Multiple impairments of cutaneous nociceptor function induced by cardiotoxic doses of Adriamycin in the rat

Besides their deleterious action on cardiac muscle, anthracycline-type cytostatic agents exert significant neurotoxic effects on primary sensory neurons. Since cardiac sensory nerves confer protective effects on heart muscle and share common traits with cutaneous chemosensitive nerves, this study ex...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Boros Krisztina
Jancsó Gábor
Dux Mária
Fekécs Zoltán
Bencsik Péter
Oszlács Orsolya
Jancsó Gáborné Katona Márta
Ferdinandy Péter
Nógrádi Antal
Sántha Péter
Dokumentumtípus: Cikk
Megjelent: Springer-Verlag 2016
Sorozat:NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY 389 No. 9
doi:10.1007/s00210-016-1267-x

mtmt:3088769
Online Access:http://publicatio.bibl.u-szeged.hu/11152
LEADER 02986nab a2200313 i 4500
001 publ11152
005 20191129143311.0
008 170411s2016 hu o 0|| zxx d
022 |a 0028-1298 
024 7 |a 10.1007/s00210-016-1267-x  |2 doi 
024 7 |a 3088769  |2 mtmt 
040 |a SZTE Publicatio Repozitórium  |b hun 
041 |a zxx 
100 1 |a Boros Krisztina 
245 1 0 |a Multiple impairments of cutaneous nociceptor function induced by cardiotoxic doses of Adriamycin in the rat  |h [elektronikus dokumentum] /  |c  Boros Krisztina 
260 |a Springer-Verlag  |c 2016 
300 |a 1009-1020 
490 0 |a NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY  |v 389 No. 9 
520 3 |a Besides their deleterious action on cardiac muscle, anthracycline-type cytostatic agents exert significant neurotoxic effects on primary sensory neurons. Since cardiac sensory nerves confer protective effects on heart muscle and share common traits with cutaneous chemosensitive nerves, this study examined the effects of cardiotoxic doses of adriamycin on the function and morphology of epidermal nerves. Sensory neurogenic vasodilatation, plasma extravasation, and the neural CGRP release evoked by TRPV1 and TRPA1 agonists in vitro were examined by using laser Doppler flowmetry, the Evans blue technique, and ELISA, respectively. Carrageenan-induced hyperalgesia was assessed with the Hargreaves method. Immunohistochemistry was utilized to study cutaneous innervation. Adriamycin treatment resulted in profound reductions in the cutaneous neurogenic sensory vasodilatation and plasma extravasation evoked by the TRPV1 and TRPA1 agonists capsaicin and mustard oil, respectively. The in vitro capsaicin-, but not high potassium-evoked neural release of the major sensory neuropeptide, CGRP, was markedly attenuated after adriamycin treatment. Carrageenan-induced inflammatory hyperalgesia was largely abolished following the administration of adriamycin. Immunohistochemistry revealed a substantial loss of epidermal TRPV1-expressing nociceptive nerves and a marked thinning of the epidermis. These findings indicate impairments in the functions of TRPV1 and TRPA1 receptors expressed on cutaneous chemosensitive nociceptive nerves and the loss of epidermal axons following the administration of cardiotoxic doses of adriamycin. Monitoring of the cutaneous nociceptor function in the course of adriamycin therapy may well be of predictive value for early detection of the deterioration of cardiac nerves which confer protection against the deleterious effects of the drug. 
700 0 1 |a Jancsó Gábor  |e aut 
700 0 1 |a Dux Mária  |e aut 
700 0 1 |a Fekécs Zoltán  |e aut 
700 0 1 |a Bencsik Péter  |e aut 
700 0 1 |a Oszlács Orsolya  |e aut 
700 0 2 |a Jancsó Gáborné Katona Márta  |e aut 
700 0 2 |a Ferdinandy Péter  |e aut 
700 0 2 |a Nógrádi Antal  |e aut 
700 0 2 |a Sántha Péter  |e aut 
856 4 0 |u http://publicatio.bibl.u-szeged.hu/11152/1/BorosK_NSArchP_2016.pdf  |z Dokumentum-elérés