Malgorzata Zwolinska-Wcislo

Prof. Malgorzata Zwolinska-Wcislo

Department of Gastroenterology and Hepatology, Faculty of Medicine, Medical College, Jagiellonian University in Cracow
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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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5 January 2015 in Mediators of Inflammation
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Journal Article
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Jan BilskiJan Bilski
Jan Bilski
AMAgnieszka Mazur-Bialy
Agnieszka Mazur-Bialy
BBBartosz Brzozowski
Bartosz Brzozowski
Marcin MagierowskiMarcin Magierowski
Marcin Magierowski
KJKatarzyna Jasnos
Katarzyna Jasnos
Tomasz BrzozowskiTomasz Brzozowski
Tomasz Brzozowski
Although progress has been recently made in understanding of inflammatory bowel diseases (IBD), their etiology is unknown apart from several factors from adipose tissue and skeletal muscles such as cytokines, adipokines, and myokines were implicated in the pathogenesis of ulcerative colitis. We studied the effect high‐fat diet (HFD; cholesterol up to 70%), low‐fat diet (LFD; cholesterol up to 10%), and the normal diet (total fat up to 5%) in rats with TNBS colitis forced to treadmill running exercise (5 days/week) for 6 weeks. In nonexercising HFD rats, the area of colonic damage, colonic tissue weight, the plasma IL‐1β, TNF‐α, TWEAK, and leptin levels, and the expression of IL‐1β‐, TNF‐α‐, and Hif1α mRNAs were significantly increased and a significant fall in plasma adiponectin and irisin levels was observed as compared to LFD rats. In HFD animals, the exercise significantly accelerated the healing of colitis, raised the plasma levels of IL‐6 and irisin, downregulated the expression of IL‐1β, TNF‐α, and Hif1α, and significantly decreased the plasma IL‐1β, TNF α, TWEAK, and leptin levels. We conclude that HFD delays the healing of colitis in trained rats via decrease in CBF and plasma IL‐1β, TNF‐α, TWEAK, and leptin levels and the release of protective irisin.

13 October 2021 in Journal of Clinical Medicine
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OKOlga Kaczmarczyk
Olga Kaczmarczyk
ADAgnieszka Dąbek-Drobny
Agnieszka Dąbek-Drobny
Michal WozniakiewiczMichal Wozniakiewicz
Michal Wozniakiewicz
PPPaweł Paśko
Paweł Paśko
JDJustyna Dobrowolska-Iwanek
Justyna Dobrowolska-Iwanek
Malgorzata Zwolinska-WcisloMalgorzata Zwolinska-Wcislo
Malgorzata Zwolinska-Wcislo
Intestinal dysbiosis plays a crucial role in the development of inflammatory bowel disease (IBD), including Crohn’s disease (CD) and ulcerative colitis (UC). The importance of bacterial metabolites, such as short-chain fatty acids (SCFAs), succinic and lactic acids, as well as environmental factors that affect their production in the course of IBD, remains unclear. The aim of this study was to evaluate a profile of organic acids in the stool of CD and UC patients with different disease activity. We assessed a correlation between used medications, patient’s diet, and SCFA levels. A total of 35 adult patients were included in the study. We did not observe significant differences in the levels of organic acids between the CD and UC groups, irrespective of disease activity, and a control group. However, propionic acid levels were higher in IBD patients who received trimebutine vs. those who did not (p = 0.031). Higher isobutyric acid levels were observed in patients treated with biological drugs compared with those without such treatment (p = 0.014). No significant correlations were found between organic acid levels and the frequency of dietary fiber consumption. Our results reveal a new link between medication use and organic acid levels in patients with IBD.

8 April 2013 in BMC Gastroenterology
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MPMagdalena Pilarczyk-Zurek
Magdalena Pilarczyk-Zurek
ACAgnieszka Chmielarczyk
Agnieszka Chmielarczyk
Tomasz GosiewskiTomasz Gosiewski
Tomasz Gosiewski
ATAnna Tomusiak
Anna Tomusiak
PAPaweł Adamski
Paweł Adamski
MSMagdalena Strus
Magdalena Strus
Background: This study investigated a possible role of Escherichia coli in propagation and perpetuation of the chronic inflammation in ulcerative colitis (UC). The lesions of UC are located superficially on the rectal and/or colonic mucosa. It is suggested that the commensal bacteria of the digestive tract may play a role in the pathogenesis of UC. Several studies have demonstrated proliferation of E. coli in the gut of UC patients. An increase in the number of E. coli in the inflamed tissue is most probably related to the abundance of iron ions produced by the bacteria. Methods: Colon mucosal biopsies were collected from 30 patients with acute-phase UC, both from tissues with inflammatory changes (n = 30) and unchanged tissue with no inflammatory changes (n = 30) from the same patient. Biopsies were also taken from 16 patients with irritable bowel syndrome diarrhea who comprised the control group. Quantitative and qualitative analysis of the biopsy specimens was performed using culture methods and real-time polymerase chain reaction (PCR). Genotyping of the E. coli isolates was done using pulsed-field gel electrophoresis. Multiplex PCR was used to compare the E. coli strains for the presence of genes responsible for synthesis of iron acquisition proteins: iroN, iutA, iha, ireA, chuA, and hlyA. Results: We demonstrated that there was a significant increase in the number of E. coli at the sites of inflammation in patients with UC compared to the control group (P = 0.031). Comparative analysis of the restriction patterns of E. coli isolated from inflammatory and unchanged tissues showed that the local inflammatory changes did not promote specific E. coli strains. There was a significant difference in the frequency of the iroN gene in E. coli isolated from patients with UC as compared to the control group. Conclusions: The increase in the numbers of E. coli in the inflammatory tissues is related to the presence of chuA and iutA genes, which facilitate iron acquisition during chronic intestinal inflammatory processes.

10 January 2022 in Biology
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Journal Article
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ADAgnieszka Dąbek-Drobny
Agnieszka Dąbek-Drobny
OKOlga Kaczmarczyk
Olga Kaczmarczyk
Michal WozniakiewiczMichal Wozniakiewicz
Michal Wozniakiewicz
PPPaweł Paśko
Paweł Paśko
JDJustyna Dobrowolska-Iwanek
Justyna Dobrowolska-Iwanek
Malgorzata Zwolinska-WcisloMalgorzata Zwolinska-Wcislo
Malgorzata Zwolinska-Wcislo
Disturbances in the production of bacterial metabolites in the intestine have been reported in diseases associated with dysbiosis, such as inflammatory bowel diseases (IBDs) that include two conditions: Crohn disease (CD) and ulcerative colitis (UC). Short-chain fatty acids (SCFAs) are the main dietary-fiber-derived bacterial metabolites associated with the course of intestinal inflammation. In this study, we assessed the relationship between body mass index (BMI), the type of diet used, and changes in fecal SCFA levels in patients with IBD. We performed nutritional assessments using a nutritional questionnaire and determined fecal SCFA levels in 43 patients with UC, 18 patients with CD, and 16 controls. Our results revealed that subjects with a BMI > 24.99 kg/m2 had higher levels of isobutyric acid, whereas those with a BMI < 18.5 kg/m2 had lower level of butyric, isovaleric, and propionic acids. Furthermore, we observed higher levels of valeric acid in controls than in IBD patients. We did not reveal a relationship between a specific SCFA and the type of diet, but eating habits appear to be related to the observed changes in the SCFA profile depending on BMI. In conclusion, we demonstrated that BMI is associated with SCFA levels in patients with IBD.

1 October 2010
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Journal Article
Closed access
DTDanuta Trojanowska
Danuta Trojanowska
Malgorzata Zwolinska-WcisloMalgorzata Zwolinska-Wcislo
Malgorzata Zwolinska-Wcislo
MTMarianna Tokarczyk
Marianna Tokarczyk
KKKrzysztof Kosowski
Krzysztof Kosowski
TMTomasz Mach
Tomasz Mach
ABAlicja Budak
Alicja Budak

2 November 2022 in Nutrients
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Journal Article
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OKOlga Kaczmarczyk
Olga Kaczmarczyk
ADAgnieszka Dąbek-Drobny
Agnieszka Dąbek-Drobny
APAgnieszka Piątek-Guziewicz
Agnieszka Piątek-Guziewicz
Michal WozniakiewiczMichal Wozniakiewicz
Michal Wozniakiewicz
PPPaweł Paśko
Paweł Paśko
Malgorzata Zwolinska-WcisloMalgorzata Zwolinska-Wcislo
Malgorzata Zwolinska-Wcislo
Intestinal inflammation in inflammatory bowel disease (IBD) is closely linked to nutrition. This study aimed to evaluate associations between nutritional, inflammatory, and intestinal barrier parameters in patients with IBD. We assessed nutritional status, fecal short-chain fatty acid profile, serum cytokine levels, and mRNA expression of enzymes and tight junction proteins in intestinal biopsies obtained from 35 patients, including 11 patients with inactive IBD, 18 patients with active IBD, and six controls. Patients with active IBD were characterized by hypoalbuminemia, fluctuations in body weight, and restriction of fiber-containing foods. In addition, they had significantly reduced levels of isovaleric acid and tended to have lower levels of butyric, acetic, and propionic acids. Patients with active IBD had higher mRNA expression of peroxisome proliferator-activated receptor γ and inducible nitric oxide synthase, and lower mRNA expression of claudin-2 and zonula occludens-1, compared with patients with inactive IBD. Moreover, patients with a body mass index (BMI) of ≥25 kg/m2 had higher median tumor necrosis factor-α levels that those with a lower BMI. We comprehensively evaluated inflammatory parameters in relation to IBD activity and nutritional status. The discrepancies between proinflammatory and anti-inflammatory parameters depending on IBD activity may be related to nutritional factors, including diet and abnormal body weight.