Jun Dang

Dr. Jun Dang

Qinghai Provincial Key Laboratory of Tibetan Medicine Research, Key Laboratory of Tibetan Medicine Research, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810001, China
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2021 in Journal of Chromatography A
Verified
Journal Article
Closed access
YDYangzom Dawa
Yangzom Dawa
YDYurong Du
Yurong Du
QWQi Wang
Qi Wang
CCChengbiao Chen
Chengbiao Chen
DZDenglang Zou
Denglang Zou
Jun DangJun Dang
Jun Dang

6 August 2016 in Botanical Studies
Verified
Journal Article
Open access
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QSQiang-Qiang Shi
Qiang-Qiang Shi
Jun DangJun Dang
Jun Dang
HWHuai-Xiu Wen
Huai-Xiu Wen
XYXiang Yuan
Xiang Yuan
YTYan-duo Tao
Yan-duo Tao
QWQilan Wang
Qilan Wang
Dracocephalum heterophyllum was a traditional Tibetan medicine possesses various pharmacological effects involved in anti-inflammatory, antibacterial activities. However, its anti-hepatitis, antioxidant activity and bioactive compounds have not been reported, the objective of this research work was to investigate the pharmacological activity and bioactive compounds of D. heterophyllum extracts. In the present study, the anti-hepatics and antioxidant activities of four D. heterophyllum extracts (i.e. petroleum ether extracts, ethyl acetate extracts, n-BuOH extracts, and water extracts) were conducted. The main chemical constituent of petroleum ether and ethyl acetate extracts were also isolated using chromatographic techniques and identified by NMR spectroscopic methods. The anti-hepatitis assay showed that the petroleum ether and ethyl acetate extracts of D. heterophyllum significantly prolonged the mean survival times and reduced the mortality of mouse hepatitis model induced by concanavalin A (ConA). The levels of alanine transaminase, aspartate transaminase in blood serum could be decreased obviously by ethyl acetate extracts compared with ConA group (P < 0.01). The histological analysis demonstrated that the ethyl acetate extracts could inhibit apoptosis and necrosis caused by ConA. In addition, the antioxidant activities of the four extracts of D. heterophyllum were measured by DPPH assay, ABTS assay, anti-lipidperoxidation assay, ferric reducing antioxidant power assay, ferrous metal ions chelating assay and determination of total phenolic contents. The results showed that the ethyl acetate extract had the highest antioxidant activities, followed by petroleum ether extract. Finally, nine mainly compounds were isolated from the Petroleum ether and ethyl acetate extracts, including four triterpenes: oleanolic acid (1), ursolic acid (2), pomolic acid (3), 2α- hydroxyl ursolic acid (4), three flavonoids: apigenin-7-O-rutinoside (5), luteolin (8), diosmetin (9) and two phenolic acids: rosmarinic acid (6), methyl rosmarinate (7). The Ethyl acetate extract of D. heterophyllum had the highest anti-hepatitis and antioxidants activities, followed by petroleum ether extract. The bioactive substances may be triterpenes, flavonoids and phenolic acids, the ethyl acetate extracts of D. heterophyllum may be possible candidates in developing anti-hepatitis medicine.

1 September 2018 in Journal of Chromatography B
Verified
Journal Article
Closed access
Jun DangJun Dang
Jun Dang
LZLi Zhang
Li Zhang
YSYun Shao
Yun Shao
LMLijuan Mei
Lijuan Mei
ZLZenggen Liu
Zenggen Liu
YTYanduo Tao
Yanduo Tao

11 November 2017 in Letters in Applied Microbiology
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Journal Article
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JPJinjin Pei
Jinjin Pei
ZFZ. Feng
Z. Feng
TRT. Ren
T. Ren
HSH. Sun
H. Sun
HHH. Han
H. Han
YTY. Tao
Y. Tao
The Andrias davidianus has been known as a traditional Chinese medicine for a long time. Its blood is considered as a waste or by‐product of the meat production industry. Although there are reports on isolation of the antimicrobial peptides from different resources, there are no reports of their isolation from A. davidianus blood. In this work, an antimicrobial peptide, andricin B, was isolated from the blood of A. davidianus by an innovative method in which the magnetic liposome adsorption was combined with reversed‐phase high‐performance liquid chromatography. The structure, antimicrobial activity and safety of andricin B were further investigated. Amino acid sequence was determined by N‐terminal sequencing and found to be Gly‐Leu‐Thr‐Arg‐Leu‐Phe‐Ser‐Val‐Ile‐Lys. Circular dichroism (CD) spectra and prediction of three‐dimensional structure by bioinformatics software suggested the presence of a well‐defined random coil conformation. Andricin B was found to be active against all bacteria tested in this study as well as some fungi. The minimum inhibitory concentrations (MICs) were in the range 8–64 μg ml−1. Moreover, the haemolytic testing also suggested that andricin B could be considered safe at the MICs. Finally, andricin B was shown to inhibit the growth of Staphylococcus aureus in the cooked meat of A. davidianus. This study shows that andricin B is a promising novel antimicrobial peptide that may provide further insights towards the development of new drugs. Significance and Impact of the Study This is the pioneer study on screening and isolation of antimicrobial peptide from the blood of Andrias davidianus. Here, we have developed a novel method by combining magnetic liposomes adsorption with reversed‐phase high‐performance liquid chromatography to purify and screen the antimicrobial peptides. From this screen, we identified a novel antimicrobial peptide which we name as andricin B. Andricin B is unique as it checks the growth of both Gram‐positive and Gram‐negative bacteria as well as few fungal species.

30 August 2017 in Journal of Separation Science
Verified
Journal Article
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LJLijin Jiao
Lijin Jiao
YTYanduo Tao
Yanduo Tao
WWWeidong Wang
Weidong Wang
YSYun Shao
Yun Shao
LMLijuan Mei
Lijuan Mei
Jun DangJun Dang
Jun Dang

21 November 2018 in Journal of Separation Science
Verified
Journal Article
Closed access
PDF file
Jun DangJun Dang
Jun Dang
LZLi Zhang
Li Zhang
QWQilan Wang
Qilan Wang
LMLijuan Mei
Lijuan Mei
HYHuilan Yue
Huilan Yue
YTYanduo Tao
Yanduo Tao