Antiglycation activity of Vaccinium spp. (Ericaceae) from the Sam Vander Kloet collection for the treatment of type II diabetes1This article is part of a Special Issue entitled “A tribute to Sam Vander Kloet FLS: Pure and applied research from blueberries to heathland ecology”.

Botany ◽  
2012 ◽  
Vol 90 (5) ◽  
pp. 401-406 ◽  
Author(s):  
Jonathan Ferrier ◽  
Sabrina Djeffal ◽  
Holly Porter Morgan ◽  
Sam P. Vander Kloet ◽  
Sulejman Redžić ◽  
...  

In this report, the inhibition of advanced glycation endproducts (AGEs) by extracts of leaves from a collection of six, mainly tropical, Vaccinium L. spp. (Ericaceae) was examined. Indigenous Peoples have used Vaccinium species to treat symptoms of type I and II diabetes. Sustained hyperglycaemia, often associated with diabetes, facilitates crosslinking of sugars with proteins, producing AGEs. AGEs are a therapeutic target since they are responsible for many diabetes symptoms and contribute to ageing and the development of atherosclerosis, kidney, vascular, and neurological diseases. Vaccinium barandanum S. Vidal, Vaccinium consanguineum Klotzsch, Vaccinium gaultheriifolium (Griff.) Hook. f. ex C.B. Clarke, Vaccinium poasanum Donn. Sm., Vaccinium tonkinense Dop, and Disterigma rimbachii (A.C. Sm.) Luteyn (outgroup) were collected from Sam Vander Kloet’s common garden collection. Ethanolic extracts of leaves of these Vaccinium spp. were potent inhibitors of AGEs. Vaccinium and outgroup species extracts tested in an AGE inhibition assay demonstrated concentration dependent inhibition, with a half maximal inhibitory concentration (IC50) ranging from 4.2 to 16.2 µg·mL–1. Phenolic content ranged from 258 to 626 (µg quercetin equivalents·mg extract–1). Activity and phenolic content show that these tropical accessions have a higher phenolic content (p < 0.001, t test) and AGE inhibition (p < 0.03, t test) than six temperate species from our collections in eastern North America. Significant relationships were found between IC50 and latitude of geographic origin.

Cells ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 564
Author(s):  
Haruki Watanabe ◽  
Myoungsun Son

The disruption of the immune tolerance induces autoimmunity such as systemic lupus erythematosus and vasculitis. A chromatin-binding non-histone protein, high mobility group box 1 (HMGB1), is released from the nucleus to the extracellular milieu in particular environments such as autoimmunity, sepsis and hypoxia. Extracellular HMGB1 engages pattern recognition receptors, including Toll-like receptors (TLRs) and the receptor for advanced glycation endproducts (RAGE). While the HMGB1-RAGE axis drives inflammation in various diseases, recent studies also focus on the anti-inflammatory effects of HMGB1 and RAGE. This review discusses current perspectives on HMGB1 and RAGE’s roles in controlling inflammation and immune tolerance. We also suggest how RAGE heterodimers responding microenvironments functions in immune responses.


Heliyon ◽  
2020 ◽  
Vol 6 (11) ◽  
pp. e05364
Author(s):  
Isabella M. Atzeni ◽  
Jeltje Boersema ◽  
Hendri H. Pas ◽  
Gilles F.H. Diercks ◽  
Jean L.J.M. Scheijen ◽  
...  

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