血管障害に占める腎皮質中の血管透過性因子の役割について
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The decisive role played by hypertension in the production of vascular lesions is well known. There is much argument as to whether endogenous pressor substances are able to produce vascular lesions. In our laboratory it has been clarified that a vascular permeability factor besides pressor factors is present in extracts of kidney cortex and might play an important role in the development of experimental cerebral hemorrhages in hypertensive rabbits caused by GOLD-BLATT technique. Thus the present studies were undertaken to investigate the biological and chemical properties of the vascular permeability factor obtained from human kidney cortex and its role in the pathogenesis of human vascular lesions, especially of cerebral hemorrhages. Materials and methods 1. Isolation of CPF in kidny tissue. Human kidneys obtained at autopsies were extensively perfused through a polyethylene tube inserted in the renal artery. The perfusion fluid was 10: 1 of saline added heparin. After the last traces of blood had been washed out medullar layer was removed and cortical layer cutted into small pieces which were washed with cold saline to eliminate the haemoglobin. The tissue was weighed and suspended in 2 vol. of the distilled water and then homogenized. The homogenates were kept over night in a cold room, and then centrifuged at 40000 × g for 30 minutes and the supernatant recentrifuged at 100000 g for 60 minutes. Sephadex G 100 and 1/50 M tris buffer were used for the gel filtration. 2. Preparation of antisera. The microsomal fraction isolated from human kidney cortex was treated with 0.5 per cent deoxycholate and was centrifuged at 105000 X g for 90 minutes. The supernatant thus obtained was separated into three sub-fractions by means of the fractional precipitation with ammonium sulphate. Sub-fraction 45 was dissolved with water and dialyzed against it. The antisere were obtained in rabbit using adjuvant technique.
- 社団法人日本循環器学会の論文
- 1967-09-15
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