黑料网

ISSN: 2167-065X

Clinical Pharmacology & Biopharmaceutics
黑料网

Our Group organises 3000+ Global Events every year across USA, Europe & Asia with support from 1000 more scientific Societies and Publishes 700+ 黑料网 Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.

黑料网 Journals gaining more Readers and Citations
700 Journals and 15,000,000 Readers Each Journal is getting 25,000+ Readers

This Readership is 10 times more when compared to other Subscription Journals (Source: Google Analytics)
Citations : 790

Indexed In
  • CAS Source Index (CASSI)
  • Index Copernicus
  • Google Scholar
  • Sherpa Romeo
  • Genamics JournalSeek
  • RefSeek
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • Publons
  • Euro Pub
  • ICMJE
Share This Page

Artemisinin protected neuronal cells from oxidative insult via the MAPK pathway

7th Annual Global Pharma Summit

Wenhua Zheng, Fang Jiankang, Wan Pei, Xu Jinying, Cheong-Meng Chong and Philip Lazarovici

University of Macau, China

ScientificTracks Abstracts: Clin Pharmacol Biopharm

DOI:

Abstract
Artemisinin, also known as Qinghao su, isolated from Artemisia annua, is a drug that possesses the most rapid action of all current drugs against Plasmodium falciparum malaria. It is clinically safe, potent and effective in human. At present study, we found that artemisinin promoted the survival of various cell types such as PC12 cells and primary cortical cultured neurons from oxidative insults. For example, pretreatment of PC12 cells with artemisinin significantly suppressed SNP/H2O2-induced cell death by decreasing the production of intracellular reactive oxygen species (ROS), preventing the decline of mitochondrial membrane potential, restoring abnormal changes in nuclear morphology and reducing LDH and caspase 3/7 activities. Western blotting analysis showed that artemisinin was able to stimulate the phosphorylation/activation of extracellular regulated protein kinases (ERK) kinase and CREB while had no effect on the Akt pathway. In addition, ERK signaling pathway inhibitor PD98059 blocked the protective effect of artemisinin whereas the PI3K inhibitor LY294002 had no effect. Taken together, these results suggest that artemisinin as a potential neuroprotectant is able to suppress various oxidative stress-induced neuronal cell deaths via the activation of ERK signaling. Our results offer support for the potential development of artemisinin to prevent neuronal degenerative disorders.
Biography

Wenhua Zheng is currently an Associate Professor, Principle Investigator in Faculty of Health Science, University of Macau, leading a group of scientists working on aging and neuronal degenerative disorders. He is also an Editor of “Chinese Journal of Biology” and an Adjunct Professor at RMIT University in Australia. He has obtained his Medical degree and MSc at Zhongshan University in China and PhD at McGill University, Canada. He was awarded several Post-doctoral research training positions in prestigious research institutes and universities such as NIH and McGill University. In 2015, he has joined University of Macau.

Email: wenhuaZheng@umac.mo

International Conferences 2024-25
 
Meet Inspiring Speakers and Experts at our 3000+ Global

Conferences by Country

Medical & Clinical Conferences

Conferences By Subject

Top