[Changes of the neuropil ultrastructure in the CA1 hippocampal area of rat pups after hyaluronidase treatment].

Electron microscopical and electrophysiological studies were carried out in cross-sections of the hippocampus of 4-weeks-old male rat pups (n = 35) to detect the ultrastructural changes in CA1 hippocampal area and the peculiarities of excitatory postsynaptic potential formation in this brain area after the incubation of the sections in the solution of hyaluronidase (10 U/ml), the enzyme which specifically degrades the extracellular matrix glycosaminoglycan--the hyaluronic acid. The reduction of the width of synaptic cleft by 15-25% in the axo-dendritic contacts of the stratum radiatum of CA1 hippocampal area was detected 1.5 min following the application of enzyme, coinciding with the increase of the excitatory postsynaptic potential amplitude.

[Comparisons of brain weight and neocortical thickness in 21-day-old fetuses and 1-day-old rats with the histophysiological indices of the ovaries and adrenal glands of their mothers (a correlational and cluster analysis)].

The correlation and cluster analysis revealed that the brain weight of the rat 21-day-old foetus obviously depended on 3 beta-hydroxysteroiddehydrogenase activity in adrenal cortex. No such dependence was found in 1-day-old foetus. Thickness of the brain cortex in 21-day-old foetus and in 1-day-old rat correlated with parameters of the enzyme activity in the corpus luteum, corpus atretic, and theca folliculi of mother's ovaries.

[Construction of plasmids coding for diphtheria toxin fragments].

Plasmids coding different nontoxic derivatives (toxoids) of the diphtheria toxin were constructed. A secretion of toxoids that carry a signal sequence was found in the periplasmic space of E. coli and Erwinia carotovora.

[Construction of derivatives of the diphtheria toxin gene and their expression in Escherichia coli cells].

A fragment of diphtheria toxin (tox) gene from beta 45 phage DNA was cloned on pUC19 plasmid in E. coli cells. The fragment is coding for toxA fragment of the toxin and contains the control region of the tox gene.