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1
Studies of Uranium Poisoning: II. The Solubility of Uranium Oxide in Artificial and Human Gastric Juice.铀中毒研究:II. 氧化铀在人工胃液和人胃液中的溶解度
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2
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3
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4
THE HISTOGENESIS OF CHRONIC URANIUM NEPHRITIS WITH ESPECIAL REFERENCE TO EPITHELIAL REGENERATION.慢性铀肾病的组织发生,特别论及上皮再生。
J Exp Med. 1915 May 1;21(5):425-50. doi: 10.1084/jem.21.5.425.

铀硝酸盐第二次皮下注射后狗肾脏的功能和病理反应。

THE FUNCTIONAL AND PATHOLOGICAL RESPONSE OF THE KIDNEY IN DOGS SUBJECTED TO A SECOND SUBCUTANEOUS INJECTION OF URANIUM NITRATE.

机构信息

Laboratory of Pharmacology of the University of North Carolina, Chapel Hill.

出版信息

J Exp Med. 1929 Feb 28;49(3):411-33. doi: 10.1084/jem.49.3.411.

DOI:10.1084/jem.49.3.411
PMID:19869554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2131560/
Abstract

The present study permits the following conclusions. 1. Uranium nitrate in the dog has a high degree of selective affinity as a nephrotoxic for the epithelium of the proximal convoluted tubules. The glomeruli participate in the injury and develop obliterative connective tissue changes as evidence of a preexisting acute injury followed by repair. 2. The repair to the degenerated tubular epithelium is accomplished by two processes. First, by a regeneration of convoluted tubule cells from such cells not too severely injured in this location. This type of regenerated epithelium has no resistance to uranium. Second, the regeneration may occur as an ingrowth of cells or as syncytial buds from cells in the terminal portion of the proximal convoluted tubule or from the upper end of the descending limb of Henle's loop. This type of regenerated epithelium which is entirely different cytologically from normal convoluted tubule epithelium is resistant to a second injury from uranium even when the amount of this nephrotoxic agent has been increased to double the amount of the initial injection. 3. The kidney does not develop a local tissue immunity or resistance to uranium in the sense that cells of the same type once injured by it acquire as a result of the injury a resistance. The resistance and apparent but not real immunity is due to another type of cell with resistance having been substituted for a cell with but little resistance. This fact may be looked upon as constituting part of a defense mechanism in the kidney and may in part explain the long duration of certain types of chronic nephritic processes. 4. The functional studies which have been made during the initial injury from uranium to the tubules and during the secondary injury in animals which have either shown a resistance or a lack of resistance, emphasize the importance of the tubular epithelium as a part of a secretory mechanism in urine formation. During periods when the proximal convoluted tubule epithelium is in a state of acute degeneration there is a disturbance in the acid-base equilibrium of the blood, a reduction in the elimination of phenolsulphonephthalein and a retention of urea nitrogen, non-protein nitrogen and creatinine. When this epithelium is regenerated by the formation of a tubular epithelium normal in character for this location of the tubule, regardless of structural changes in the glomeruli, the above evidence of renal dysfunction returns to the normal. If at such a period this type of regenerated epithelium be injured by a secondary injection of uranium a state of acute renal dysfunction is induced in an intensified form. In those animals in which the repair to the tubules was accomplished by the formation of an atypical type of epithelium in the convoluted tubules as well as by the formation of cells normal in histological appearance for this part of the tubule there was an improvement in the degree of depletion of the reserve alkali of the blood, in the elimination of phenolsulphonephthalein and in the retention of urea nitrogen, non-protein nitrogen and creatinine. Certain of these values did not reach the normal. In such a state of renal repair when a second injection of uranium was given the kidney was found to have developed a marked resistance to it. There was but slight evidence of a depression in renal function. Associated with this acquired functional resistance there was no evidence of injury to the atypical, flattened regenerated epithelium of the proximal convoluted tubules.

摘要

本研究得出以下结论。1. 硝酸铀对犬近端曲管上皮具有高度选择性亲和力,是一种肾毒性物质。肾小球参与损伤,并发展为闭塞性结缔组织变化,表明存在先前的急性损伤,随后进行修复。2. 退化的管状上皮的修复通过两种过程完成。首先,通过未在此位置严重受损的曲管细胞的再生来完成。这种类型的再生上皮对铀没有抵抗力。其次,再生可能是曲管细胞的向内生长,或者是来自近端曲管末端或亨勒氏环下降支上部的细胞的合胞体芽的再生。这种类型的再生上皮在细胞学上与正常曲管上皮完全不同,即使将这种肾毒性物质的量增加到初始注射量的两倍,它也对第二次铀损伤具有抵抗力。3. 肾脏不会产生针对铀的局部组织免疫或抗性,因为曾经受到其伤害的同一类型的细胞由于损伤而获得了抗性。这种抗性和明显但不是真正的免疫力是由于具有抗性的另一种类型的细胞取代了具有很少抗性的细胞。这一事实可以被视为构成肾脏防御机制的一部分,并在一定程度上解释了某些类型的慢性肾炎过程持续时间长的原因。4. 在铀对肾小管的初始损伤期间和在具有抗性或缺乏抗性的动物的二次损伤期间进行的功能研究强调了管状上皮作为尿液形成中分泌机制的一部分的重要性。当近端曲管上皮处于急性退化状态时,血液的酸碱平衡会受到干扰,酚磺酞排泄减少,尿素氮、非蛋白氮和肌酐潴留。当这种上皮通过形成特征正常的管状上皮来再生时,无论肾小球的结构变化如何,上述肾功能障碍的证据都会恢复正常。如果在此期间,这种类型的再生上皮再次受到铀的二次注射损伤,会导致急性肾功能障碍加剧。在那些修复肾小管的动物中,通过形成典型的曲管上皮以及形成组织学上正常的管状上皮来完成修复,血液中储备碱的消耗程度、酚磺酞排泄和尿素氮、非蛋白氮和肌酐的潴留都会得到改善。某些值仍未达到正常水平。在这种肾脏修复状态下,再次给予铀注射时,肾脏对其产生了明显的抗性。肾功能下降的迹象很轻微。与这种获得的功能抗性相关的是,近端曲管上皮的典型扁平再生上皮没有受到损伤。