Effect of vasectomy on hepatic drug metabolism

Summary 2 months after bilateral vasectomy the metabolism of aniline but not aminopyrine was increased in rat liver homogenates, whereas vasectomy did not affect the metabolism of either compound in guinea-pig liver homogenates.Supported by a grant from the University of Nebraska Medical Center.     

Effect of growth factors on hepatic drug metabolism in diabetic-hypophysectomized rats

Summary In vivo administration to diabetic-hypophysectomized rats of either the growth factor produced by the plerocercoid larvae of the tapeworm, Spirometra mansonoides, or mammalian growth hormone caused inhibition of hepatic drug metabolism measured in vitro.     

The effect of oxine-5-sulphonic acid on the hepatic drug metabolism in the rat

Summary Oxine-5-sulphonic acid inhibits the metabolism of aminopyrine in the rat liver in vitro. The characteristics of this inhibition vary according to whether the oxidativeN-demethylation of the substrate is determined by the formation of the metabolite 4-aminoantipyrine or by the production of formaldehyde.     

Diphasic action of 2,2-diphenylpropionic acid N,N-diethylaminoethyl ester hydrochloride on hepatic drug metabolism in the mouse

Summary 2,2-Diphenylpropionic acid N,N-diethylaminoethyl ester hydrochloride, 30 min after a single i.p. dose, inhibits the microsomal drug-metabolizing enzymes of the mouse liver and prolongs the hexobarbital sleeping time; 24 h after the administration, it induces hepatic microsomal drug-metabolizing enzymes and shortens hexobarbital sleeping time.     

Effect of praseodymium on drug metabolism in rat liver smooth and rough endoplasmic reticulum

Summary A small i.v. dose (3 mg/kg) of a light lanthanon, praseodymium, impairs the drug metabolizing capacity of both the smooth and rough fractions of rat liver endoplasmic reticulum. This decrease in the activity of drug metabolizing enzymes and in the amount of cytochromes P-450 and b₅ is more pronounced in the rough endoplasmic reticulum fraction.     

Cyclophosphamide-impaired regulation of hepatic heme metabolism

In male rats hepatic cytochromes b5 and P-450 were reduced at different times after treatment with cyclophosphamide (CP) (200 mg/kg i.p. for 3 days). In contrast, microsomal heme did not change until 48 h after the last dose of CP, leading to accumulation of heme in a 'non-cytochromal' form. Parallel to the above changes the heme metabolism showed derangement: delta-aminolaevulinate synthase, the rate-limiting enzyme in heme synthesis, was depressed and heme oxygenase, the enzyme which catalyzes the oxidative degradation of heme, was increased.     

Cyclophosphamide-impaired regulation of hepatic heme metabolism

Summary Im male rats hepatic cytochromes b₅ and P-450 were reduced at different times after treatment with cyclophosphamide (CP) (200 mg/kg i.p. for 3 days). In contrast, microsomal heme did not change until 48 h after the last dose of CP, leading to accumulation of heme in a non-cytochromal form. Parallel to the above changes the heme metabolism showed derangement: -aminolaevulinate synthase, the rate-limiting enzyme in heme synthesis, was depressed and heme oxygenase, the enzyme which catalyzes the oxidative degradation of heme, was increased.     

Effect of glucagon on lipid metabolism

Zusammenfassung Die Wirkung von Glukagon auf den Fettstoffwechsel gesunder Hunde wird untersucht. Intravenöse Verabreichung von 1 mg kristallinem Glukagon bewirkt weder im Serum-Cholesterin- noch im -Gesamt-lipidgehalt wesentliche Abweichungen und auch die Veränderung der Lipoproteinfraktionen ist nicht signifikant. Die Blutzuckerwerte sind bei sämtlichen Tieren stark erhöht.     

Influence of phenobarbital and TCDD on the hepatic metabolism of TCDD in the dog

The influence of phenobarbital and TCDD pretreatment on the formation and biliary excretion of TCDD-metabolites following single doses of 3H-TCDD was investigated. Without pretreatment, 24.5% of the absorbed 3H-TCDD dose was excreted in the bile within 110 h. Phenobarbital did not influence this rate, whereas a single dose of 10 micrograms of unlabeled TCDD/kg b.wt nine days earlier resulted in a doubling of the amount of radioactive material eliminated in the bile (47.4%).     

Influence of phenobarbital and TCDD on the hepatic metabolism of TCDD in the dog

Summary The influence of phenobarbital and TCDD pretreatment on the formation and biliary excretion of TCDD-metabolites following single doses of³H-TCDD was investigated. Without pretreatment, 24.5% of the absorbed³H-TCDD dose was excreted in the bile within 110 h. Phenobarbital did not influence this rate, whereas a single dose of 10 g of unlabeled TCDD/kg b.wt nine days earlier resulted in a doubling of the amount of radioactive material eliminated in the bile (47.4%).     

Behavioural consequences of vasectomy in the mouse

Summary Vasectomy was found to have no influence on the sexual activity of male mice. Testis and seminal vesicle weights were similary not influenced by this operation although a significant increase in epididymus weight was observed.J. C. is grateful to the Ford Foundation for financial support.     

Effect of emetine on certain aspects of protein metabolism

Résumé Le contenu de protéine, de RNA et de DNA dans les tissus de foie, de cur et de rognon a été étudié chez des rats albinos traités à l'émétine. Le traitement a réduit la concentration de la protéine et du DNA dans le foie et dans le rognon. Dans le cur, cette concentration ne fut pas altérée d'une maniére significative. On suggère que l'émétine non settlement empÊche la synthèse de la protéine, mais réduit aussi sa désagrégation.     

Effect of X-irradiation on triglyceride metabolism of the rabbit

Zusammenfassung Nach letaler Röntgenbestrahlung wurde eine Zunahme der Triglyceride, aber keine Veränderung der freien Fettsäuren im Kaninchenplasma gefunden. Eine Belastungsprobe mit I¹³¹ markierten Trioleins hat zu keiner Verhinderung der hepatischen Akkumulierung dieses Stoffes in den bestrahlten Tieren geführt. Der Befund weist darauf hin, dass nach Röntgenbestrahlung keine Störung des Fetttransportes aus dem Plasma resultiert, sondern dass die Lipämie eventuell durch abnorme Chylomicra zustande kommt.     

Effect of aminoglutethimide on murine fetal hepatic erythroid colony formation

Pretreatment of pregnant mice with aminoglutethimide phosphate, an inhibitor of glucocorticoid synthesis, increases the content of fetal liver erythroid colony-forming cells (CFU-E), as assessed by the formation of erythroid colonies in vitro by fetal liver cells in plasma clots containing exogenous erythropoietin. In addition, the inability of aminoglutethimide to influence erythroid colony formation in vitro suggests that endogenous glucocorticoids exert a suppressive effect on the number of functional CFU-E in the fetal liver.