Whitt D D, Savage D C
Infect Immun. 1980 Jul;29(1):144-51. doi: 10.1128/iai.29.1.144-151.1980.
The concentration of protein and the activities of alkaline phosphatase, maltase, and sucrase were measured in saline extracts of the proximal small intestine of germfree and ex-germfree mice colonized with an indigenous microflora. The two populations of animals were maintained in plastic film isolators under tightly controlled environmental and nutritional conditions. Samples were taken at 0, 4, 8, 12, and 17 days and at 3, 4, 5, 6, 7, and 8 weeks after association. The activities were expressed as specific activities and as total units per segment of small intestine. Enzymatic activities expressed in both ways fluctuated considerably in the samples taken from one time to the next in animals of both types. The activities expressed as total units per segment of bowel of all three enzymes had decreased from levels in germfree animals by as early as 4 days after association. The total units of activity per segment of bowel tested continued to decrease for approximately 3 weeks in the associated animals to levels two- to fivefold lower than those of germfree animals. However, the specific activities of the three enzymes in the animals of the two types became less disparate at later sample times. This latter result is predictable because the concentration of protein extractable from the small intestines of the mice of the two types was the same at the beginning of the experiment, but by the later sampling times, the concentration of protein extractable from small bowels of ex-germfree mice was significantly lower than that from germfree mice. The fluctuations in levels of the enzymatic activities, even under controlled environmental and nutritional conditions, point to the necessity of using such conditions and a kinetic approach in studies of the effects of the microbiota on the activities of enzymes in the microvillous membranes of small bowel enterocytes. The changes in protein concentrations suggest that such activities and the amounts of protein extractable from the mucosa are influenced by different properties of the microflora. Thus, studies in which the enzymes are extracted from the entire mucosa and the activities are expressed as units per weight of extractable protein may give misleading results concerning the influence of the microbiota on the enterocyte membranes.
对定殖有本土微生物群的无菌小鼠和无菌后小鼠近端小肠的盐提取物中的蛋白质浓度以及碱性磷酸酶、麦芽糖酶和蔗糖酶的活性进行了测量。这两组动物饲养在塑料薄膜隔离器中,环境和营养条件受到严格控制。在定殖后的0、4、8、12和17天以及3、4、5、6、7和8周采集样本。酶活性以比活性和每段小肠的总单位数表示。在两种类型动物中,从一次采集到下一次采集的样本中,以这两种方式表示的酶活性都有相当大的波动。早在定殖后4天,所有三种酶以每段肠的总单位数表示的活性就已从无菌动物的水平下降。在定殖动物中,每段肠测试的活性总单位数在大约3周内持续下降,降至比无菌动物低两到五倍的水平。然而,在后期采样时,两种类型动物中三种酶的比活性差异变小。后一个结果是可以预测的,因为在实验开始时,从两种类型小鼠的小肠中可提取的蛋白质浓度相同,但到后期采样时,无菌后小鼠小肠中可提取的蛋白质浓度明显低于无菌小鼠。即使在受控的环境和营养条件下,酶活性水平的波动也表明,在研究微生物群对小肠肠上皮细胞微绒毛膜中酶活性的影响时,使用这些条件和动力学方法是必要的。蛋白质浓度的变化表明,这种活性和从粘膜中可提取的蛋白质数量受微生物群不同特性的影响。因此,从整个粘膜中提取酶并将活性表示为每重量可提取蛋白质的单位数的研究,可能会在微生物群对肠上皮细胞膜的影响方面给出误导性结果。