Anna Drzazga

Dr. Anna Drzazga


Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

View All Publications
1 September 2018 in Molecular and Cellular Endocrinology
Verified
Journal Article
Closed access
ADAnna Drzazga
Anna Drzazga
HKHjalti Kristinsson
Hjalti Kristinsson
Maciej SałagaMaciej Sałaga
Maciej Sałaga
HZHubert Zatorski
Hubert Zatorski
Maria KoziołkiewiczMaria Koziołkiewicz
Maria Koziołkiewicz
PBPeter Bergsten
Peter Bergsten

16 May 2020 in Antioxidants
Verified
Journal Article
Open access
MZMalgorzata Zakłos-Szyda
Malgorzata Zakłos-Szyda
AKAgnieszka Kowalska-Baron
Agnieszka Kowalska-Baron
Nina PietrzykNina Pietrzyk
Nina Pietrzyk
ADAnna Drzazga
Anna Drzazga
APAnna Podsedek
Anna Podsedek
In this study, the influence of guelder rose (Viburnum opulus) fruit fresh juice (FJ) and a phenolic-rich fraction (PRF) isolated from juice on mice insulinoma MIN6 cells activities was investigated. Extracts were able to decrease intracellular oxidative stress at the highest non-cytotoxic concentrations. They induced glucagon-like peptide-1 (GLP-1) secretion in the presence of an elevated glucose concentration, and they inhibited in vitro activity of the dipeptidyl peptidase-4 (DPP4) enzyme. Nonetheless, inhibition of glucose-stimulated insulin secretion was detected, which was accompanied by a decrease of cellular membrane fluidity and hyperpolarization effect. In addition, the increase of free fatty acid uptake and accumulation of lipid droplets in MIN6 cells were observed. Elevated extract concentrations induced cell apoptosis through the intrinsic mitochondrial pathway with activation of initiatory caspase-9 and downstream caspases-3/7. The fluorescence-quenching studies indicated that PRF extract has binding affinity to human serum albumin, which is one of the factors determining drug bioavailability. Taken together, despite the cytoprotective activity against generated intracellular oxidative stress, V. opulus revealed potential toxic effects as well as decreased insulin secretion from MIN6 cells. These findings are relevant in understanding V. opulus limitations in developing diet supplements designed for the prevention and treatment of postprandial glucose elevation.


1 July 2017 in Biochemical and Biophysical Research Communications
Verified
Journal Article
Closed access
ADAnna Drzazga
Anna Drzazga
ASAgata Sowinska
Agata Sowinska
Agnieszka KrzemińskaAgnieszka Krzemińska
Agnieszka Krzemińska
PRPrzemysław Rytczak
Przemysław Rytczak
Maria KoziołkiewiczMaria Koziołkiewicz
Maria Koziołkiewicz
EGEdyta Gendaszewska-Darmach
Edyta Gendaszewska-Darmach

1 October 2019 in Trends in Molecular Medicine
Verified
Journal Article
Closed access
EGEdyta Gendaszewska-Darmach
Edyta Gendaszewska-Darmach
ADAnna Drzazga
Anna Drzazga
MKMaria Koziołkiewicz
Maria Koziołkiewicz

22 April 2020 in Nutrients
Verified
Journal Article
Open access
PDF file
ADAnna Drzazga
Anna Drzazga
MCMarta Czarnecka
Marta Czarnecka
MRMagdalena Rychlicka
Magdalena Rychlicka
Łukasz BiegałaŁukasz Biegała
Łukasz Biegała
Anna GliszczyńskaAnna Gliszczyńska
Anna Gliszczyńska
EGEdyta Gendaszewska-Darmach
Edyta Gendaszewska-Darmach
Diabetes mellitus is a worldwide health problem with high rates of mortality and morbidity. Management of diabetes mellitus by dietary components is achievable especially at the initial stage of the disease. Several studies confirmed the antidiabetic activities of simple phenolic acids and lysophosphatidylcholine (LPC). The main goal of this study was to identify new potential insulin secretion modulators obtained by combining the structures of two natural compounds, namely O-methyl derivatives of phenolic acids and phospholipids. LPC and phosphatidylcholine bearing methoxylated aromatic carboxylic acids were tested as potential agents able to improve glucose-stimulated insulin secretion (GSIS) and intracellular calcium mobilization in MIN6 β pancreatic cell line. Our results show that LPC with covalently bonded molecule of p-anisic acid at the sn-1 position was able to induce GSIS and intracellular calcium flux. Notably, 1-anisoyl-2-hydroxy-sn-glycero-3-phosphocholine did not affect the viability of MIN6 cells, suggesting its potential safe use. Furthermore, we have shown that three G protein coupled receptors, namely GPR40, GPR55, and GPR119, are targeted by this LPC derivative.