Sugai N, Ninomiya Y, Oosaki T
Histochemistry. 1981;72(3):415-24. doi: 10.1007/BF00501783.
The localization of carbonic anhydrase in the rat lung has been demonstrated, at light and electron microscopic levels, by the cobalt bicarbonate histochemical method of Hansson. Focal deposits of the cobalt sulfide reaction product were found not only in the capillary endothelium of the alveolar walls, but also in the small and large alveolar cells. The histochemical reaction was abolished by two potent inhibitors, acetazolamide (10(-5) to 10(-6) M) and KCNO (5 x 10(-3) to 10 x 10(-3) M). Physiological assay with Maren's method indicated that values for carbonic anhydrase activity in rat lung are 4.4 +/- 0.8 UA/mg of protein, 25.0 +/- 5.5 UA/mg of nitrogen, and 369 +/- 86 UA/g of wet weight. In addition, it was calculated that after fixation in glutaraldehyde-formaldehyde-picric acid about 9% activity is retained.
通过汉森的碳酸氢钴组织化学方法,在光学和电子显微镜水平上证实了碳酸酐酶在大鼠肺中的定位。不仅在肺泡壁的毛细血管内皮中发现了硫化钴反应产物的局灶性沉积,在小肺泡细胞和大肺泡细胞中也有发现。两种强效抑制剂乙酰唑胺(10^(-5)至10^(-6)M)和氰酸钾(5×10^(-3)至10×10^(-3)M)可消除组织化学反应。采用马伦方法进行的生理学测定表明,大鼠肺中碳酸酐酶活性的值为每毫克蛋白质4.4±0.8UA、每毫克氮25.0±5.5UA以及每克湿重369±86UA。此外,经计算,在戊二醛 - 甲醛 - 苦味酸固定后,约保留9%的活性。