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采用酶免疫测定法测定兔肾单位中前列腺素E2的合成。

Determination of prostaglandin E2 synthesis along rabbit nephron by enzyme immunoassay.

作者信息

Farman N, Pradelles P, Bonvalet J P

出版信息

Am J Physiol. 1986 Aug;251(2 Pt 2):F238-44. doi: 10.1152/ajprenal.1986.251.2.F238.

Abstract

Prostaglandin E2 (PGE2) content and synthesis have been measured in microdissected segments from the entire nephron of rabbit kidney. PGE2 was determined by an enzyme immunoassay on glomeruli or tubular segments (0.5-5 mm) either immediately after microdissection (PGE2 content) or after incubation for 15 min at 37 degrees C in the presence of arachidonic acid (PGE2 synthesis). We confirmed that collagenase used for microdissection did not modify PGE2 synthesis. A linear correlation was found between the length of tubule used in the assay and PGE2 synthesis, as well as between incubation time with arachidonic acid and PGE2 synthesis. PGE2 synthesis, expressed in picograms per millimeter tubular length per 15 min, was maximum in medullary collecting duct (517 +/- 73). High values were also found in the granular portion of distal tubule (134 +/- 22) and granular or light portion of cortical collecting tubule (199 +/- 24 and 146 +/- 10, respectively). Synthesis was lower in all other segments: 17 +/- 6 and 24 +/- 12, respectively, in convoluted and straight proximal tubule, 67 +/- 12 and 71 +/- 5, respectively, in thin descending and ascending limb, 51 +/- 9 and 23 +/- 4, respectively, in medullary and cortical thick ascending limb of Henle's loop, and 25 +/- 7 in initial distal tubule. Synthesis per glomerulus was 24 +/- 3. When the protein content of each nephron segment is taken into account, this profile was not modified, except for the thin limbs of the loop, which reached values per nanogram protein slightly higher than those of the cortical collecting tubule.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已对兔肾全肾单位经显微切割的节段中的前列腺素E2(PGE2)含量及合成进行了测定。PGE2通过酶免疫测定法来确定,测定对象为显微切割后即刻的肾小球或肾小管节段(0.5 - 5毫米)(PGE2含量),或在37℃下于花生四烯酸存在的条件下孵育15分钟后的样本(PGE2合成)。我们证实,用于显微切割的胶原酶不会改变PGE2的合成。在测定中使用的肾小管长度与PGE2合成之间,以及与花生四烯酸的孵育时间和PGE2合成之间均发现存在线性相关性。以每15分钟每毫米肾小管长度的皮克数表示的PGE2合成,在髓质集合管中最高(517±73)。在远曲小管的颗粒部(134±22)以及皮质集合小管的颗粒部或淡染部(分别为199±24和146±10)也发现有较高值。在所有其他节段中合成较低:在近曲小管的曲部和直部中分别为17±6和24±12,在细段降支和升支中分别为67±12和71±5,在亨氏袢的髓质和皮质厚升支中分别为51±9和23±4,在远曲小管起始段中为25±7。每个肾小球的合成量为24±3。当考虑每个肾单位节段的蛋白质含量时,除了袢的细段外,这种分布情况未发生改变,细段每纳克蛋白质的合成量略高于皮质集合小管。(摘要截短于250字)

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