Laverty Gary, Alberici Mary
University of Delaware, School of Life and Health Sciences, Newark, Delaware 19716.
J Morphol. 1991 Mar;207(3):273-281. doi: 10.1002/jmor.1052070305.
A histochemical investigation of kidney and lower intestine of the European starling (Sturnus vulgaris) shows no carbonic anhydrase activity in proximal convoluted tubules, although activity is seen in similarly prepared sections of rat proximal tubules. Early distal tubule cells in the starling are stained throughout the cytoplasm and at the apical and highly infolded basolateral membranes. Late distal tubules lose apical activity and have reduced basolateral infolding, resulting in less intense staining. Darkly stained intercalated cells appear in the connecting tubules and cortical collecting ducts. Both of these segments also show intense basolateral staining. Medullary cones of the starling are highly organized, with central zones containing unstained thin descending limbs of loops of Henle, surrounded by both medullary collecting ducts with only scattered cells staining for enzyme, and by thick ascending limb segments. The latter contain many uniformly stained cells intermingled with occasional unstained cells. Scattered cells of the starling colonic villi demonstrate intense apical brush border membrane staining as well as cytoplasmic staining. Cells lining the cloaca stain less intensely. A biochemical assay for carbonic anhydrase was used to quantify enzyme activity in these tissues. Starling kidney contained 1.96 ± 0.33 (mean ± SEM) enzyme units/mg protein, less than half the activity seen in rat kidney. Stripped colonic epithelium contained 0.66 ± 0.15 enzyme units/mg protein. These quantitative results correlate well with the interpretations derived from the histochemical observations. The lack of proximal tubule carbonic anhydrase activity suggests that the avian kidney relies more on distal nephron segments to achieve net acidification of the urine.
对欧洲椋鸟(Sturnus vulgaris)的肾脏和下肠道进行的组织化学研究表明,近端曲管中没有碳酸酐酶活性,尽管在大鼠近端小管的类似制备切片中可见活性。椋鸟早期远端小管细胞的整个细胞质以及顶端和高度内褶的基底外侧膜均被染色。晚期远端小管失去顶端活性,基底外侧内褶减少,导致染色强度降低。深色染色的闰细胞出现在连接小管和皮质集合管中。这两个节段也显示出强烈的基底外侧染色。椋鸟的髓质锥体高度有组织,中央区域包含未染色的亨氏袢细降支,周围是髓质集合管,只有散在的细胞对酶染色,以及厚升支段。后者包含许多均匀染色的细胞,偶尔夹杂着未染色的细胞散在分布。椋鸟结肠绒毛的散在细胞显示出强烈的顶端刷状缘膜染色以及细胞质染色。泄殖腔内衬细胞的染色强度较低。使用碳酸酐酶的生化测定法对这些组织中的酶活性进行定量。椋鸟肾脏含有1.96±0.33(平均值±标准误)酶单位/毫克蛋白质,不到大鼠肾脏中活性的一半。剥离的结肠上皮含有0 .66±0.15酶单位/毫克蛋白质。这些定量结果与从组织化学观察得出的解释密切相关。近端小管碳酸酐酶活性的缺乏表明,鸟类肾脏更多地依赖远端肾单位节段来实现尿液的净酸化。