Anita Aminoshariae
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Anita Aminoshariae has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
Andre Mickel
Department of Endodontics, School of Dental Medicine, Case Western Reserve University, Cleveland, Ohio
3 shared publicationsAshraf F. Fouad
Department of Endodontics, University of North Carolina, School of Dentistry, Chapel Hill, North Carolina
3 shared publicationsJames C. Kulild
Department of Endodontics, University of Missouri-Kansas City, School of Dentistry, Kansas City, Missouri
3 shared publicationsGe Jin
1 shared publicationM. Reza Aminoshariae
Department of Medicine, International American University College of Medicine, Banse, St Lucia
1 shared publicationNavid Khalighinejad
Department of Endodontics, School of Dental Medicine, Case Western Reserve University, Cleveland, Ohio
1 shared publication
Latest Publications
- 1 September 2018
- Published by Elsevier in Journal of Endodontics
- Vol. 44 (9) , 1361-1366.e3
The Impact of Endodontic Infections on the Pathogenesis of Cardiovascular Disease(s): A Systematic Review with Meta-analysis Using GRADE
- 1 September 2018
- Published by Elsevier in Journal of Endodontics
- Vol. 44 (9) , 1361-1366.e3
The Impact of Endodontic Infections on the Pathogenesis of Cardiovascular Disease(s): A Systematic Review with Meta-analysis Using GRADE
- 1 April 2017
- Published by Elsevier in Journal of Endodontics
- Vol. 43 (4) , 514-519
Association between Systemic Diseases and Endodontic Outcome: A Systematic Review
- 1 April 2017
- Published by Elsevier in Journal of Endodontics
- Vol. 43 (4) , 514-519
Association between Systemic Diseases and Endodontic Outcome: A Systematic Review
- 1 October 2016
- Published by Elsevier in Journal of Endodontics
- Vol. 42 (10) , 1427-1434
Association between Systemic Diseases and Apical Periodontitis
- 1 October 2016
- Published by Elsevier in Journal of Endodontics
- Vol. 42 (10) , 1427-1434
Association between Systemic Diseases and Apical Periodontitis
- 24 April 2013
- Vol. 44 (6) , 393
The effect of docosahexaenoic acid (DHA) on expression of IL-1ß, IL-6, IL-8, and TNF-α in normal and lipopolysaccharide (LPS)-stimulated macrophages
Differentiated macrophages (MØ) are the resident tissue phagocytes and sentinel cells of the innate immune response. These cells are major constituents of periapical granulomas. Current studies indicate these activated cells as the source of bone-resorbing cytokines in the periapical granuloma. Periapical inflammation can be mediated by proinflammatory cytokines like interleukin 1ß (IL-1ß), tumor necrosis factor α (TNF-α), IL-6, and IL-8. Reducing the production of these cytokines may be beneficial for the treatment of periapical lesions. Oils rich in omega-3 fatty acids like docosahexaenoic acid (DHA) have been linked with anti-resorptive and bone-protective effects. The purpose of this investigation was to study the effect of DHA on the expression of these cytokines by normal and lipopolysaccharide (LPS)-treated MØ. We hypothesized that pretreatment of MØ with DHA decreases the expression of pro-inflammatory cytokines induced by LPS-treated MØ. THP-1 monocytes were cultured and differentiated into MØ. DHA was added to MØ in a dose-dependent manner. MØ samples were added to the following groups: Group 1, ethanol alone as a solvent control; Group 2, 10 µg/ml of DHA (D1); Group 3, 20 µg/ml of DHA (D2); Group 4, 10 µg/ml of DHA + LPS (DL1); Group 5, 20 µg/ml of DHA + LPS (DL2); Group 6, LPS alone. Reverse transcriptase-PCR (RT-PCR) followed by ImageJ analysis was used to measure cytokine expression. The results show that IL-1ß and TNF-α levels for DL and DHA (basal) were significantly lower than the levels in LPS alone. IL-6 was increased in the DL groups. There was no significant change for IL-8. DHA at higher concentrations may selectively decrease proinflammatory cytokine production of IL-1ß and TNF-α. More studies are needed to verify the anti-inflammatory therapeutic action of agents like DHA omega-3 fatty acids.
- 24 April 2013
- Vol. 44 (6) , 393
The effect of docosahexaenoic acid (DHA) on expression of IL-1ß, IL-6, IL-8, and TNF-α in normal and lipopolysaccharide (LPS)-stimulated macrophages
Differentiated macrophages (MØ) are the resident tissue phagocytes and sentinel cells of the innate immune response. These cells are major constituents of periapical granulomas. Current studies indicate these activated cells as the source of bone-resorbing cytokines in the periapical granuloma. Periapical inflammation can be mediated by proinflammatory cytokines like interleukin 1ß (IL-1ß), tumor necrosis factor α (TNF-α), IL-6, and IL-8. Reducing the production of these cytokines may be beneficial for the treatment of periapical lesions. Oils rich in omega-3 fatty acids like docosahexaenoic acid (DHA) have been linked with anti-resorptive and bone-protective effects. The purpose of this investigation was to study the effect of DHA on the expression of these cytokines by normal and lipopolysaccharide (LPS)-treated MØ. We hypothesized that pretreatment of MØ with DHA decreases the expression of pro-inflammatory cytokines induced by LPS-treated MØ. THP-1 monocytes were cultured and differentiated into MØ. DHA was added to MØ in a dose-dependent manner. MØ samples were added to the following groups: Group 1, ethanol alone as a solvent control; Group 2, 10 µg/ml of DHA (D1); Group 3, 20 µg/ml of DHA (D2); Group 4, 10 µg/ml of DHA + LPS (DL1); Group 5, 20 µg/ml of DHA + LPS (DL2); Group 6, LPS alone. Reverse transcriptase-PCR (RT-PCR) followed by ImageJ analysis was used to measure cytokine expression. The results show that IL-1ß and TNF-α levels for DL and DHA (basal) were significantly lower than the levels in LPS alone. IL-6 was increased in the DL groups. There was no significant change for IL-8. DHA at higher concentrations may selectively decrease proinflammatory cytokine production of IL-1ß and TNF-α. More studies are needed to verify the anti-inflammatory therapeutic action of agents like DHA omega-3 fatty acids.