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新型鱼油衍生物对一组克罗恩病患者脂肪酸磷脂膜模式的影响。

Effects of new fish oil derivative on fatty acid phospholipid-membrane pattern in a group of Crohn's disease patients.

作者信息

Belluzzi A, Brignola C, Campieri M, Camporesi E P, Gionchetti P, Rizzello F, Belloli C, De Simone G, Boschi S, Miglioli M

机构信息

Istituto di Clinica Medica e Gastroenterologia, Cattedra di Medicina, d'Urgenza, Servizio di Farmacologia Clinica, Bologna, Italy.

出版信息

Dig Dis Sci. 1994 Dec;39(12):2589-94. doi: 10.1007/BF02087694.

Abstract

Fish oil has been recently proposed as a possible effective treatment in inflammatory bowel disease (IBD); however, a lot of annoying side effects (ie, belching, halitosis, diarrhea, etc) affect patient compliance. We carried out a study of patient tolerance in a group of Crohn's disease (CD) patients with a new fish oil derivative consisting of 500-mg capsules of eicosapentaenoic-docosahexaenoic (EPA 40%-DHA 20%), a free fatty acid mixture (Purepa), and we also evaluated its incorporation into phospholipids, both in plasma and in red cell membranes. Five groups of 10 CD patients in remission received nine Purepa capsules daily in four different preparations (A: uncoated, B: coated, pH 5.5; C: coated, pH 5.5, 60 min time release; D: coated, pH 6.9) and 12 x 1-g capsules daily of a triglyceride preparation (Max-EPA, EPA 18%-DHA 10%), respectively. We coated three of the four Purepa preparations in order to delay the release of contents in an attempt to minimize the side effects. After six weeks of treatment, the group taking Purepa capsules, coated, pH 5.5, 60 min time release (group C) showed the best incorporation of EPA and DHA in red blood cell phospholipid membranes (EPA from 0.2 to 4.4%, DHA from 3.7 to 6.3%), and no side effects were registered, whereas in all other groups side effects were experienced in 50% or more of subjects. This new preparation will make it possible to treat patients for long periods.

摘要

最近有人提出鱼油可能是治疗炎症性肠病(IBD)的一种有效疗法;然而,许多令人讨厌的副作用(如嗳气、口臭、腹泻等)影响了患者的依从性。我们对一组克罗恩病(CD)患者使用一种新的鱼油衍生物(由500毫克二十碳五烯酸 - 二十二碳六烯酸(EPA 40% - DHA 20%)的胶囊、一种游离脂肪酸混合物(Purepa)组成)进行了患者耐受性研究,并且我们还评估了其在血浆和红细胞膜中掺入磷脂的情况。五组处于缓解期的10名CD患者分别每天接受九粒不同制剂的Purepa胶囊(A:未包衣;B:包衣,pH 5.5;C:包衣,pH 5.5,60分钟缓释;D:包衣,pH 6.9)以及每天12粒1克的甘油三酯制剂胶囊(Max - EPA,EPA 18% - DHA 10%)。我们对四种Purepa制剂中的三种进行了包衣,以延缓内容物的释放,试图将副作用降至最低。治疗六周后,服用包衣、pH 5.5、60分钟缓释的Purepa胶囊的组(C组)在红细胞磷脂膜中显示出EPA和DHA的最佳掺入情况(EPA从0.2%至4.4%,DHA从3.7%至6.3%),并且未记录到副作用,而在所有其他组中,50%或更多的受试者出现了副作用。这种新制剂将使长期治疗患者成为可能。

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