Autoradiographic patterns of [3H]uridine incorporation during the development of the mollusc, Acmaea scutum

Development ◽  
1973 ◽  
Vol 29 (1) ◽  
pp. 15-25
Author(s):  
Gerald C. Karp

Autoradiographic experiments on eggs and embryos of the gastropod mollusc, Acmaea scutum, have provided information on the time of initiation of [3H]uridine incorporation into RNA, the relative degree to which different embryonic regions are participating, and the relative rates of incorporation at different times of development. The unfertilized egg does not incorporate exogenous [3H]uridine. After fertilization the first indication of incorporation in the stages examined was at the beginning of the sixth cleavage. There is a marked increase in the level of incorporation during the sixth cleavage which marks the beginning of gastrulation in these embryos. After this stage there is a gradual increase in incorporation per embryo, throughout development to the mid-veliger. Very little indication of significant differences in the level of incorporation among the cells of any embryo was found. The most pronounced exception was the lower activity of the anterior ectodermal cells of the trochophore larva. At later stages the derivatives of these cells were as active as the cells of other regions.

1993 ◽  
Vol 58 (12) ◽  
pp. 2987-2993 ◽  
Author(s):  
Jarmila Vinšová ◽  
Karel Kosař ◽  
Evžen Kasafírek

A series of chiral spirocyclic cyclodipeptides of the general formula I was synthesized; the aim was to determine how the substitution of cyclobutane for cyclopentane in cyclo(-alanyl-1-amino-1-cyclopentanecarbonyl-) would influence the inhibition of the proliferative activity of the caudal morphogenic system (CMS) of Chick embryos. Spirocyclic cyclodipeptides Ia - Il were obtained by cyclization of linear dipeptides IIa - IIf, prepared by condensation of protected amino acids by DCCI method. The inhibition was investigated by the Chick Embryotoxicity Screening Test. The results show generally lower activity in the tested series, as compared with derivatives containing 1-amino-1-cyclopentanecarboxylic acid.


1986 ◽  
Vol 41 (9-10) ◽  
pp. 951-955 ◽  
Author(s):  
Hannu Elo ◽  
Paavo Lumme

Several derivatives and analogs of the recently reported antiproliferative and antitumor agent trans-bis(salicylaldoximato) copper(II) (CuSAO2) have been prepared and tested for antiproliferative activity against L1210 leukemia cells in vitro. The salicylaldimine analog of CuSAO2 had a very strong antiproliferative activity, the 2-day IC50 value being lower than 3 μg/ml- The 2,3-dihydroxybenzaldoxime analog was equally active with CuSAO2, while the corresponding 2,5-dihydroxy derivative had a slightly lower activity. The 2,3,4-trihydroxybenzaldoxime derivative had a much lower activity than had the dihydroxybenzaldoxime derivatives. The zinc(II) analog of CuSAO2 had only a low antiproliferative activity. The ligand of CuSAO2, salicylaldoxime, resembles pyridoxal oxime, a vitamin B6 antagonist and a powerful inhibitor of pyridoxal kinase. An attempt to reduce the toxicity of CuSAO2 in vivo with pyridoxal hydrochloride led to increased toxicity.


1982 ◽  
Vol 85 (1) ◽  
pp. 257-263 ◽  
Author(s):  
A. Graja ◽  
M. Przybylski ◽  
B. Butka ◽  
R. Swietlik

2002 ◽  
Vol 23 (2) ◽  
pp. 125-207 ◽  
Author(s):  
Igor D. Sadekov ◽  
Alexander V. Zakharov ◽  
Alexander A. Maksimenko
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document