Zhukova N L, Gedymin L E, Golyshevskaia V I
Vopr Med Khim. 1986 Sep-Oct;32(5):80-4.
Two series of experiments were carried out using 66 guinea pigs infected with tuberculosis. In the first experiment generalized tuberculosis was stimulated by means of subcutaneous administration of Mycobacterium tuberculosis H37RV strain at a dose of 0.0001 mg. In the second experiment destructive form of tuberculosis was developed after intrapulmonary administration of the bacteria (1 mg) followed by VCG vaccination. In both experiments the animals were divided into groups with spontaneous form of the infection and the group of animals treated with rifamycin and isoniazid. Total protein, elastolytic activity, cathepsins B and D, free antitryptic activity were estimated in lung homogenates. Generalized and destructive forms of tuberculosis were shown to induce an increase in content of soluble protein as well as in cathepsin D, elastolytic and antitryptic activities in tissues. Destructive form of tuberculosis was characterized by more than 4-fold increase in elastolytic activity and by a distinct activation of cathepsin B. The antibacterial drugs used affected only slightly the biochemical patterns studied in lung tissue.
使用66只感染结核病的豚鼠进行了两组实验。在第一个实验中,通过皮下注射剂量为0.0001毫克的结核分枝杆菌H37RV菌株来激发全身性结核病。在第二个实验中,在肺内注射细菌(1毫克)然后进行卡介苗接种后,诱发了破坏性肺结核。在两个实验中,动物均被分为自发感染组以及用利福霉素和异烟肼治疗的动物组。对肺匀浆中的总蛋白、弹性蛋白酶活性、组织蛋白酶B和D、游离抗胰蛋白酶活性进行了评估。结果显示,全身性和破坏性肺结核均会导致组织中可溶性蛋白含量以及组织蛋白酶D、弹性蛋白酶和抗胰蛋白酶活性增加。破坏性肺结核的特征是弹性蛋白酶活性增加4倍以上,组织蛋白酶B明显激活。所用的抗菌药物对肺组织中研究的生化模式影响甚微。