Barbara Malinowska

ORCID: 0000-0002-7057-8153
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About
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Research Areas
  • Cannabis and Cannabinoid Research
  • Receptor Mechanisms and Signaling
  • Neuroscience of respiration and sleep
  • Diet, Metabolism, and Disease
  • Neurotransmitter Receptor Influence on Behavior
  • Nitric Oxide and Endothelin Effects
  • Eicosanoids and Hypertension Pharmacology
  • Alcohol Consumption and Health Effects
  • Mast cells and histamine
  • Neuropeptides and Animal Physiology
  • Neuroscience and Neuropharmacology Research
  • Sleep and Wakefulness Research
  • Nicotinic Acetylcholine Receptors Study
  • Neuroendocrine regulation and behavior
  • Pharmacological Effects and Assays
  • Olfactory and Sensory Function Studies
  • Circadian rhythm and melatonin
  • Pulmonary Hypertension Research and Treatments
  • Adipose Tissue and Metabolism
  • Heart Rate Variability and Autonomic Control
  • Hormonal Regulation and Hypertension
  • Cardiac Ischemia and Reperfusion
  • Forensic Toxicology and Drug Analysis
  • Diet and metabolism studies
  • Tuberculosis Research and Epidemiology

Medical University of Białystok
2016-2025

King's College London
2016

Centro Cardiologico Monzino
2016

Institute of Experimental Cardiology
2016

Imperial College London
2016

University of Florence
2016

University of Bonn
1991-2012

Wrocław University of Science and Technology
2012

October 6 University
1997

Universitat de les Illes Balears
1996

We investigated the influence of cannabidiol (CBD) on blood pressure (BP) and heart rate (HR) in spontaneously (SHR) deoxycorticosterone (DOCA-salt) hypertensive rats. Hypertension was connected with increases cardiac plasma markers lipid peroxidation both models, whereas endocannabinoid levels decreased SHR increased DOCA-salt. CBD (10 mg/kg once a day for 2 weeks) did not modify BP HR hypertension but counteracted pro-oxidant effects. Moreover, it or anandamide, 2-arachidonoylglycerol...

10.3390/ijms21041295 article EN International Journal of Molecular Sciences 2020-02-14

Objective: Cannabidiol (CBD) has been suggested as a potential antihypertensive drug. The aim of our study was to investigate its vasodilatory effect in isolated human pulmonary arteries (hPAs) and rat small mesenteric (sMAs). Methods: Vascular effects CBD were examined hPAs obtained from patients during resection lung carcinoma sMAs spontaneously hypertensive (SHR); 11-deoxycorticosterone acetate (DOCA-salt) rats or their appropriate normotensive controls using organ bath wire myography,...

10.1097/hjh.0000000000002333 article EN Journal of Hypertension 2019-12-04

Cannabidiol (CBD) is known for its vasorelaxant (including in the human pulmonary artery), anti-proliferative and anti-inflammatory properties. The aim of our study was to examine potential preventive effect chronic CBD administration (10 mg/kg/day three weeks) on monocrotaline (MCT)-induced hypertension (PH) rats. PH connected with elevation right ventricular systolic pressure; ventricle hypertrophy; lung edema; artery remodeling; enhancement vasoconstrictor decreasing vasodilatory...

10.3390/ijms21197077 article EN International Journal of Molecular Sciences 2020-09-25

Pulmonary hypertension (PH) is a progressive disease characterized by elevated blood pressure in the pulmonary arteries, associated also with inflammation and oxidative stress. Inducible nitric oxide synthase (iNOS) one of key mediators immune system activation. Although preclinical studies mostly suggest detrimental role iNOS overactivation PH, there lack exhaustive analyses summaries. Therefore, this literature overview aims to fill gap. The involvement pathogenesis four main clinical...

10.3390/antiox14040377 article EN cc-by Antioxidants 2025-03-21

The influence of β 1 , 2 and 3 ‐adrenoceptor agonists CGP 12177 cyanopindolol on heart rate diastolic blood pressure was studied in the pithed rat. agonist, prenalterol, increased fenoterol, caused a fall pressure. effect prenalterol antagonized by antagonist, 20712 0.1 μ m ol kg −1 action fenoterol attenuated ICI 118551 . Both effects were markedly diminished non‐selective β‐adrenoceptor bupranolol isoprenaline, three ‐agonists as well elicited positive chronotropic effect, exhibiting...

10.1111/j.1476-5381.1996.tb15285.x article EN British Journal of Pharmacology 1996-03-01

Cannabidiol (CBD) is a nonpsychotropic constituent of Cannabis sativa L. It suggested to be useful in hypertension. Under vitro conditions, it activates vanilloid TRPV1 and inhibits serotonin 5-HT3 receptors, i.e., receptors involved the Bezold-Jarisch reflex stimulation. The aim our study was compare cardiovascular effects CBD spontaneously hypertensive (SHR) normotensive Wistar Kyoto (WKY) rats. Experiments were performed on conscious, urethane-anesthetized, pithed In SHR WKY, increased...

10.3389/fphar.2019.00500 article EN cc-by Frontiers in Pharmacology 2019-05-22

Background The endocannabinoid anandamide is implicated in the pathogenesis of hypotension haemorrhagic, endotoxic, and cardiogenic shock. It has been demonstrated animal, but not human, vessels that vasodilatory effects abnormal cannabidiol are partially mediated by an as yet unidentified endothelial cannabinoid receptor. Our study was performed to examine influence on human pulmonary artery. Methods Isolated arteries were obtained from patients without clinical evidence hypertension during...

10.1097/hjh.0b013e3282ef7a0a article EN Journal of Hypertension 2007-11-01

The endocannabinoid virodhamine is a partial agonist at the cannabinoid CB(1) receptor and full CB(2) receptor, relaxes rat mesenteric arteries through endothelial receptors. Its concentration in periphery exceeds that of anandamide. Here, we examined influence on human pulmonary artery.Isolated were obtained during resections for lung carcinoma. Vasorelaxant effects endothelium-intact vessels precontracted with 5-HT or KCl.Virodhamine, unlike WIN 55,212-2, relaxed 5-HT-precontracted...

10.1038/bjp.2008.371 article EN British Journal of Pharmacology 2008-09-22

Recent evidence suggests that endocannabinoids acting via cannabinoid CB 1 receptors may modulate vascular responses of various vasoconstrictors in the rodent systemic vasculature. The aim study was to investigate whether contractile evoked by a thromboxane A 2 analog (U46619), angiotensin II (ANG II), serotonin (5-HT), and phenylephrine, which stimulate distinct G q/11 protein-coupled (thromboxane, ANG type 1, 5-HT , α -adrenergic receptors) isolated endothelium-intact human rat pulmonary...

10.1152/ajpregu.00324.2016 article EN AJP Regulatory Integrative and Comparative Physiology 2017-03-30
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