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1.
Klin Wochenschr ; 67(8): 442-6, 1989 Apr 17.
Article in German | MEDLINE | ID: mdl-2657206

ABSTRACT

The technical evolution of ultrasonic equipment provides a high resolution imaging analysis of the vessel wall and thereby offers new possibilities in diagnosing very early atherosclerotic changes. The typical B-mode image in human and animal arteries shows parallel wall contures enclosing a hypoechoic space. In this study in Vitro- and in Vivo-experiments in rabbit aortas document the distance between these contures correlating histologically with a high cholesterol diet caused a broadening of the hypoechoic space in the rabbit aortic vessel wall. The data demonstrate that high resolution Duplex Sonography is a usefull noninvasive approach for the detection of very early atherosclerotic changes in arterial vessel walls in a stage before plaques can be identified.


Subject(s)
Arteriosclerosis/diagnosis , Ultrasonography , Animals , Aorta/pathology , Diet, Atherogenic , Endothelium, Vascular/pathology , Muscle, Smooth, Vascular/pathology , Rabbits
2.
Parasitol Res ; 75(5): 353-60, 1989.
Article in English | MEDLINE | ID: mdl-2657716

ABSTRACT

The seleno-organic compound ebselen showed anti-malarial activity in vitro against the murine Plasmodium berghei and the human P. falciparum. In P. berghei, the uptake and incorporation of [3H]-methionine and [3H]-adenosine was inhibited and the infectivity of plasmodia was reduced. Ebselen affects the development of asexual stages of chloroquine-resistant and -sensitive P. falciparum strains. Its IC50 for P. falciparum was about 14 mumol/l and that for P. berghei, about 10 mumol/l. The growth of P. falciparum was blocked by ebselen at all stages, including the invasion of erythrocytes by merozoites. In a human hepatoma cell line and in mouse peritoneal macrophages, no cytostatic or cytotoxic effects were found, indicating selective inhibition of plasmodia by ebselen. Its in vitro inhibitory effect is discussed in relation to its possible reactivity with thiol groups and its lack of an anti-malarial effect in infected mice.


Subject(s)
Antimalarials/pharmacology , Antioxidants/pharmacology , Azoles/pharmacology , Organoselenium Compounds , Plasmodium berghei/drug effects , Plasmodium falciparum/drug effects , Selenium/pharmacology , Animals , Antimalarials/toxicity , Antioxidants/toxicity , Azoles/toxicity , Cell Line , Humans , Isoindoles , Macrophages/drug effects , Malaria/drug therapy , Male , Mice , Molecular Structure , Pyrimethamine/pharmacology , Quinacrine/pharmacology , Selenium/toxicity
3.
Atherosclerosis ; 69(2-3): 155-60, 1988 Feb.
Article in English | MEDLINE | ID: mdl-3348838

ABSTRACT

Octimibate sodium (8-[(1,4,5-triphenyl-1H-imidazol-2-yl)oxy]octanoic acid, sodium salt; NAT 04-152) was investigated for its antihyperlipidemic and antiatherosclerotic activities in New Zealand White rabbits. Hypercholesterolemia and atherosclerosis were induced by feeding a diet containing 0.3% cholesterol for 8 weeks. In addition, repeated injections of bovine serum albumin (BSA) were used to enhance the experimental atherosclerosis. Octimibate sodium, 10.0 and 30.0 mg/kg p.o., reduced both the increase in serum cholesterol levels and the aortic plaque-formation (by about 50% in the higher dose group) as compared to control animals. Serum triglyceride levels were not influenced. Biochemical and histological examinations of the aortas showed reduced cholesterol contents in the higher dose group and a dose-dependent inhibition of pathological changes in the aortas.


Subject(s)
Arteriosclerosis/drug therapy , Caprylates/therapeutic use , Hypercholesterolemia/drug therapy , Hypolipidemic Agents/therapeutic use , Imidazoles/therapeutic use , Animals , Diet, Atherogenic , Rabbits , Serum Albumin, Bovine , Sterol O-Acyltransferase/antagonists & inhibitors
4.
Tropenmed Parasitol ; 32(1): 51-4, 1981 Mar.
Article in German | MEDLINE | ID: mdl-6785913

ABSTRACT

Strains of low virulent Trypanosoma cruzi are difficult to maintain in experimental hosts, but they can be activated by the immunosuppressive effects of cyclophosphamide (CY), a cancer chemotherapeutic agent. An attempt, using electron microscopy, to find out whether CY had any effect on the morphology of the bloodstream forms of the parasite failed to detect any differences when those from CY-treated hosts were compared with those from controls.


Subject(s)
Chagas Disease/parasitology , Cyclophosphamide/pharmacology , Trypanosoma cruzi/drug effects , Animals , Blood/parasitology , Female , Mice , Microscopy, Electron , Organoids/ultrastructure , Trypanosoma cruzi/ultrastructure
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