4.7 Article

Dual effect of the herbal matcha green tea (Camellia sinensis L. kuntze) supplement in EA.hy926 endothelial cells and Artemia salina

Journal

JOURNAL OF ETHNOPHARMACOLOGY
Volume 298, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jep.2022.115564

Keywords

Mitochondrial dysfunction; Camellia sinensis; Oxidative stress; Hyperglycemia

Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  2. Fundacao de Amparo a Pesquisa do Estado do Rio Grande do Sul (FAPERGS)
  3. Coordenacao de Apoio de Pessoal de Nivel Superior (CAPES)
  4. CAPES Research Fellowship
  5. CNPq Research Fellowship [3033383/2015-1]

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This study aimed to evaluate the efficacy and safety of matcha green tea supplements in endothelial cells under hyperglycemic conditions. The results showed that the supplement had antioxidant activity but also induced toxicity in the endothelial cells.
Ethnopharmacological relevance: Matcha green tea (Camellia sinensis) based-supplements have been widely used since they present a greater content of phenolic compounds than traditional green tea, which is popularly used in the treatment of diabetes. However, there are few studies on the effectiveness and safety of matcha supplements. Aim of the study: This work aimed to evaluate the efficacy and safety of this supplement in endothelial cells (EA. hy926) in the hyperglycemic model and in vivo Artemia salina. Materials and methods: To assess the effect of Matcha herbal supplement (MHS), EA. hy926 endothelial cells were treated with 20 mu g/mL of MHS for 24 h, in a hyperglycemic medium with 35 mM glucose. After treatment, cells were trypsinized and centrifuged at 4 ? and 47xg for 5 min. The pellet was used to determine the reaction products to thiobarbituric acid and the levels of nitric oxide. Electron transport chain activity and ATP levels were also evaluated. Intracellular pH, apoptosis, and mitochondrial membrane depolarization were evaluated by flow cytometry. MHS chemical characterization was performed by HPLC-UV and total phenolic content analysis. The evaluation of the antioxidant capacity of MHS was performed by 2,2-diphenyl-1-picrylhydrazyl radical scavenger assay. To determine the in vivo acute toxicity of MHS, an A. salina assay was conducted, using 0,2 mL of different concentrations of MHS (10, 50, 100, 250, 500, 750 and 1000 mu g/mL). The LD50 values were obtained by interpolation of 50% (y = 50) of the dead individuals in the trend curves. Results: Our data showed that MHS was able to avoid oxidative and nitrosative stress induced by hyperglycemia, demonstrating important antioxidant activity. However, it was observed that MHS reduced up to 90% the activity of the four-electron transport complexes, reducing the ATP production of the endothelial cells. In the toxicity assay performed in Artemia salina, MHS showed mild toxicity (LD50 = 0,4 mg/mL). The major com-pounds found in MHS were epigallocatechin gallate, epicatechin, rutin, kaempferol, and quercetin. Conclusions: This data draws attention to the fact that supplements with high content of phenolic compounds, capable of avoiding oxidative and nitrosative stress can have a dual effect and, simultaneously to antioxidant activity, can induce toxicity in different cell types.

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