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Details

Autor(en) / Beteiligte
Titel
Antiplatelet agents’-ticagrelol and eptifibatide-safety in experimental colitis in mice
Ist Teil von
  • The Turkish Journal of Gastroenterology, 2020-06, Vol.31 (6), p.451-458
Ort / Verlag
AVES
Erscheinungsjahr
2020
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
  • Background/Aims: To evaluate the side effects of two antiplatelet agents--ticagrelor and eptifibatide - in mice with experimentally-induced inflammatory bowel disease. Materials and Methods: This study was designed as a controlled, animal, drug safety investigation. C57Bl/6 mice were used to establish the ulcerative colitis model by exposure to dextran sulfate sodium (DSS) and divided into three experimental groups: eptifibatide treated (150 [micro]g/day intraperitoneally; n=10), ticagrelor treated (1 mg/day via gastric tube; n=10), and DSS control (plain drinking water; n=10). An unmodeled non-DSS group served as the experimental control. Complete blood count was taken for all mice at baseline (day 0, treatment initiation) and after four days of treatment. On day 4, all animals were sacrificed for autopsy. The primary outcome measure was bleeding, and the secondary outcomes were changes in platelet count, hemoglobin level, and hematocrit level. Results: Neither ticagrelor nor eptifibatide treatment produced a significant effect on DSS colitis mice for the safety parameters measured. Platelet count and hemoglobin and hematocrit levels were statistically similar between the three DSS groups and the non-DSS control group (p>0.05). Autopsy found no evidence of recent bleeding in liver, spleen, central nervous system, or serous cavities. Conclusion: The antiplatelet agents, ticagrelor and eptifibatide, were safe in DSS colitis mice, suggesting their potential in humans suffering from ulcerative colitis and supporting future safety studies. Keywords: Dextran sulfate, colitis, ticagrelor, eptifibatide, mice, adverse effects
Sprache
Englisch
Identifikatoren
ISSN: 2148-5607, 1300-4948
eISSN: 2148-5607
DOI: 10.5152/tjg.2020.19454
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7433996

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