2017
TLR-9 expression in dorsal root ganglia induced by Paclitaxel treatment
LEVIN, Shahaf, Kateřina KUBÍČKOVÁ, Ilona KLUSÁKOVÁ, Petr DUBOVÝ, Marek JOUKAL et. al.Základní údaje
Originální název
TLR-9 expression in dorsal root ganglia induced by Paclitaxel treatment
Autoři
Vydání
Morphology 2017, 2017
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
30000 3. Medical and Health Sciences
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Organizační jednotka
Lékařská fakulta
ISBN
978-80-263-1315-1
Změněno: 27. 9. 2017 12:35, MUDr. Shahaf Levin
Anotace
V originále
Chemotherapeutic agent Paclitaxel causes peripheral neuropathy based on alteration of calcium channels and defragmentation of mitochondria in peripheral nerve axons. These changes are related to the release of damage associated molecular patterns (DAMPs) which are associated with the expression of Toll-like receptor 9 (TLR-9). The aim of our study was to assess the changes of TLR-9 in the dorsal root ganglia (DRGs), related to Paclitaxel application. Wistar rats (n=18, males) were used in our experiments. Intraperitoneal injections of Paclitaxel in 4 doses with a cumulative dose of 8 mg/kg were performed on experimental rats, while control animals received vehiculum (alcohol and cremophor; 1:1). The animals were left to survive for 1, 3 and 7 days from the last application. Experimental and control rats were sacrificed together with naïve rats and perfused transcardially by Zamboni´s fixative. Longitudinal cryostat sections through the lumbar and cervical DRGs were cut and immunostained for TLR-9. Satellite glial cells (SGCs) were visualized using GFAP antibody. The intensity of TLR-9 immunofluorescence in the DRG was measured and statistically analyzed. The presence of TLR-9 immunofluorescence was found in the cytoplasm of both small-sized neurons and of satellite glial cells surrounding large-sized neurons, in both naïve and control animals. However, the application of Paclitaxel caused a visible presence of TLR-9 in medium-sized neurons as well. Statistically significant increase in TLR-9 immunofluorescence was found in the DRGs of Paclitaxel treated animals in comparison to control and naïve animals. The intensity of TLR-9 immunofluorescence increased with time of survival after the last application. Our results clearly indicate that DRGs react to Paclitaxel application with an increase of TLR-9 expression. These changes might be associated with inflammatory reaction in chemotherapy induced peripheral neuropathy.
Návaznosti
MUNI/A/0973/2016, interní kód MU |
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