留时间明显延长。给予后 24、48 和 96 小时在大脑中检测到完整的姜黄素,最大浓度在 48 小时。
三种测试化合物的生物利用度存在显著差异。给予后可在大脑中检测到姜黄素。姜黄素的生物利用度可以通过与胡椒碱共同给药来提高。