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DSS colitis model : traps, tricks, and reporting recommendations
ID
Perše, Martina
(
Avtor
)
PDF - Predstavitvena datoteka,
prenos
(3,82 MB)
MD5: E251A8A5E3F9C09DB875983EF99045AE
URL - Izvorni URL, za dostop obiščite
https://www.mdpi.com/2227-9059/14/4/928
Galerija slik
Izvleček
The dextran sodium sulfate (DSS) colitis model is the most widely used experimental model of inflammatory bowel disease (IBD) due to its simplicity and versatility, with over 7000 PubMed entries in the last decade and an exponential rise in recent years. Since its initial description in 1985, DSS colitis has been extensively evaluated across species, most notably in mice and rats, and has yielded substantial insights into IBD pathogenesis. However, the model’s multifactorial nature poses a dual challenge: it offers an opportunity but complicates study design, interpretation, and translational relevance. This complexity is worsened by inconsistent reporting, which hampers reproducibility and comparability across studies. The broad use of the DSS-induced colitis model yields numerous insights about the model, which help better understand its complexity, characteristics and limitations. Although DSS colitis is induced locally, inflammation in the colon and gut barrier destruction may also affect other organs (such as the liver and brain) and their metabolism and molecular responses, which, in turn, may interfere with colitis-underlying mechanisms and drug response, and may influence the interpretation of results. These intrinsic (intra-experimental) characteristics of the DSS model are summarised in the paper (colitis, gut–brain axis, gut–liver axis). In addition, the DSS model is heavily influenced by numerous extrinsic (inter-experimental) factors (environmental, microbiological, genetic), which may further complicate the colitis model, the study outcomes, and data interpretation, and these are also discussed in the paper. As science advances and new data accumulate, understanding the intricate interplay among internal mechanisms, external factors, and technical variables becomes increasingly essential for the accurate interpretation of DSS outcomes. This review synthesises the complexity and interdependence of factors shaping the DSS model, emphasising the need for meticulous reporting and consideration of methodological nuances to enhance reproducibility, interpretation, and translational value in DSS colitis research. In addition, the review provides practical guidance through a “traps and tricks” subsection and checklist table designed to provide a framework and practical recommendations to better understand, apply, and interpret DSS model results in the context of broader systemic and methodological considerations.
Jezik:
Angleški jezik
Ključne besede:
DSS
,
colitis
,
visceral pain
,
gut-brain axis
,
gut-liver axis
,
reporting
,
genetic
,
gut microbiota
,
immune cells
,
cytokines
,
inflammation
,
behaviour
Vrsta gradiva:
Članek v reviji
Tipologija:
1.02 - Pregledni znanstveni članek
Organizacija:
MF - Medicinska fakulteta
Status publikacije:
Objavljeno
Različica publikacije:
Objavljena publikacija
Leto izida:
2026
Št. strani:
41 str.
Številčenje:
Vol. 14, no. 4, art. 928
PID:
20.500.12556/RUL-185629
UDK:
616:577.2
ISSN pri članku:
2227-9059
DOI:
10.3390/biomedicines14040928
COBISS.SI-ID:
276196611
Datum objave v RUL:
13.08.2026
Število ogledov:
15
Število prenosov:
4
Metapodatki:
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Objavi na:
Gradivo je del revije
Naslov:
Biomedicines
Skrajšan naslov:
Biomedicines
Založnik:
MDPI
ISSN:
2227-9059
COBISS.SI-ID:
523006745
Licence
Licenca:
CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:
http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:
To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.
Sekundarni jezik
Jezik:
Slovenski jezik
Ključne besede:
kolitis
,
visceralna bolečina
,
os črevesje-možgani
,
os črevesje-jetra
,
poročanje
,
genetika
,
črevesna mikrobiota
,
imunske celice
,
citokini
,
vnetje
,
vedenje
Projekti
Financer:
ARRS - Agencija za raziskovalno dejavnost Republike Slovenije
Številka projekta:
P3-0054
Naslov:
Patologija in molekularna genetika
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