Planta Med 2016; 82(01/02): 46-57
DOI: 10.1055/s-0035-1557829
Biological and Pharmacological Activitiy
Original Papers
Georg Thieme Verlag KG Stuttgart · New York

Pheophorbide a from Capsosiphon fulvescens Inhibits Advanced Glycation End Products Mediated Endothelial Dysfunction

Authors

  • Chung-Oui Hong*

    1   Department of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul, South Korea
  • Mi-Hyun Nam*

    1   Department of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul, South Korea
  • Ji-Sun Oh

    1   Department of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul, South Korea
  • Jin-Won Lee

    2   Department of Food and Biotechnology, College of Science and Engineering, Hankyung National University, Anseong-si, Kyonggi-do, South Korea
  • Cheong-Tae Kim

    3   Nong shim Co. 370, Shindaebang-dong, Dongjak-ku, Seoul, South Korea
  • Kwon-Woo Park

    4   Division of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul, South Korea
  • Dong-Ho Lee

    4   Division of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul, South Korea
  • Kwang-Won Lee

    1   Department of Biotechnology, College of Life Science and Biotechnology, Korea University, Seoul, South Korea
Further Information

Publication History

received 30 November 2014
revised 22 June 2015

accepted 09 July 2015

Publication Date:
26 August 2015 (online)

Abstract

During hyperglycemia, the first step toward the formation of advanced glycation end products is the nonenzymatic glycation between the carbonyl group of a sugar and the primary amino group of a protein. Advanced glycation end products are then produced through more complex reactions. Reactive oxygen species derived from advanced glycation end products may play a key role in inflammation of the endothelium, leading to the complications seen in diabetes. Glycolaldehyde-induced advanced glycation end products have been reported to express proinflammatory cytokines, such as tumor necrosis factor-α and interleukin-1β. This study focused on Capsosiphon fulvescens, a Capsosiphonaceae type of green algae that has shown potential as a functional food material. Pheophorbide a, an anti-glycation compound, was isolated from C. fulvescens by extraction using a mixture of ethanol and water, followed by column fractionation of the resulting extract. The compound separated from C. fulvescens was identified by means of high-performance liquid chromatography combined with mass spectrometry. Pheophorbide a showed scavenging activity of the intracellular reactive oxygen species as well as monocyte adhesiveness inhibitory activity on the human myelomonocytic cell line (THP-1) and human umbilical vein endothelial cells cocultivation system. The mRNA levels of inflammation-related genes such as monocyte chemoattractant protein-1 and interleukin-6 were significantly decreased by pheophorbide a, and advanced glycation end products-stimulated tumor necrosis factor-α and interleukin-1β were downregulated as well. These results indicate that pheophorbide a has significant reactive oxygen species-scavenging activity, monocyte adhesive inhibitory activity, and downregulatory activity of cytokines related to inflammation affecting the endothelium. Pheophorbide a could therefore be a promising candidate for modulating endothelial cell dysfunction.

* These two authors have contributed equally to this work and should be considered co-first authors.