The Inhibitory Action of Insulin in the Early Chick Embryo

Development ◽  
1962 ◽  
Vol 10 (1) ◽  
pp. 88-98
Author(s):  
Patricia Barron ◽  
J. Mckenzie

The list of effective teratogenic agents has become embarrassingly long: physical agents, metabolic inhibitors, vitamin deficiency, hypervitaminosis, and hormones, to mention only a few, are all known to produce congenital abnormalities. These substances have been administered at different times and in varying doses to nearly every group of animals, from amphibians to mammals, but there has been little effort to examine their mode of action. All too often, investigation ceases with the demonstration of a statistically significant number of abnormalities, enough to label the agent teratogenic. Sometimes a section of the work describes the histology of the lesions but does not indicate the primary action of the teratogen. Occasionally a drug has a well-recognized metabolic or chemical effect, e.g. cyanide on cytochrome oxidase, iodoacetate on triosephosphate dehydrogenase (Spratt, 1950), and we learn, by deduction, a little of the normal metabolism of development. Relatively few substances fall into this category, however.

Development ◽  
1960 ◽  
Vol 8 (3) ◽  
pp. 314-320
Author(s):  
J. McKenzie ◽  
J. D. Ebert

Antimycin A, an antibiotic obtained from an undetermined species of streptomyces, was isolated, crystallized, and described by Dunshee, Leben, Keitt, & Strong (1949), and its biological action has been studied by many workers since then. Ahmad, Schneider, & Strong (1950) demonstrated its effects on the growth and metabolism of yeast, on enzyme activities in the succinoxidase system, and on rats given the drug orally. Potter & Reif (1952) confirmed the inhibitory effect of antimycin A on the succinoxidase system in liver, suggested the presence of an ‘antimycin A-blocked factor’, identical, probably, with the ‘Slater factor’ and showed that, in certain tissues, there is an antimycin A-insensitive pathway for DPN oxidation. The same workers, Reif & Potter (1954), used the drug to characterize the pathways of DPN oxidation in different tissues. Green, Mii, & Kahout (1955) and Thorn (1956) argue from their experiments that the BAL-sensitive (Slater) factor and the antimycin A-sensitive factor are not identical.


1946 ◽  
Vol 165 (1) ◽  
pp. 125-130
Author(s):  
Harry G. Albaum ◽  
Alex B. Novikoff ◽  
Maurice Ogur

Cells ◽  
2018 ◽  
Vol 7 (2) ◽  
pp. 9 ◽  
Author(s):  
José Serrado Marques ◽  
Vera Teixeira ◽  
António Jacinto ◽  
Ana Tavares

1948 ◽  
Vol 68 (2) ◽  
pp. 263-266 ◽  
Author(s):  
A. M. Schechtman

1988 ◽  
Vol 222 (1) ◽  
pp. 90-94 ◽  
Author(s):  
Masao Nakamura ◽  
Takashi Kuwana ◽  
Yukihiko Miyayama ◽  
Toyoaki Fujimoto

1945 ◽  
Vol 29 (2) ◽  
pp. 63-72 ◽  
Author(s):  
Ralph Holt Cheney

1. By means of the Warburg-Barcroft microrespirometer apparatus and the Warburg direct method, the relative effect of caffeine upon the O2 consumption of the fertilized egg of Arbacia punctulata was shown for the following concentrations in sea water: 0.002 per cent (M/10,000), 0.004 per cent (M/5,000), 0.02 per cent (M/1,000), 0.1 per cent (M/200), 0.2 per cent (M/100), 0.5 per cent (M/40), and 2 per cent (M/10). 2. In comparison with the normal eggs (uninhibited, non-caffeine-treated controls), caffeine in concentrations including and greater than 0.1 per cent (M/200) depressed the average uptake from approximately 25 to 61 per cent over the 3 hour period. In a number of instances, as typified by Experiment 10, the effective inhibitory concentration ranged from 0.02 per cent (M/1,000) upward and the degree of depression of the O2 consumption ranged from 10.6 per cent to 60.6 per cent. 3. All caffeine concentrations including and above 0.02 per cent (M/1,000) in the series used, resulted in decreasing the normal rate of cleavage division in the fertilized Arbacia eggs. 4. The higher concentrations (0.5 and 2 per cent) produced a complete blockage of the cleavage process. 5. Complete cleavage inhibition was noted only when the O2 uptake had been depressed to 50 per cent or more of the normal controls. 6. O2 consumption-time relationship data indicate an average depression, in O2 consumption over a 3 hour period, ranging from 25 per cent with a caffeine concentration of 0.1 per cent to a 61 per cent inhibition with a concentration of 2 per cent. 7. Concentrations of less than 0.1 per cent (certainly of less than 0.02 per cent) give variable results and indicate no significant effect. 8. It is inferred from the respiration data presented that it is probable that the inhibition of the O2 consumption in fertilized Arbacia eggs is due to the influence of caffeine upon the main (activity or primary) pathway. It will be observed that there are certain similarities of the caffeine data to the degree of inhibition accomplished by sodium cyanide. Moreover, it has been demonstrated that the cyanide probably acts on the cytochrome oxidase step in the cytochrome oxidase-cytochrome chain of reactions constituting the O2 uptake phase of respiratory metabolism. It is not improbable, therefore, that caffeine also may act upon the cytochrome oxidase enzyme. 9. From the viewpoint of environmental conditions influencing reproductive phenomena, it is of interest that caffeine can affect the normal metabolism of the zygote.


2008 ◽  
Vol 50 (6) ◽  
pp. 449-452 ◽  
Author(s):  
Jun Hatakeyama ◽  
Kenji Shimamura

Sign in / Sign up

Export Citation Format

Share Document