» Articles » PMID: 35310030

Nature Against Diabetic Retinopathy: A Review on Antiangiogenic, Antioxidant, and Anti-Inflammatory Phytochemicals

Abstract

. Diabetes mellitus (DM), hyperglycemia, and hypertension can result in diabetic retinopathy (DR), which is a major cause of blindness on a global scale. Development of DR is associated with decreased endothelial cells, increased basal membrane thickness, permeation of the retinal blood barrier, and neovascularization in patients. The purpose of the present review is to provide an overview of the findings regarding applications of phytochemicals for DR treatment and could be a beneficial resource for further clinical studies and also a basis for pharmaceutical purposes for drug design. . A narrative literature review was performed from electronic databases including Web of Science, PubMed, and Scopus to analyze the effects of different phytochemicals to prevent or treat oxidation, angiogenesis, and inflammation in diabetic retinopathy. The inclusion criteria were original studies, which included the effects of different phytochemicals on diabetic retinopathy. The exclusion criteria included studies other than original articles, studies which assessed the effects of phytochemicals on nondiabetic retinopathy, and studies which used phytochemical-rich extracts. . Studies have shown that increased levels of inflammatory cytokines, angiogenic, and oxidative stress factors are involved in the progression and pathogenesis of DR. Therefore, phytochemicals with their anti-inflammatory, antiangiogenic, and antioxidant properties can prevent DR progression and retinal damage through various cellular mechanisms. It is also shown that some phytochemicals can simultaneously affect the inflammation, oxidation, and angiogenesis in DR.

Citing Articles

Unlocking the Potential: How Flavonoids Affect Angiogenesis, Oxidative Stress, Inflammation, Proliferation, Invasion, and Alter Receptor Interactions in Endometriosis.

Goleij P, Khandan M, Tabari M, Sanaye P, Alijanzadeh D, Soltani A Food Sci Nutr. 2025; 13(1):e4607.

PMID: 39803270 PMC: 11716992. DOI: 10.1002/fsn3.4607.


Exploring the Molecular Underpinnings of Skin Regeneration and Wound Healing: The Role of Renin Angiotensin.

Qoreishi S, Tabari M, Gaman M, Kazeminejad A Avicenna J Med Biotechnol. 2024; 16(3):146-155.

PMID: 39132629 PMC: 11316511. DOI: 10.18502/ajmb.v16i3.15740.


β-Asarone Alleviates High-Glucose-Induced Oxidative Damage via Inhibition of ROS Generation and Inactivation of the NF-κB/NLRP3 Inflammasome Pathway in Human Retinal Pigment Epithelial Cells.

Park C, Cha H, Hwangbo H, Bang E, Hong S, Song K Antioxidants (Basel). 2023; 12(7).

PMID: 37507949 PMC: 10376195. DOI: 10.3390/antiox12071410.


The signaling pathways of traditional Chinese medicine in treating diabetic retinopathy.

Li W, Xing Q, Liu Z, Liu R, Hu Y, Yan Q Front Pharmacol. 2023; 14:1165649.

PMID: 37405050 PMC: 10315578. DOI: 10.3389/fphar.2023.1165649.

References
1.
Kang M, Park S, Kim Y, Lee E, Antika L, Kim D . Dietary Compound Chrysin Inhibits Retinal Neovascularization with Abnormal Capillaries in db/db Mice. Nutrients. 2016; 8(12). PMC: 5188437. DOI: 10.3390/nu8120782. View

2.
Echeverria F, Valenzuela R, Hernandez-Rodas M, Valenzuela A . Docosahexaenoic acid (DHA), a fundamental fatty acid for the brain: New dietary sources. Prostaglandins Leukot Essent Fatty Acids. 2017; 124:1-10. DOI: 10.1016/j.plefa.2017.08.001. View

3.
Zhang H, Shi K, Baskota A, Zhou F, Chen Y, Tian H . Silybin reduces obliterated retinal capillaries in experimental diabetic retinopathy in rats. Eur J Pharmacol. 2014; 740:233-9. DOI: 10.1016/j.ejphar.2014.07.033. View

4.
Roohbakhsh A, Parhiz H, Soltani F, Rezaee R, Iranshahi M . Molecular mechanisms behind the biological effects of hesperidin and hesperetin for the prevention of cancer and cardiovascular diseases. Life Sci. 2015; 124:64-74. DOI: 10.1016/j.lfs.2014.12.030. View

5.
Yu C, Zhang P, Lou L, Wang Y . Perspectives Regarding the Role of Biochanin A in Humans. Front Pharmacol. 2019; 10:793. PMC: 6639423. DOI: 10.3389/fphar.2019.00793. View