Search Results

You are looking at 1 - 2 of 2 items for

  • Author or Editor: A Baranowska x
Clear All Modify Search

Abstract  

The kinetic parameters of thermal decomposition of Cu(II) and Zn(II) salts of carboxylic acids were investigated on the basis of the respective thermal curves. The values of the activation energy (E a) of thermal decomposition, reaction order (n), frequency factor (A) and velocity constant (k) (in the Arrhenius kinetic equation), established from thermal data, were compared. Based on the initial decomposition temperature, the following sequences of stabilities of the studied compounds have been proposed: 1.  Cu(CH3COO)2 (235°)>Cu(C6H5O7)2 (220°)>Cu(HCOO)2 (150°)>>Cu(OH)2·Cu(CO3) (50°) 2.  Zn(C18H35O2)2 (305°)>ZnCO3 (210°)>Zn(CH3COO)2 (170°)

Restricted access

The purpose of this study was to determine the activity of the autonomic nervous system (ANS), using spectral analysis of the heart rate variability (HRV) in the model of partial bladder outlet obstruction (PBOO) in rats treated with selected non-steroidal anti-inflammatory drugs (NSAID): piroxicam (PRX) or meloxicam (MLX), and following administration of PGF2a prostaglandin analogue (Enzaprost F5). Neither the use of PGF2a analogue nor of MLX, caused significant changes in the HRV spectrum (except for HRV spectrum total power reduction with MLX). The use of PRX caused reduction of the total power and powers of all components of the HRV spectrum (except for VLF). Moreover, increased nLF and reduced nHF were observed. The obtained results suggest that the total prostaglandin synthesis block with a non-selective cyclooxygenase inhibitor (PRX) results in reduced ANS total activity, with decreased parasympathetic activity and a relative sympathetic predominance. The preferential cyclooxygenase-2 block (MLX) caused reduction of the total ANS activity as well, however with no clear disproportion of any part of the ANS. Therefore, prostaglandin synthesis inhibition and associated decrease of parasympathetic activity may constitute an additional and favourable feature of NSAID pharmacodynamics in the treatment of BPH.

Restricted access