Branislava Daskalović
Research Subjects
Research Interests
Branislava Daskalović has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
- Davor Mrda
University Hospital Medical Center Bežanijska Kosa, 11000 Belgrade, Serbia
1 shared publication - Djordje Kralj
Department of Gastroenterology and Hepatology, University Hospital Medical Center “Zvezdara”, 11000 Belgrade, Serbia
1 shared publication - Ivana Pantic
Clinic for Gastroenterology and Hepatology, University Clinical Center of Serbia, 11000 Belgrade, Serbia
1 shared publication - Jovana Lalatović
University Hospital Medical Center Bežanijska Kosa, 11000 Belgrade, Serbia
1 shared publication - Marija Brankovic
University Hospital Medical Center Bežanijska Kosa, 11000 Belgrade, Serbia
1 shared publication - Marija Dukić
University Hospital Medical Center Bežanijska Kosa, 11000 Belgrade, Serbia
1 shared publication
Latest Publications
- Open Access
- 14 May 2024
- Published by MDPI AG in Antioxidants
- Vol. 13 (5) , 600
Therapeutic Potential of Palmitoylethanolamide in Gastrointestinal Disorders
Palmitoylethanolamide (PEA) is an endocannabinoid-like bioactive lipid mediator belonging to the family of N-acylethanolamines, most abundantly found in peanuts and egg yolk. When the gastrointestinal (GI) effects of PEA are discussed, it must be pointed out that it affects intestinal motility but also modulates gut microbiota. This is due to anti-inflammatory, antioxidant, analgesic, antimicrobial, and immunomodulatory features. Additionally, PEA has shown beneficial effects in several GI diseases, particularly irritable bowel syndrome and inflammatory bowel diseases, as various studies have shown, and it is important to emphasize its relative lack of toxicity, even at high dosages. Unfortunately, there is not enough endogenous PEA to treat disturbed gut homeostasis, even though it is produced in the GI tract in response to inflammatory stimuli, so exogenous intake is mandatory to achieve homeostasis. Intake of PEA could be through animal and/or vegetable food, but bearing in mind that a high dosage is needed to achieve a therapeutic effect, it must be compensated through dietary supplements. There are still open questions pending to be answered, so further studies investigating PEA’s effects and mechanisms of action, especially in humans, are crucial to implementing PEA in everyday clinical practice.
- 14 May 2024
- Published by MDPI AG in Antioxidants
- Vol. 13 (5) , 600
Open AccessTherapeutic Potential of Palmitoylethanolamide in Gastrointestinal Disorders
Palmitoylethanolamide (PEA) is an endocannabinoid-like bioactive lipid mediator belonging to the family of N-acylethanolamines, most abundantly found in peanuts and egg yolk. When the gastrointestinal (GI) effects of PEA are discussed, it must be pointed out that it affects intestinal motility but also modulates gut microbiota. This is due to anti-inflammatory, antioxidant, analgesic, antimicrobial, and immunomodulatory features. Additionally, PEA has shown beneficial effects in several GI diseases, particularly irritable bowel syndrome and inflammatory bowel diseases, as various studies have shown, and it is important to emphasize its relative lack of toxicity, even at high dosages. Unfortunately, there is not enough endogenous PEA to treat disturbed gut homeostasis, even though it is produced in the GI tract in response to inflammatory stimuli, so exogenous intake is mandatory to achieve homeostasis. Intake of PEA could be through animal and/or vegetable food, but bearing in mind that a high dosage is needed to achieve a therapeutic effect, it must be compensated through dietary supplements. There are still open questions pending to be answered, so further studies investigating PEA’s effects and mechanisms of action, especially in humans, are crucial to implementing PEA in everyday clinical practice.