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https://hdl.handle.net/11499/8264
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yüksel, Aykut | - |
dc.contributor.author | Erdur, Bülent | - |
dc.contributor.author | Kortunay, Selim | - |
dc.contributor.author | Ergin, Ahmet | - |
dc.date.accessioned | 2019-08-16T12:37:48Z | |
dc.date.available | 2019-08-16T12:37:48Z | |
dc.date.issued | 2013 | - |
dc.identifier.issn | 1382-6689 | - |
dc.identifier.uri | https://hdl.handle.net/11499/8264 | - |
dc.identifier.uri | https://doi.org/10.1016/j.etap.2012.11.001 | - |
dc.description.abstract | Study objective: To evaluate the effects of pretreatment, midazolam (M), propofol (P), ziprasidone (Z), and two combinations of [(midazolam plus propofol (MP); midazolam plus ziprasidone (MZ)] in mice models in the prevention of seizures, and death due to acute cocaine toxicity. Methods: 180 male CF-1 mice were randomized to 6 groups (30/group) in this experimental study. The animals were administered intraperitoneal injections of M (2. mg/kg), P (25. mg/kg), Z (4. mg/kg), MP (2. mg/kg and 25. mg/kg) and MZ (2. mg/kg and 4. mg/kg) or saline (S) as a pretreatment 10. min later, the mice were administered intraperitoneal injections of 105. mg/kg cocaine. The groups were observed for cocaine-induced seizure and lethality. Results: The MP and MZ combinations showed the highest protective effect in terms of seizure and lethality relative to P and S (p< 0.001). M and Z were found effective compared to P and S (p< 0.001). There were no significant differences among MP and MZ, however there were significant differences between MP and Z in terms of lethality (p= 0.05). There were no significant differences among MP, MZ, M and Z groups in terms of seizure (p>. 0.05). No death was observed in the MP combination group. Seizure rate was observed o be least in the MZ group with respect to the other groups. Conclusion: According to our particular mouse model, this study suggests that MP and MZ combinations may be more effective than M or Z only for the prevention of cocaine-induced seizure and lethality. However, P alone does not prevent cocaine-induced seizure and lethality. © 2012 Elsevier B.V. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Environmental Toxicology and Pharmacology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Cocaine intoxication | en_US |
dc.subject | Midazolam | en_US |
dc.subject | New generation antipsychotic | en_US |
dc.subject | Propofol | en_US |
dc.subject | Ziprasidone | en_US |
dc.subject | midazolam | en_US |
dc.subject | propofol | en_US |
dc.subject | ziprasidone | en_US |
dc.subject | acute toxicity | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | article | en_US |
dc.subject | cocaine toxicity | en_US |
dc.subject | combination chemotherapy | en_US |
dc.subject | controlled study | en_US |
dc.subject | drug efficacy | en_US |
dc.subject | lethality | en_US |
dc.subject | male | en_US |
dc.subject | mortality | en_US |
dc.subject | nonhuman | en_US |
dc.subject | priority journal | en_US |
dc.subject | randomized controlled trial | en_US |
dc.subject | seizure | en_US |
dc.subject | Animals | en_US |
dc.subject | Anticonvulsants | en_US |
dc.subject | Antipsychotic Agents | en_US |
dc.subject | Cocaine-Related Disorders | en_US |
dc.subject | Disease Models, Animal | en_US |
dc.subject | Dopamine Antagonists | en_US |
dc.subject | Drug Therapy, Combination | en_US |
dc.subject | GABA Modulators | en_US |
dc.subject | Male | en_US |
dc.subject | Mice | en_US |
dc.subject | Piperazines | en_US |
dc.subject | Seizures | en_US |
dc.subject | Serotonin Antagonists | en_US |
dc.subject | Thiazoles | en_US |
dc.subject | Animalia | en_US |
dc.subject | Mus | en_US |
dc.title | Assessment of propofol, midazolam and ziprasidone, or the combinations for the prevention of acute cocaine toxicity in a mouse model | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 35 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 61 | |
dc.identifier.startpage | 61 | en_US |
dc.identifier.endpage | 66 | en_US |
dc.identifier.doi | 10.1016/j.etap.2012.11.001 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 23257283 | en_US |
dc.identifier.scopus | 2-s2.0-84871250629 | en_US |
dc.identifier.wos | WOS:000314262300008 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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