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Enhancement of phagocytosis by Compound 48/80 and its influence upon Ca++-dependent ATP-ase.

作者信息

Falke D, Lemmel E M, Richardson L S, Wolf H U

出版信息

Arzneimittelforschung. 1975 Aug;25(8):1258-61.

PMID:170946
Abstract

A new activity of p-methoxy-phenylethyl-methyl-amine condensed by formaldehyde (Cpd 48/80) has been established: enhancement of phagocytosis. This property seems to be correlated to its ability to activate lysosomes. Enhancement of phagocytosis is discussed in relation to the virus penetration process. Furthermore it was found that Cpd 48/80 and to a smaller degree the dimer inhibit the Ca++-dependent ATP-ase (E. C. 3.6.1.3.) from human red blood cells. The enzyme from bovine myosin is not inhibited by the dimer, but somewhat more by poly-THIQ (7-methoxy-tetrahydroisoquinoline condensed by formaldehyde) than by Cpd 48/80. These properties are discussed in relation to a general hypothesis of virus-induced giant cell formation. Finally it has been shown that the drug does not influence the PHA-stimulation (phytohemagglutinin) of lymphocytes, indicating selectivity of its activity.

摘要

相似文献

1
Enhancement of phagocytosis by Compound 48/80 and its influence upon Ca++-dependent ATP-ase.
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引用本文的文献

1
Modulation of phagocytosis and intracellular bactericidal activity of polymorphonuclear and mononuclear cells by cationic proteins from human granulocytes: alternative pathway of phagocytic enhancement.人粒细胞阳离子蛋白对多形核细胞和单核细胞吞噬作用及细胞内杀菌活性的调节:吞噬增强的替代途径
Inflammation. 1984 Dec;8(4):445-57. doi: 10.1007/BF00918219.
2
Inhibition of giant cell formation by Compound 48-80 after infection with herpesvirus hominis. III. Binding of tritium-labelled Compound 48-80 to normal and infected cells and its action upon phosphatidyl-choline-biosynthesis.
Arch Gesamte Virusforsch. 1974;46(1-2):127-39. doi: 10.1007/BF01240212.
3
Inhibition of bone resorption in vitro by compound 48/80.化合物48/80对体外骨吸收的抑制作用。
Calcif Tissue Int. 1985 Jul;37(4):447-9. doi: 10.1007/BF02553717.