Seow F, Katelaris P, Ngu M
Gastroenterology Unit, Repatriation General Hospital, Concord, Sydney, Australia.
Parasitology. 1993 Apr;106 ( Pt 3):233-8. doi: 10.1017/s0031182000075053.
Giardia lamblia localize and multiply in the small intestine and may cause acute or chronic diarrhoea with malabsorption of fat, protein and other nutrients. Abnormal pancreatic function has been documented in giardiasis and trophozoites directly inhibit pancreatic lipase activity in vitro. The aim of this study was to examine the effect of Giardia trophozoites on pancreatic trypsin, chymotrypsin and amylase activity in vitro. Axenically cultured Giardia trophozoites (Portland-1 stock) were incubated with a range of concentrations of trypsin, chymotrypsin and amylase and enzyme activity assayed over time. Tryptic activity was decreased after incubation with Giardia trophozoites. This reduction was time dependent and linear over the incubation period of 2 h. At a trypsin concentration of 18 BAEE units/ml, there was a 35.5 +/- 4% reduction in enzyme activity after 2 h compared to controls. The total amount of activity lost was proportional to the initial trypsin concentration up to 185 BAEE units/ml. At this initial concentration, the activity was reduced by 46.5 +/- 3 units/ml after 2 h. Above this concentration, little further loss of enzyme activity was seen. To investigate the nature and specificity of this effect, similar experiments were conducted using killed trophozoites and with a related protozoan, Trichomonas vaginalis. No loss of enzyme activity was evident. Media previously incubated for 2 h with trophozoites did not diminish tryptic activity. Trophozoites had no effect on chymotrypsin or amylase activities over the range of concentrations tested.(ABSTRACT TRUNCATED AT 250 WORDS)
蓝氏贾第鞭毛虫定位于小肠并在其中繁殖,可导致急性或慢性腹泻,并伴有脂肪、蛋白质和其他营养物质的吸收不良。贾第虫病患者已被证明存在胰腺功能异常,且滋养体在体外可直接抑制胰腺脂肪酶活性。本研究的目的是检测贾第虫滋养体在体外对胰腺胰蛋白酶、糜蛋白酶和淀粉酶活性的影响。将无菌培养的贾第虫滋养体(波特兰-1株)与一系列浓度的胰蛋白酶、糜蛋白酶和淀粉酶一起孵育,并随时间测定酶活性。与贾第虫滋养体孵育后,胰蛋白酶活性降低。这种降低是时间依赖性的,在2小时的孵育期内呈线性关系。在胰蛋白酶浓度为18 BAEE单位/毫升时,与对照组相比,2小时后酶活性降低了35.5±4%。直至185 BAEE单位/毫升,活性丧失的总量与初始胰蛋白酶浓度成正比。在此初始浓度下,2小时后活性降低了46.5±3单位/毫升。高于此浓度,未见酶活性进一步丧失。为研究这种作用的性质和特异性,使用灭活的滋养体以及相关原生动物阴道毛滴虫进行了类似实验。未发现酶活性有明显丧失。先前与滋养体孵育2小时的培养基并未降低胰蛋白酶活性。在所测试的浓度范围内,滋养体对糜蛋白酶或淀粉酶活性没有影响。(摘要截短至250字)