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Author:

He Qingfeng (He Qingfeng.) | Luo Yunjing (Luo Yunjing.) (Scholars:罗云敬) | Shi Jianlong (Shi Jianlong.) | Tang Xiaoyu (Tang Xiaoyu.) | Wei Anqi (Wei Anqi.)

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PubMed

Abstract:

Peroxynitrite is known as a strong deleterious species that may readily trigger several geriatric diseases via injuring cellular constituents. Proanthocyanidins, a biological flavonoids constituent of Pinus sylvestris L. bark, has been attributed a large variety of pharmacological functions to its antioxidant potential. The results revealed that peroxynitrite could cause the generation of hydroxyl radical, the breakage of φX-174 plasmid DNA brand as well as the nitration of L-tyrosine. However, pine (Pinus sylvestris L.) bark proanthocyanidins extracts at low concentration range markedly inhibited the peroxynitrite -induced the formation of open circular DNA form (IC50 = 5.03±0.39 mg/mL). The 3-Nitro-L-tyrosine generated by the reaction of peroxynitrite with L-tyrosine was reduced by PBP (IC50 = 1.01±0.01 mg/mL). Besides, electron spin resonance spectroscopy data indicates that the intensive signal of dimethyl pyridine N-oxide hydroxyl radical adduct from peroxynitrite was reversed by pine bark proanthocyanidins extracts (IC50 =1.02±0.04 mg/mL). Moreover, the obtained data shows that PBP provides more efficient protection against peroxynitrite than that of ascorbic acid. Together, the present study suggests that pine bark proanthocyanidins could exert potent preventive activity against peroxynitrite -elicited cytotoxicity on the biomacromolecules, a study-worthy finding with pharmacological importance.

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Author Community:

  • [ 1 ] [He Qingfeng]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 2 ] [Luo Yunjing]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 3 ] [Shi Jianlong]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 4 ] [Tang Xiaoyu]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China
  • [ 5 ] [Wei Anqi]College of Life Science and Bioengineering, Beijing University of Technology, Beijing, China

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Source :

Pakistan journal of pharmaceutical sciences

ISSN: 1011-601X

Year: 2020

Issue: 1

Volume: 33

Page: 141-148

0 . 8 0 0

JCR@2022

ESI Discipline: PHARMACOLOGY & TOXICOLOGY;

ESI HC Threshold:105

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count:

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 3

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