Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro

Benzodiazepines (BDZs) are known to act not only in the central nervous system, but on peripheral cells and tissues binding to the peripheral-type benzodiazepine receptors. In the present study, the influence of two different BDZs (diazepam (Dz) and tofizopam (Tof)) on several immune functions has b...

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Main Authors: Sergey V. Kalashnikov, Elena A. Kalashnikova, Svetlana N. Kokarovtseva
Format: Article
Language:English
Published: Hindawi Limited 2002-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1080/09629350210309
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spelling doaj-9e1fd56369cd4c168f0c474d333aa2bc2020-11-24T21:24:40ZengHindawi LimitedMediators of Inflammation0962-93511466-18612002-01-01111535910.1080/09629350210309Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitroSergey V. Kalashnikov0Elena A. Kalashnikova1Svetlana N. Kokarovtseva2Medical Centre for Russian Federation President's Office, Michurinskii Avenue 6, Moscow, RussiaLaboratory of Immunogenetics, Research Centre for Medical Genetics, Moskvorechie Street 1, Moscow 115478, RussiaLaboratory of Immunogenetics, Research Centre for Medical Genetics, Moskvorechie Street 1, Moscow 115478, RussiaBenzodiazepines (BDZs) are known to act not only in the central nervous system, but on peripheral cells and tissues binding to the peripheral-type benzodiazepine receptors. In the present study, the influence of two different BDZs (diazepam (Dz) and tofizopam (Tof)) on several immune functions has been examined in vitro. Some differences between Dz and Tof in their effects on human lymphocyte proliferative response, changes in glucocorticoid-induced suppression of cell proliferation and influence on cytokine production (tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2)) have been determined. Dz suppressed mitogen-induced peripheral blood mononuclear cell (PBMC) proliferation, enhanced dexamethasone-induced inhibition of PBMC proliferative response, and suppressed lymphocyte production of TNF-α and IL-2. Tof usually enhanced PBMC proliferation and IL-2 production in low and moderate doses, but in high doses it suppressed both. Tof in all investigated doses enhanced dexamethasone-induced suppression of lymphocyte proliferation and depressed TNF-α production. Thus, both Dz and Tof are shown to have immunomodulating effects in vitro. Tof, opposite to Dz even in the therapeutic doses, is able to enhance in vitro mitogen-induced lymphocyte proliferation and IL-2 production.http://dx.doi.org/10.1080/09629350210309
collection DOAJ
language English
format Article
sources DOAJ
author Sergey V. Kalashnikov
Elena A. Kalashnikova
Svetlana N. Kokarovtseva
spellingShingle Sergey V. Kalashnikov
Elena A. Kalashnikova
Svetlana N. Kokarovtseva
Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro
Mediators of Inflammation
author_facet Sergey V. Kalashnikov
Elena A. Kalashnikova
Svetlana N. Kokarovtseva
author_sort Sergey V. Kalashnikov
title Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro
title_short Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro
title_full Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro
title_fullStr Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro
title_full_unstemmed Immunomodulating effects of tofizopam (Grandaxin®) and diazepam in vitro
title_sort immunomodulating effects of tofizopam (grandaxin®) and diazepam in vitro
publisher Hindawi Limited
series Mediators of Inflammation
issn 0962-9351
1466-1861
publishDate 2002-01-01
description Benzodiazepines (BDZs) are known to act not only in the central nervous system, but on peripheral cells and tissues binding to the peripheral-type benzodiazepine receptors. In the present study, the influence of two different BDZs (diazepam (Dz) and tofizopam (Tof)) on several immune functions has been examined in vitro. Some differences between Dz and Tof in their effects on human lymphocyte proliferative response, changes in glucocorticoid-induced suppression of cell proliferation and influence on cytokine production (tumor necrosis factor-α (TNF-α) and interleukin-2 (IL-2)) have been determined. Dz suppressed mitogen-induced peripheral blood mononuclear cell (PBMC) proliferation, enhanced dexamethasone-induced inhibition of PBMC proliferative response, and suppressed lymphocyte production of TNF-α and IL-2. Tof usually enhanced PBMC proliferation and IL-2 production in low and moderate doses, but in high doses it suppressed both. Tof in all investigated doses enhanced dexamethasone-induced suppression of lymphocyte proliferation and depressed TNF-α production. Thus, both Dz and Tof are shown to have immunomodulating effects in vitro. Tof, opposite to Dz even in the therapeutic doses, is able to enhance in vitro mitogen-induced lymphocyte proliferation and IL-2 production.
url http://dx.doi.org/10.1080/09629350210309
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