Radioactive Tracers in the Study of Energy Turnover by a Grazing Insect (Chrysochus auratus Fab.; Coleoptera Chrysomelidae)

Oikos ◽  
1968 ◽  
Vol 19 (1) ◽  
pp. 10 ◽  
Author(s):  
Eliot C. Williams ◽  
David E. Reichle
Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4221
Author(s):  
Aage Kristian Olsen Alstrup ◽  
Svend Borup Jensen ◽  
Ole Lerberg Nielsen ◽  
Lars Jødal ◽  
Pia Afzelius

The development of new and better radioactive tracers capable of detecting and characterizing osteomyelitis is an ongoing process, mainly because available tracers lack selectivity towards osteomyelitis. An integrated part of developing new tracers is the performance of in vivo tests using appropriate animal models. The available animal models for osteomyelitis are also far from ideal. Therefore, developing improved animal osteomyelitis models is as important as developing new radioactive tracers. We recently published a review on radioactive tracers. In this review, we only present and discuss osteomyelitis models. Three ethical aspects (3R) are essential when exposing experimental animals to infections. Thus, we should perform experiments in vitro rather than in vivo (Replacement), use as few animals as possible (Reduction), and impose as little pain on the animal as possible (Refinement). The gain for humans should by far exceed the disadvantages for the individual experimental animal. To this end, the translational value of animal experiments is crucial. We therefore need a robust and well-characterized animal model to evaluate new osteomyelitis tracers to be sure that unpredicted variation in the animal model does not lead to a misinterpretation of the tracer behavior. In this review, we focus on how the development of radioactive tracers relies heavily on the selection of a reliable animal model, and we base the discussions on our own experience with a porcine model.


ACS Nano ◽  
2021 ◽  
Vol 15 (2) ◽  
pp. 3212-3227
Author(s):  
Elisa Lázaro-Ibáñez ◽  
Farid N. Faruqu ◽  
Amer F. Saleh ◽  
Andreia M. Silva ◽  
Julie Tzu-Wen Wang ◽  
...  

1975 ◽  
Vol 15 (5) ◽  
pp. 235-250
Author(s):  
L. C. J. Baghuis ◽  
M. Prins ◽  
H. L. Hagedoorn ◽  
J. A. V. D. Heide

Obesity ◽  
2021 ◽  
Author(s):  
Anja Bosy‐Westphal ◽  
Franziska A. Hägele ◽  
Manfred J. Müller
Keyword(s):  

1951 ◽  
Vol 29 (2) ◽  
pp. 123-132 ◽  
Author(s):  
William T. Foley ◽  
Paul A. Giguère

A precision freezing point apparatus with platinum resistance thermometer was used to investigate the system hydrogen peroxide – water over the whole concentration range. The freezing point of the purest sample of hydrogen peroxide obtained by repeated fractional crystallizations of a large quantity of 99.6% pure solution was found to be −0.461°C; that of the dihydrate was −52.10°C. The two eutectics occur at concentrations of 45.2% and 61.2% H2O2 and at temperatures of −52.4° and −56.5°C. respectively. Contrary to what has been reported previously, water and hydrogen peroxide do not form solid solutions together. This was proved conclusively by applying the technique of radioactive tracers to the 'wet residue' method of Schreinemakers.


1984 ◽  
Vol 56 (2) ◽  
pp. 520-525 ◽  
Author(s):  
G. A. Brooks ◽  
C. M. Donovan ◽  
T. P. White

o assess the effects of gradient and running speed on efficiency of exercise, and to evaluate contributions of oxidative and anaerobic energy production (Ean) during locomotion, two sets of experiments were performed. The caloric expenditures of rats were determined from O2 consumption (VO2) while they ran at three speeds (13.4, 26.8, and 43.1 m/min) on five grades (1, 5, 10, 15, and 20%). In addition, lactate turnover (LaT) and oxidation (Laox) were determined on rats at rest or during running at 13.4 and 26.8 m/min on 1% grade, respectively. Lactate production not represented in the VO2 (i.e., Ean) was calculated from the LaT not accounted for by oxidation [(LaT an) = LaT-Laox)]. The Ean was calculated as: Ean = [LaT an(mumol/min)] [1.38 ATP/La] [11 mcal/mumol ATP]. Gross efficiency of exercise (the caloric equivalent of external work/caloric equivalent of VO2 X 100) ranged from 1.7 to 4.5%. Apparent efficiency (the inverse of the regression of caloric equivalent of VO2 on the caloric equivalent of work X 100) ranged from 20.5 to 26.4% and reflected the metabolic response of rats to applied external work. The contribution of Ean to total energy turnover ranged from 1.6% at rest to 0.8% during running at 13.4 m/min on a 1% grade. Despite active LaT during steady-state exercise, Ean contributes insignificantly to total energy transduction, because over 70% of the lactate produced is removed through oxidation. VO2 adequately represents metabolism under these conditions.


1958 ◽  
Vol 137 (3) ◽  
pp. 363-388 ◽  
Author(s):  
J. L. Sirlin ◽  
R. G. Edwards

1999 ◽  
Vol 54 (1) ◽  
pp. 91-101 ◽  
Author(s):  
V. Blet ◽  
Ph. Berne ◽  
C. Chaussy ◽  
S. Perrin ◽  
D. Schweich

2004 ◽  
Vol 555 (1) ◽  
pp. 27-43 ◽  
Author(s):  
Timothy G. West ◽  
N. A. Curtin ◽  
Michael A. Ferenczi ◽  
Zhen-He He ◽  
Yin-Biao Sun ◽  
...  

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