Evaluation of enzyme histochemical observations for metabolic studies. A combined histochemical and biochemical investigation of experimental induced muscle-changes

1973 ◽  
Vol 36 (1) ◽  
pp. 63-71 ◽  
Author(s):  
A. C. J�bsis ◽  
A. E. F. H. Meijer
Planta Medica ◽  
2012 ◽  
Vol 78 (11) ◽  
Author(s):  
JL Giner ◽  
GH Wikfors ◽  
RP Hassett
Keyword(s):  

1968 ◽  
Vol 19 (03/04) ◽  
pp. 383-388 ◽  
Author(s):  
R Losito ◽  
C. A Owen ◽  
E. V Flock ◽  

SummaryThe metabolism of vitamin K1- 14C and menadione-14C (vitamin K3-14C) was studied in normal and hepateetomized rats. After the administration of menadione, about 70% of the 14C was excreted in the urine in 24 hrs in both types of rats. Two urinary metabolites were identified by enzymatic hydrolysis: one a glucuronide and the other a sulfate of reduced menadione. Thus, the liver is not necessary for the metabolism of menadione. In the vitamin K1 studies, the intact rats excreted only 10% of the 14C and the hepatectomized rats excreted less than 0.5%. The retention of vitamin K1 may explain its superiority over menadione as an antidote for overdosages of oral anticoagulants.


1961 ◽  
Vol 38 (3) ◽  
pp. 413-418 ◽  
Author(s):  
S. Almqvist ◽  
D. Ikkos ◽  
R. Luft

ABSTRACT The effect of graded doses (5, 10 and 25 mg/d of methandrostenolone and of 25 mg/d of testosterone propionate were compared in each of three metabolically stable adult subjects. Five mg/d of methandrostenolone induced nitrogen and calcium retention. The effects observed with larger doses of methandrostenolone (10 and 25 mg/d) were not quantitatively different from those with 5 mg/d. The nitrogen and calcium retention obtained with the daily dose of 5 mg of methandrostenolone was as great or greater than that induced by testosterone propionate (25 mg/d). Methandrostenolone induced creatinuria but had no effect on sodium and chloride balances and urinary excretion of 17-ketosteroids.


1940 ◽  
Vol 43 (3) ◽  
pp. 470-473 ◽  
Author(s):  
A. T. Milhorat ◽  
F. C. Weber ◽  
V. Toscani
Keyword(s):  

1940 ◽  
Vol 134 (2) ◽  
pp. 567-572
Author(s):  
Richard J. Block ◽  
George A. Jervis ◽  
Diana Bolling ◽  
Merrill Webb
Keyword(s):  

1954 ◽  
Vol 207 (1) ◽  
pp. 287-294
Author(s):  
Paul M. Hyde ◽  
William H. Elliott ◽  
E.A. Doisy ◽  
Edward A. Doisy
Keyword(s):  

Metabolites ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 404
Author(s):  
Gabriela de Matuoka e Chiocchetti ◽  
Leisa Lopes-Aguiar ◽  
Natália Angelo da Silva Miyaguti ◽  
Lais Rosa Viana ◽  
Carla de Moraes Salgado ◽  
...  

Cancer cachexia is a severe wasting condition that needs further study to find ways to minimise the effects of damage and poor prognosis. Skeletal muscle is the most impacted tissue in cancer cachexia; thus, elucidation of its metabolic alterations could provide a direct clue for biomarker research and be applied to detect this syndrome earlier. In addition, concerning the significant changes in the host metabolism across life, this study aimed to compare the metabolic muscle changes in cachectic tumour-bearing hosts at different ages. We performed 1H-NMR metabolomics in the gastrocnemius muscle in weanling and young adult Walker-256 tumour-bearing rats at different stages of tumour evolution (initial, intermediate, and advanced). Among the 49 metabolites identified, 24 were significantly affected throughout tumour evolution and 21 were significantly affected regarding animal age. The altered metabolites were mainly related to increased amino acid levels and changed energetic metabolism in the skeletal muscle, suggesting an expressive catabolic process and diverted energy production, especially in advanced tumour stages in both groups. Moreover, these changes were more severe in weanling hosts throughout tumour evolution, suggesting the distinct impact of cancer cachexia regarding the host’s age, highlighting the need to adopting the right animal age when studying cancer cachexia.


1940 ◽  
Vol 134 (1) ◽  
pp. 105-113
Author(s):  
George A. Jervis ◽  
Richard J. Block ◽  
Diana Bolling ◽  
Edna Kanze
Keyword(s):  

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