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用丸剂形式的外源性β-D-半乳糖苷酶治疗乳糖不耐受症。

Treatment of lactose intolerance with exogenous beta-D-galactosidase in pellet form.

作者信息

Xenos K, Kyroudis S, Anagnostidis A, Papastathopoulos P

机构信息

Department of Dermatology, University of Athens, A. Sygros Hospital, Greece.

出版信息

Eur J Drug Metab Pharmacokinet. 1998 Apr-Jun;23(2):350-5. doi: 10.1007/BF03189363.

Abstract

The effectiveness of a new beta-D-galactosidase pellet formulation in the treatment of lactose intolerance was studied. The encapsuled beta-D-galactosidase (lactase) pellets were first tested in vitro for their enzymatic activity within an environment simulating gastric conditions and subsequently within an environment simulating duodenal conditions. Effectiveness was measured by the % of glucose formed by hydrolysis of lactose. The pellets were found to retain their enzymatic activity in gastric pH conditions (mean 69 +/- 1 mg/dl glucose) and were found to hydrolyse lactose in human duodenal fluid (106.35 +/- 1 mg/dl). Finally the effectiveness of the new lactase formulation on glucose absorption was studied in 8 lactose intolerant subjects in a randomized, double blind, crossover trial. After fasting, the subjects were given one capsule containing 100 u/ml beta-galactosidase (i.e. 10 pellets of 10 u/ml each) or one capsule containing placebo pellets, followed by 100 g lactose dissolved in water. The washout period between lactose challenges was one week. Plasma glucose concentrations were measured before and at intervals after the challenges and the subjects completed symptom questionnaires every eight hours for 24 hours. Results showed a statistically significant increase in plasma glucose levels 30, 60, 90 and 120 min after lactose ingestion (repeated measures analysis of variance, p<0.01). Subjective ratings of the severity of abdominal cramping, belching, flatulence, vomiting and diarrhoea were significantly decreased following ingestion of the lactase pellets and lactose (no incidence of diarrhoea) compared with after ingestion of placebo and lactose. The results of the study were considered to be very promising as the beta-D-galactosidase formulation (which was produced at very low cost and with great ease) resisted inactivation in the stomach, effectively transformed lactose to glucose in vivo and reduced symptoms of lactose intolerance.

摘要

研究了一种新型β-D-半乳糖苷酶微丸制剂治疗乳糖不耐受的有效性。将包封的β-D-半乳糖苷酶(乳糖酶)微丸首先在模拟胃部条件的环境中进行体外酶活性测试,随后在模拟十二指肠条件的环境中进行测试。通过乳糖水解产生的葡萄糖百分比来衡量有效性。发现这些微丸在胃部pH条件下保留其酶活性(平均69±1mg/dl葡萄糖),并且发现在人十二指肠液中能水解乳糖(106.35±1mg/dl)。最后,在一项随机、双盲、交叉试验中,对8名乳糖不耐受受试者研究了这种新型乳糖酶制剂对葡萄糖吸收的有效性。禁食后,给受试者服用一粒含有100u/mlβ-半乳糖苷酶的胶囊(即10粒每粒10u/ml的微丸)或一粒含有安慰剂微丸的胶囊,随后饮用溶解在水中的100g乳糖。两次乳糖激发试验之间的洗脱期为一周。在激发试验前和激发试验后的不同时间间隔测量血浆葡萄糖浓度,并且受试者每8小时填写一次症状问卷,共24小时。结果显示,乳糖摄入后30、60、90和120分钟,血浆葡萄糖水平有统计学意义的显著升高(重复测量方差分析,p<0.01)。与服用安慰剂和乳糖后相比,服用乳糖酶微丸和乳糖后(无腹泻发生),腹部绞痛、嗳气、肠胃胀气、呕吐和腹泻严重程度的主观评分显著降低。该研究结果被认为非常有前景,因为这种β-D-半乳糖苷酶制剂(生产成本非常低且易于生产)在胃中能抵抗失活,在体内能有效地将乳糖转化为葡萄糖,并减轻乳糖不耐受症状。

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