Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0033687 (proteinuria)
 24,015 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Pregnancy induced hypertension (PIH) in patient of essential hypertension is a high risk factor for both mother and child. From July 1959 to June 1991 there were 52,898 deliveries after the 28th week of gestation in our hospital, among whom essential hypertension occurred in 2.5% and 337 cases were superimposed by PIH with an incidence of 25.9%. There was a perinatal fetal mortality rate of 117.6/1000 in those 337 cases. A scoring system for perinatal fetal prognosis was worked out. The clinical criteria consist of: preexisting diastolic blood pressure, the highest diastolic pressure during pregnancy, proteinuria and the time of onset of PIH. A perinatal survival rate of 75.0% was obtained in those patients with preexisting diastolic pressure lower than 14.8 kPa (110 mmHg). A perinatal survival rate of more than 98.0% may be expected of those patients developing P I H after the 36th week of gestation. When the score is more than 8, the patient could usually get a living baby. If the score is less than 7, it is important to treat P I H effectively, terminate pregnancy at an appropriate time and keep the baby in the intensive care unit.
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PMID:[Perinatal fetal prognosis of essential hypertension complicating pregnancy]. 139

The immune nephritis antibody response against the collagen and glycoprotein portions of the glomerular basement membrane (GBM) has been monitored by using either type IV collagen prepared from pepsin digests or a collagenase digest of GBM. Sheep immunized with GBM, according to Steblay, respond by developing antibodies directed against the collagen and the glycoprotein portions, respectively. Circulating antibodies directed against sheep GBM structures were not demonstrated until overt clinical disease with high serum creatinine values and proteinuria. Such antibodies could, however, be eluted from the kidneys, where they adsorbed in a linear fashion as demonstrated by immunofluorescence microscopy. In spontaneous human nephritis in Goodpasture's syndrome, circulating antibodies were present at the time of diagnosis. These antibodies reacted only with the glycoprotein portion of the basement membrane, and not with the type IV collagen.
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PMID:Different antibody response in experimental and spontaneous glomerulonephritis. 732 28

In a previous in situ hybridization study, we demonstrated the mRNA expression of napsin, an aspartic protease of the pepsin family, in the kidney, lung, and lymphoid organs of mice. However, findings on the cellular localization of napsin at the protein level are controversial, and no information on the subcellular localization is available. The present immunohistochemical study revealed the cellular and subcellular localization of napsin in mice and rats, and also analyzed the influences of chemical-induced proteinuria on the renal expression of this enzyme in rats. Immunohistochemistry using a polyclonal antibody against mouse napsin showed that napsin immunoreactivity was noticeable in lysosomes of renal proximal tubule cells and in lamellar bodies of pulmonary type II alveolar cells. In the lung, immunoreactivity was also found in lysosomes of alveolar macrophages and on the surface of type I alveolar cells; the immunoreactivities in these cells may be due to the uptake and adhesion of napsin secreted from type II alveolar cells, since they did not express napsin mRNA. Conversely, immunoreactivity for napsin was undetectable in B lymphocytes with intense mRNA expression. In puromycin- or doxorubicin-induced proteinuria, napsin mRNA expression was markedly elevated in renal proximal tubules, showing characteristic distribution patterns. Immunostaining of kidneys with proteinuria showed intense immunoreactivity for napsin in congested and enlarged lysosomes, called protein absorption droplets. These results indicate that napsin functions as a lysosomal protease and is involved in protein catabolism in renal proximal tubules.
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PMID:Immunohistochemical localization of napsin and its potential role in protein catabolism in renal proximal tubules. 1250 93

Whereas intact antibody to rat kidney (7S) produced immediate and sustained proteinuria in rats, univalent fragments (papain digests) of the antibody did not, and divalent fragments (pepsin digests) produced only transitory proteinuria. The antibody fragments differed from the intact antibody in fixing little, if any, complement in vivo which may explain why they did not cause serious renal damage.
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PMID:Antibody to Rat Kidney: In vivo Effects of Univalent and Divalent Fragments. 1779 46