Jana Drapalova
Charles University in Prague
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Featured researches published by Jana Drapalova.
Obesity | 2013
Denisa Haluzikova; Lacinová Z; Petra Kaválková; Jana Drapalova; Jarmila Křížová; Marketa Bartlova; Miloš Mráz; T. Petr; Libor Vitek; Mojmír Kasalický; Martin Haluzik
Fibroblast growth factor (FGF)‐19 and FGF‐21 are novel metabolic regulators that improve insulin resistance and obesity in rodents. The aim of the study was to assess the effects of laparoscopic sleeve gastrectomy (LSG) on serum concentrations of FGF‐19 and FGF‐21 along with circulating bile acids and other relevant hormonal and biochemical parameters.
The Journal of Clinical Endocrinology and Metabolism | 2011
Miloš Mráz; Zdena Lacinova; Jana Drapalova; Denisa Haluzikova; A. Horinek; Martin Matoulek; Pavel Trachta; Petra Kaválková; Štěpán Svačina; Martin Haluzik
CONTEXTnLow-grade inflammation links obesity, type 2 diabetes mellitus (T2DM), and cardiovascular diseases.nnnOBJECTIVEnTo explore the expression profile of genes involved in inflammatory pathways in adipose tissue and peripheral monocytes (PM) of obese patients with and without T2DM at baseline and after dietary intervention.nnnDESIGNnTwo-week intervention study with very-low-calorie diet (VLCD).nnnSETTINGnUniversity hospital.nnnPATIENTSnTwelve obese females with T2DM, 8 obese nondiabetic females (OB) and 15 healthy age-matched females.nnnINTERVENTIONnTwo weeks of VLCD (2500 kJ/d).nnnMAIN OUTCOME MEASURESnMetabolic parameters, circulating cytokines, hormones, and mRNA expression of 39 genes in sc adipose tissue (SCAT) and PM.nnnRESULTSnBoth T2DM and OB group had significantly increased serum concentrations of circulating proinflammatory factors (C-reactive protein, TNFα, IL-6, IL-8), mRNA expression of macrophage antigen CD68 and proinflammatory chemokines (CCL-2, -3, -7, -8, -17, -22) in SCAT and complementary chemokine receptors (CCR-1, -2, -3, -5) and other proinflammatory receptors (toll-like receptor 2 and 4, TNF receptor superfamily 1A and 1B, IL-6R) in PM, with OB group showing less pronounced chemoattracting and proinflammatory profile compared to T2DM group. In T2DM patients VLCD decreased body weight, improved metabolic profile, and decreased mRNA expression of up-regulated CCRs in PM and chemokines [CCL 8, chemokine (C-X-C motif) ligand 10] in SCAT. VLCD markedly increased mRNA expression of T-lymphocyte attracting chemokine CCL-17 in SCAT.nnnCONCLUSIONnObese patients with and without T2DM have increased mRNA expression of chemotactic and proinflammatory factors in SCAT and expression of corresponding receptors in PM. Two weeks of VLCD significantly improved this profile in T2DM patients.
Haematologica | 2013
Zdenek Racil; Filip Rázga; Jana Drapalova; Lucie Burešová; Daniela Zackova; Martina Palacková; Lukáš Semerád; Ludmila Malásková; Martin Haluzik; Jiri Mayer
Hyperglycemia represents frequent adverse event reported in chronic myelogenous leukemia (CML) patients treated with nilotinib. In order to determine the major mechanism of glucose metabolism impairment, we performed a metabolic analysis using an oral glucose tolerance test as well as assessment of incretins and adipokines at baseline and after 3 months of nilotinib treatment in patients with CML. We proved that rapid insulin resistance, compensatory hyperinsulinaemia, and hypoadiponectinaemia develop after initiation of nilotinib therapy, which clarifies not only the mechanism of impaired glucose metabolism, but also explains the fast development of dyslipidaemia and peripheral artery occlusion in nilotinib-treated CML patients.
International Journal of Obesity | 2013
José María Moreno-Navarrete; V. Touskova; Mònica Sabater; Miloš Mráz; Jana Drapalova; F Ortega; Marta Serrano; Victoria Catalán; Javier Gómez-Ambrosi; M R Ortiz; Gerard Pardo; Neus Pueyo; W Ricart; Lacinová Z; Martin Haluzik; Gema Frühbeck; José Manuel Fernández-Real
Objective:Recent studies linked circulating pigment epithelium-derived factor (PEDF) to obesity-associated insulin resistance, but the main source of circulating PEDF is unknown. We aimed to investigate liver and adipose tissue PEDF gene expression in association with obesity and insulin resistance.Design, subjects and methods:Three (two cross-sectional and one longitudinal) independent cohorts have been studied, for adipose tissue (n=80 and n=30) and liver gene expression (n=32 and n=14). Effects of high glucose and cytokines on HepG2 cell line were also investigated. PEDF gene expression and circulating PEDF were analyzed using real-time PCR and ELISA, respectively.Results:In a first cohort of subjects, PEDF relative gene expression was higher in subcutaneous (SC) than in omental (OM) adipose tissue (P<0.0001) being also higher in mature adipocytes compared with stromo-vascular cells (P<0.0001). However, OM PEDF relative gene expression was decreased in morbidly obese subjects (P=0.01). Both OM PEDF and OM PEDF receptor (PEDFR) correlated positively with lipogenic and lipolytic genes, and with genes implicated in the lipid vacuole formation. Circulating PEDF levels were not associated with fat PEDF gene expression. In the second cohort, SC PEDF was decreased in subjects with type 2 diabetes and did not change significantly after weight loss. We next explored circulating PEDF in association with markers of liver-related insulin resistance injury (alanine aminotransferase, r=0.59, P=0.001). Interestingly, liver PEDF gene expression increased with obesity and insulin resistance in men, being significantly associated with fasting glucose and glycated hemoglobin in two independent cohorts. In fact, high glucose led to increased PEDF in HepG2 cells, while inflammatory stimuli present in the adipose tissue environment downregulated PEDF.Conclusion:Liver, but not adipose tissue, might be the source of increased circulating PEDF linked to insulin resistance.
Molecular and Cellular Endocrinology | 2014
Pavel Trachta; Ivana Dostálová; Denisa Haluzikova; M. Kasalický; Petra Kaválková; Jana Drapalova; M. Urbanová; Lacinová Z; Miloš Mráz; Martin Haluzik
Low-grade inflammation links obesity, insulin resistance, and cardiovascular diseases. We investigated the effects of laparoscopic sleeve gastrectomy (LSG) on expression profile of genes involved in inflammatory pathways in subcutaneous adipose tissue (SCAT) and peripheral monocytes (PM). At baseline, obese group had significantly increased mRNA expression of proinflammatory chemokines (CCL-3, -17, -22), chemokine receptor CCR1 and cytokines (IL-10, IL-18) in SCAT and chemokine and other proinflammatory receptors (CCR-1, -2, -3, TLR-2, -4) in PM relative to control group. LSG decreased body weight, improved metabolic profile and reduced mRNA expression of up-regulated chemokine receptors, chemokines and cytokines in SCAT. In contrast, expression profiles in PM were largely unaffected by LSG. We conclude that LSG improved proinflammatory profile in subcutaneous fat but not in peripheral monocytes. The sustained proinflammatory and chemotactic profile in PM even 2 years after LSG may contribute to partial persistence of metabolic complications in obese patients after metabolic surgery.
Cryobiology | 2014
Jana Drapalova; Petr Kopecky; Marketa Bartlova; Zdena Lacinova; Daniel Novák; Pavel Maruna; Michal Lips; Miloš Mráz; Jaroslav Lindner; Martin Haluzik
Changes in endocrine function of adipose tissue during surgery, such as excessive production of proinflammatory cytokines, can significantly alter metabolic response to surgery and worsen its outcomes and prognosis of patients. Therapeutic hypothermia has been used to prevent damage connected with perioperative ischemia and hypoperfusion. The aim of our study was to explore the influence of deep hypothermia on systemic and local inflammation, adipose tissue hypoxia and adipocytokine production. We compared serum concentrations of proinflammatory markers (CRP, IL-6, IL-8, sIL-2R, sTNFRI, PCT) and mRNA expression of selected genes involved in inflammatory reactions (IL-6, TNF-α, MCP-1, MIF) and adaptation to hypoxia and oxidative stress (HIF1-α, MT3, GLUT1, IRS1, GPX1, BCL-2) in subcutaneous and visceral adipose tissue and in isolated adipocytes of patients undergoing cardiosurgical operation with hypothermic period. Deep hypothermia significantly delayed the onset of surgery-related systemic inflammatory response. The relative gene expression of the studied genes was not altered during the hypothermic period, but was significantly changed in six out of ten studied genes (IL-6, MCP-1, TNF-α, HIF1-α, GLUT1, GPX1) at the end of surgery. Our results show that deep hypothermia suppresses the development of systemic inflammatory response, delays the onset of local adipose tissue inflammation and thus may protect against excessive expression of proinflammatory and hypoxia-related factors in patients undergoing elective cardiac surgery procedure.
Physiological Research | 2011
Miloš Mráz; Lacinová Z; Petra Kaválková; Denisa Haluzikova; Pavel Trachta; Jana Drapalova; Hanušová; Martin Haluzik
Physiological Research | 2014
M. Urbanová; Ivana Dostálová; Pavel Trachta; Jana Drapalova; Petra Kaválková; Denisa Haluzikova; Martin Matoulek; Lacinová Z; Miloš Mráz; Mojmír Kasalický; Martin Haluzik
Physiological Research | 2011
Tomas Kotulak; Jana Drapalova; Petr Kopecký; Zdena Lacinova; Kramář P; Říha H; Ivan Netuka; Malý J; Daniel Housa; Jan Bláha; Štěpán Svačina; Martin Haluzik
Physiological Research | 2014
Pavel Trachta; Jana Drapalova; Petra Kaválková; Toušková; Anna Cinkajzlova; Lacinová Z; Martin Matoulek; Tomas Zelinka; Widimský J; Miloš Mráz; Martin Haluzik