Detailed Information on Publication Record
2017
Depot risperidone-induced adverse metabolic alterations in female rats
HORSKÁ, Kateřina, Jana RUDÁ, Michal KARPISEK, Radka OPATŘILOVÁ, Pavel SUCHÝ et. al.Basic information
Original name
Depot risperidone-induced adverse metabolic alterations in female rats
Authors
HORSKÁ, Kateřina (203 Czech Republic), Jana RUDÁ (203 Czech Republic, guarantor, belonging to the institution), Michal KARPISEK (203 Czech Republic), Radka OPATŘILOVÁ (203 Czech Republic), Pavel SUCHÝ (203 Czech Republic) and Hana KOTOLOVÁ (203 Czech Republic)
Edition
Journal of Psychopharmacology, London, SAGE Publications Ltd. 2017, 0269-8811
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30104 Pharmacology and pharmacy
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.738
RIV identification code
RIV/00216224:14110/17:00096183
Organization unit
Faculty of Medicine
UT WoS
000400179400009
Keywords in English
Adipokine; depot risperidone; leptin; lipid profile; Sprague-Dawley rats
Tags
Tags
International impact, Reviewed
Změněno: 14/1/2021 13:51, Ing. Marcela Sedlářová
Abstract
V originále
Atypical antipsychotics are associated with adverse metabolic effects including weight gain, increased adiposity, dyslipidaemia, alterations in glucose metabolism and insulin resistance. Increasing evidence suggests that metabolic dysregulation precedes weight gain development. The aim of this study was to evaluate alterations in adipokines, hormones and basic serum biochemical parameters induced by chronic treatment with depot risperidone at two doses (20 and 40 mg/kg) in female Sprague–Dawley rats. Dose-dependent metabolic alterations induced by risperidone after 6 weeks of treatment were revealed. Concomitant to weight gain and increased liver weight, an adverse lipid profile with an elevated triglyceride level was observed in the high exposure group, administered a 40 mg/kg dose repeatedly, while the low dose exposure group, administered a 20 mg/kg dose, developed weight gain without alterations in the lipid profile and adipokine levels. An initial peak in leptin serum level after the higher dose was observed in the absence of weight gain. This finding may indicate that the metabolic alterations observed in this study are not consequent to body weight gain. Taken together, these data may support the primary effects of atypical antipsychotics on peripheral tissues.
Links
ROZV/24/LF/2016, interní kód MU |
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