Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2018 Sep 27;9:1092. doi: 10.3389/fphar.2018.01092

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

Copyright © 2018 Zheng, Lin, Lin, Lin, Thapa, Lin, Lian, Liu, Chen and Li.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

PMC Copyright notice

CCK-8 assay showed that SH treatment improved the cell viability of H9C2 post CoCl₂-induced hypoxia. (A) H9C2 were treated with various concentrations of CoCl₂ (0, 200, 400, 600, 800, 1000, 1200, and 1400 μM, n = 6 in each concentration of CoCl₂) alone for 24 h, the concentration of 1000 μM CoCl₂ resulted in half cell death. ^∗Compared with 0 μM CoCl₂ treatment, p < 0.05. (B) H9C2 were treated with various concentrations of SH (0, 10, 20, 30, 40, 50, 60, 70, and 80 μg/ml, n = 6 in each concentration of SH) alone for 24 h. ^∗Compared with 0 μg/mL SH treatment, p < 0.05. (C) The H9C2 induced hypoxia by CoCl₂ were treated with SH (0, 10, 20, 30, and 40 μg/mL, n = 6 in each concentration of SH) for 24 h, respectively. ^∗Compared with 0 μg/mL SH treatment, p < 0.05. ^#Compared with 30 μg/ml SH treatment, p > 0.05.