scholarly journals Strategy and choice criteria’s of initial disturbances of brain circulation in family physician’s practice

2021 ◽  
pp. 12-15
Author(s):  
S. G. Burchinsky

In the present paper a modern sights to manifestations of initial stages of brain ischemia and its role in damage of CNS in cerebrovascular pathology have been looked. Based on this point of view, the requirements to choice of optimal pharmacological strategy concerning correction of brain pathological changes during ischemia, and particularly neurometabolic pharmacotherapy’ advantages have been analyzed. A basic goals of clinical use of neuroprotection’s strategy in generally, and particularly neurometabolic pharmacotherapy have been looked. A main attention paid to mechanisms of action and peculiarities of clinical use of drug Dinar (ethyl-methyl-hydroxypiridine succinat) and its possibilities in plane to realization of pathogenetically grounding neurometabolic pharmacotherapy of initial stages of cerebrovascular pathology. A clinical efficacy of Dinar and its safety characteristics have been looked in detail.

2016 ◽  
pp. 50-54
Author(s):  
Serhii Burchinsky

In the present paper a modern sights to problem of neurometabolic pharmacotherapy looking on correction of neuronal metabolism in clinical practice have been looked. Based on this point of view, the requirements to choice of optimal pharmacological tool of this strategy have been analyzed. A main attention paid to mechanisms of action and peculiarities of clinical use of drug Mexiprim (ethyl-methyl-hydroxypiridine succinat) with unique pharmacological and clinical properties, that make possible to realize the strategy of pathogenetically grounded neurometabolic pharmacotherapy in treatment of cerebrovascular disturbances, and other forms of pathology. A clinical efficacy of Mexiprim and its safety characteristics have been analyzed.


2021 ◽  
pp. 14-18
Author(s):  
S. G. Burchinsky

In the present paper a modern sights to problem of chronic psychogenic pain and its relation to depressive and anxiety disorders have been looked. Based on this point of view, the requirements to choice of optimal pharmacological tool within complex therapy of psychogenic pain, depression and anxiety have been analyzed. A main attention paid to mechanisms of action and peculiarities of clinical use of drugs: duloxetine (Revival) – antidepressant from SNRI group with unique mechanisms of action and clinico-pharmacological properties, which make possible to realize the on-time impact on the mechanisms of development of depression and psychogenic pain; and pregabaline (Ligato) – drug from the anticonvulsants group, which influenced on universal mechanisms of cell ionic permeability at anxiety disorders and psychogenic pain. A clinical efficacy of duloxetine (Revival) and pregabaline (Ligato), its safety characteristics, and recommendations of practical use have been looked in detail.


2021 ◽  
Vol 16 (8) ◽  
pp. 37-42
Author(s):  
S.G. Burchinsky

The article considers modern views on the problem of vascular cognitive dysfunction, in particular, on the nature and options of treatment of mild cognitive impairment syndrome as one of the most common forms of cognitive decline in the elderly and senile patients. From this point of view, the requirements for the selection of the optimal pharmacological tool for pharmacotherapy and pharmacoprophylaxis of this syndrome, especially the strategy of membrane protection, are analyzed. Particular attention is paid to the mechanisms of action and features of clinical use of Lira (citicoline) — a drug with unique clinical and pharmacological properties that allow implementing a strategy of pathogenetically sound neuro- and geroprotective pharmacotherapy in cerebrovascular disorders. Mechanisms of action, clinical efficacy of Lira (citicoline), safety characteristics and recommendations for practical use of the drug are considered in detail.


2021 ◽  
Vol 22 (8) ◽  
pp. 4203
Author(s):  
Giorgio Valabrega ◽  
Giulia Scotto ◽  
Valentina Tuninetti ◽  
Arianna Pani ◽  
Francesco Scaglione

Poly(ADP-ribose) polymerases (PARP) are proteins responsible for DNA damage detection and signal transduction. PARP inhibitors (PARPi) are able to interact with the binding site for PARP cofactor (NAD+) and trapping PARP on the DNA. In this way, they inhibit single-strand DNA damage repair. These drugs have been approved in recent years for the treatment of ovarian cancer. Although they share some similarities, from the point of view of the chemical structure and pharmacodynamic, pharmacokinetic properties, these drugs also have some substantial differences. These differences may underlie the different safety profiles and activity of PARPi.


2007 ◽  
Vol 1117 (1) ◽  
pp. 209-257 ◽  
Author(s):  
R. G. G. RUSSELL ◽  
Z. XIA ◽  
J. E. DUNFORD ◽  
U. OPPERMANN ◽  
A. KWAASI ◽  
...  

1998 ◽  
Vol 79 (5) ◽  
pp. 388-391
Author(s):  
G. V. Cherepnev ◽  
Y. D. Slabnov ◽  
I. E. Zimakova

The relevance of pharmacological correction of immunological reactivity is obvious: many socially significant diseases are accompanied by an imbalance in immune homeostasis. In the past few years, a number of reviews on the classification and mechanisms of action of immunotropic drugs approved for clinical use in the Russian Federation have been published in the domestic press.


2012 ◽  
Vol 142 (1) ◽  
pp. 15-24 ◽  
Author(s):  
Jens Ingwersen ◽  
Orhan Aktas ◽  
Patrick Kuery ◽  
Bernd Kieseier ◽  
Alexey Boyko ◽  
...  

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