Novel method to produce a layered 3D scaffold for human pluripotent stem cell-derived neuronal cells.

Background: Three-dimensional (3D) in vitro models have been developed into more in vivo resembling structures. In particular, there is a need for human-based models for neuronal tissue engineering (TE). To produce such a model with organized microenvironment for cells in central nervous system (CNS), a 3D layered scaffold composed of hydrogel and cell guiding fibers has been proposed.

Development of hexagonal maze procedure for evaluating memory in rat.

Memory is known as a series of behavioral changes caused by an experience, while learning is a process for acquiring memory. In the present study, we suggested a new method (hexagonal maze) to evaluate the learning and memory of rats. For preliminary validation, the authors used the maze to carry out two classical experiments.

Role of soluble guanylate cyclase in reactivation of choline esterase inhibited by phosphoorganic compounds.

The effects of possible activators of soluble guanylate cyclase were studied. Hydroxylamine and some oxime derivatives such as pyridinium aldoximes and bispyridinium dioxime (dipyroxime) were tested as possible guanylate cyclase activators. These compounds are known to be reactivators of choline esterase which has been preinhibited with phosphoorganic compounds.

Mechanism of activation of soluble guanylate cyclase by guanidine thiols--a new class of enzyme activators.

The study is concerned with the mechanism of activation of soluble guanylate cycla-se by guanidine thiol derivatives-a new class of enzyme activators. Guanidine thiols contain both the guanidine and SH group which act, respectively, as donor and acceptor of nitric oxide (NO). The role of guanidine thiol SH group in the mechanism of soluble guanylate cyclase activation was studied.

Guanidine thiol--a new activator of soluble guanylate cyclase with antihypertensive and antiaggregatory properties.

Effects of aminoethylisothiuronium bromide (AET), known as radioprotector, on human platelet soluble guanylate cyclase and on ADP-induced human platelets aggregation were studied. It was shown that AET - in Tris buffer and at certain pH values - is converted, via transguanidine rearrangement, to mercaptoethylguanidine. The latter contains in its molecule both the guanidine and SH groups which act as donor and acceptor of nitric oxide (NO), respectively.