Detailed Information on Publication Record
2017
Pharmacological modulation of radiation damage. Does it exist a chance for other substances thanhematopoietic growth factors and cytokines?
HOFER, Michal, Z HOFEROVÁ and Martin FALKBasic information
Original name
Pharmacological modulation of radiation damage. Does it exist a chance for other substances thanhematopoietic growth factors and cytokines?
Authors
HOFER, Michal, Z HOFEROVÁ and Martin FALK
Edition
International Journal of Molecular Sciences, Basel, Multidisciplinary Digital Publishing Institute, 2017, 1422-0067
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.687
UT WoS
000408746800057
Tags
International impact, Reviewed
Změněno: 19/12/2019 13:42, doc. RNDr. Martin Falk, Ph.D.
Abstract
V originále
In recent times, cytokines and hematopoietic growth factors have been at the center of attention for many researchers trying to establish pharmacological therapeutic procedures for the treatment of radiation accident victims. Two granulocyte colony-stimulating factor-based radiation countermeasures have been approved for the treatment of the hematopoietic acute radiation syndrome. However, at the same time, many different substances with varying effects have been tested in animal studies as potential radioprotectors and mitigators of radiation damage. A wide spectrum of these substances has been studied, comprising various immunomodulators, prostaglandins, inhibitors of prostaglandin synthesis, agonists of adenosine cell receptors, herbal extracts, flavonoids, vitamins, and others. These agents are often effective, relatively non-toxic, and cheap. This review summarizes the results of animal experiments, which show the potential for some of these untraditional or new radiation countermeasures to become a part of therapeutic procedures applicable in patients with the acute radiation syndrome. The authors consider β-glucan, 5-AED (5-androstenediol), meloxicam, γ-tocotrienol, genistein, IB-MECA (N6-(3-iodobezyl)adenosine-5’-N-methyluronamide), Ex-RAD (4-carboxystyryl-4-chlorobenzylsulfone), and entolimod the most promising agents, with regards to their contingent use in clinical practice.
Links
GA16-12454S, research and development project |
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NV16-29835A, research and development project |
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