Publication: Therapeutic effects of an azaphenothiazine derivative in mouse experimental colitis
Authors
Artym, Jolanta ; Kocięba, Maja ; Zaczyńska, Ewa ; Zimecki, Michał ; Kałas, Wojciech ; Strządała, Leon ; Pawlak, Alicja ; Jeleń, Małgorzata ; Morak Młodawska, Beata ; Pluta, Krystian ; Kaleta Kuratewicz, Katarzyna ; Madej, Jan P. ; Kuropka, Piotr ; Kuryszko, Jan
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Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
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DOI
https://doi.org/10.14670/HH-18-192
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info:eu-repo/semantics/article
Description
Abstract
Phenothiazines represent a class of
compounds of potential therapeutic utility. In this report
we evaluated therapeutic value of an azaphenothiazine
derivative, 6-acetylaminobutyl-9-chloroquino[3,2-
b]benzo[1,4]thiazine (QBT), given intragastrically, in the
model of dextran sodium sulfate-induced colitis in
C57BL/6 mice using 5-aminosalicylic acid (5-ASA) as a
reference drug. Colitis symptoms such as body weight
loss, diarrhea and hematochezia (blood in stool) were
observed and registered and disease activity index (DAI)
was calculated. In addition, weight and cell numbers in
the lymphatic organs and histological parameters of the
colon wall were analyzed. The effects of QBT on
viability of colon epithelial cell lines were also
determined. We showed that weight and cell number of
draining mesenteric lymph nodes were lower in mice
treated with QBT in comparison to their control
counterparts. The number of thymocytes, drastically
reduced in control mice, was elevated in mice treated
with the compounds with a significant effect of 5-ASA.
In addition, an abnormal composition of blood cell types
was partially corrected in these groups. Histological
analysis of the colon revealed that the pathological
changes were partially normalized by QBT and even to a
higher degree by 5-ASA. In conclusion we demonstrated
a therapeutic efficacy of the compound in amelioration
of local and systemic pathological changes associated
with chemically-induced colitis in mice. A possible
mechanism of action of the compound is discussed.
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Citation
Histology and Histopathology Vol. 35, nº7 (2020)
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