TY - JOUR
T1 - Protection of dilator function of coronary arteries from homocysteine by tetramethylpyrazine
T2 - Role of ER stress in modulation of BK Ca channels
AU - Sun, Wen Tao
AU - Wang, Xiang Chong
AU - Novakovic, Aleksandra
AU - Wang, Jun
AU - He, Guo Wei
AU - Yang, Qin
N1 - Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/2
Y1 - 2019/2
N2 - Objectives: We recently reported the involvement of ER stress-mediated BK Ca channel inhibition in homocysteine-induced coronary dilator dysfunction. In another study, we demonstrated that tetramethylpyrazine (TMP), an active ingredient of the Chinese herb Chuanxiong, possesses potent anti-ER stress capacity. The present study investigated whether TMP protects BK Ca channels from homocysteine-induced inhibition and whether suppression of ER stress is a mechanism contributing to the protection. Furthermore, we explored the signaling transduction involved in TMP-conferred protection on BK Ca channels. Methods: BK Ca channel-mediated relaxation was studied in porcine small coronary arteries. Expressions of BK Ca channel subunits, ER stress molecules, and E3 ubiquitin ligases, as well as BK Ca ubiquitination were determined in porcine coronary arterial smooth muscle cells (PCASMCs). Whole-cell BK Ca currents were recorded. Results: Exposure of PCASMCs to homocysteine or the chemical ER stressor tunicamycin increased the expression of ER stress molecules, which was significantly inhibited by TMP. Suppression of ER stress by TMP preserved the BK Ca β1 protein level and restored the BK Ca current in PCASMCs, concomitant with an improved BK Ca -mediated dilatation in coronary arteries. TMP attenuated homocysteine-induced BK Ca β1 protein ubiquitination, in which inhibition of ER stress-mediated FoxO3a activation and FoxO3a-dependent atrogin-1 and Murf-1 was involved. Conclusions: Reversal of BK Ca channel inhibition via suppressing ER stress-mediated loss of β1 subunits contributes to the protective effect of TMP against homocysteine on coronary dilator function. Inhibition of FoxO3a-dependent ubiquitin ligases is involved in TMP-conferred normalization of BK Ca β1 protein level. These results provide new mechanistic insights into the cardiovascular benefits of TMP.
AB - Objectives: We recently reported the involvement of ER stress-mediated BK Ca channel inhibition in homocysteine-induced coronary dilator dysfunction. In another study, we demonstrated that tetramethylpyrazine (TMP), an active ingredient of the Chinese herb Chuanxiong, possesses potent anti-ER stress capacity. The present study investigated whether TMP protects BK Ca channels from homocysteine-induced inhibition and whether suppression of ER stress is a mechanism contributing to the protection. Furthermore, we explored the signaling transduction involved in TMP-conferred protection on BK Ca channels. Methods: BK Ca channel-mediated relaxation was studied in porcine small coronary arteries. Expressions of BK Ca channel subunits, ER stress molecules, and E3 ubiquitin ligases, as well as BK Ca ubiquitination were determined in porcine coronary arterial smooth muscle cells (PCASMCs). Whole-cell BK Ca currents were recorded. Results: Exposure of PCASMCs to homocysteine or the chemical ER stressor tunicamycin increased the expression of ER stress molecules, which was significantly inhibited by TMP. Suppression of ER stress by TMP preserved the BK Ca β1 protein level and restored the BK Ca current in PCASMCs, concomitant with an improved BK Ca -mediated dilatation in coronary arteries. TMP attenuated homocysteine-induced BK Ca β1 protein ubiquitination, in which inhibition of ER stress-mediated FoxO3a activation and FoxO3a-dependent atrogin-1 and Murf-1 was involved. Conclusions: Reversal of BK Ca channel inhibition via suppressing ER stress-mediated loss of β1 subunits contributes to the protective effect of TMP against homocysteine on coronary dilator function. Inhibition of FoxO3a-dependent ubiquitin ligases is involved in TMP-conferred normalization of BK Ca β1 protein level. These results provide new mechanistic insights into the cardiovascular benefits of TMP.
KW - Ca -activated K channels
KW - Coronary circulation
KW - Endoplasmic reticulum stress
KW - Homocysteine
KW - Tetramethylpyrazine
UR - https://www.scopus.com/pages/publications/85055888753
U2 - 10.1016/j.vph.2018.10.009
DO - 10.1016/j.vph.2018.10.009
M3 - 文章
C2 - 30389615
AN - SCOPUS:85055888753
SN - 1537-1891
VL - 113
SP - 27
EP - 37
JO - Vascular Pharmacology
JF - Vascular Pharmacology
ER -