A standardized notoginseng extract exerts cardioprotection by attenuating apoptosis under endoplasmic reticulum stress conditions. (June 2015)
- Record Type:
- Journal Article
- Title:
- A standardized notoginseng extract exerts cardioprotection by attenuating apoptosis under endoplasmic reticulum stress conditions. (June 2015)
- Main Title:
- A standardized notoginseng extract exerts cardioprotection by attenuating apoptosis under endoplasmic reticulum stress conditions
- Authors:
- Wang, Li-Chao
Zhang, Wen-Song
Liu, Qun
Li, Jia
Alolga, Raphael N.
Liu, Kang
Liu, Bao-Lin
Li, Ping
Qi, Lian-Wen - Abstract:
- Highlights: RGSE attenuated acute myocardial infarction-induced heart injury. RGSE inhibited oxidative stress and apoptosis during AMI in vivo and in vitro . TXNIP-NLRP3-IL-1β signaling, for the first time, was revealed to be activated in AMI, promoting cell death in the end. RGSE exerted cardioprotection by suppression of TXNIP/NLRP3 activation during ER stress. Ginsenosides Rh4, Rg5, Rk3, and Rk1 were the most abundant, and notoginsenoside T5/isomer was first identified in steamed notoginseng. Abstract: Panax notoginseng possesses therapeutic potential for cardiovascular disorders. Endoplasmic reticulum (ER) stress plays a critical role in cardiovascular disease. Here we show that a rare ginsenoside-standardized extract (RGSE) from notoginseng exerts cardioprotection via attenuating ER stress-associated apoptosis. A total of 18 ginsenosides with a concentration of 816.75 mg/g were characterized and quantified in RGSE. Ginsenoside Rh4, Rg5, Rk3, and Rk1 were the most abundant. RGSE at 50 and 100 mg/kg significantly attenuated myocardial infarction and improved cardiac function in acute myocardial infarction (AMI). RGSE also prevented myocardial ischemia-induced oxidative stress and apoptosis in vivo and in vitro . In addition, RGSE decreased the overexpression of GRP78, GRP94 and CHOP, and inhibited the phosphorylation of PERK and IRE1α in ER stress. Further investigation revealed that RGSE effectually inactivated TXNIP/NLRP3 signaling pathway in AMI hearts. TheseHighlights: RGSE attenuated acute myocardial infarction-induced heart injury. RGSE inhibited oxidative stress and apoptosis during AMI in vivo and in vitro . TXNIP-NLRP3-IL-1β signaling, for the first time, was revealed to be activated in AMI, promoting cell death in the end. RGSE exerted cardioprotection by suppression of TXNIP/NLRP3 activation during ER stress. Ginsenosides Rh4, Rg5, Rk3, and Rk1 were the most abundant, and notoginsenoside T5/isomer was first identified in steamed notoginseng. Abstract: Panax notoginseng possesses therapeutic potential for cardiovascular disorders. Endoplasmic reticulum (ER) stress plays a critical role in cardiovascular disease. Here we show that a rare ginsenoside-standardized extract (RGSE) from notoginseng exerts cardioprotection via attenuating ER stress-associated apoptosis. A total of 18 ginsenosides with a concentration of 816.75 mg/g were characterized and quantified in RGSE. Ginsenoside Rh4, Rg5, Rk3, and Rk1 were the most abundant. RGSE at 50 and 100 mg/kg significantly attenuated myocardial infarction and improved cardiac function in acute myocardial infarction (AMI). RGSE also prevented myocardial ischemia-induced oxidative stress and apoptosis in vivo and in vitro . In addition, RGSE decreased the overexpression of GRP78, GRP94 and CHOP, and inhibited the phosphorylation of PERK and IRE1α in ER stress. Further investigation revealed that RGSE effectually inactivated TXNIP/NLRP3 signaling pathway in AMI hearts. These observations suggest a novel role for notoginseng in regulating AMI. … (more)
- Is Part Of:
- Journal of functional foods. Volume 16(2015)
- Journal:
- Journal of functional foods
- Issue:
- Volume 16(2015)
- Issue Display:
- Volume 16, Issue 2015 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 2015
- Issue Sort Value:
- 2015-0016-2015-0000
- Page Start:
- 20
- Page End:
- 27
- Publication Date:
- 2015-06
- Subjects:
- Acute myocardial infarction -- Apoptosis -- Cardioprotection -- Endoplasmic reticulum stress -- Rare ginsenoside-standardized extract -- Steamed Panax notoginseng
Notoginsenoside R1 (PubChem CID: 441934) -- Ginsenoside Rb1 (PubChem CID: 9898279) -- Ginsenoside Rg1 (PubChem CID: 441923) -- 20(S)-Ginsenoside Rg3 (PubChem CID: 9918693) -- 20(R)-Ginsenoside Rg3 (PubChem CID: 46887680) -- Ginsenoside Rg5 (PubChem CID: 6450175) -- Ginsenoside Rh4, (PubChem CID: 21599928) -- BAPTA-AM (PubChem CID: 2293) -- Diltiazem hydrochloride (PubChem CID: 62920) -- Tauroursodeoxycholic acid (PubChem CID: 9848818)
AMI acute myocardial infarction -- +dP/dtmax maximal rate of pressure development for contraction -- −dP/dtmax maximal rate of pressure development for relaxation -- ER endoplasmic reticulum -- LAD left anterior descending -- LVEDP left ventricular end-diastolic pressure -- LVSP left ventricular systolic pressure -- NG notoginsenoside -- OGD oxygen and glucose deprivation -- RGSE rare ginsenoside-standardized extract -- TUDCA tauroursodeoxycholic acid
Functional foods -- Analysis -- Periodicals
Food -- Biotechnology -- Periodicals
Nutrition -- Periodicals
613.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/17564646 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jff.2015.04.018 ↗
- Languages:
- English
- ISSNs:
- 1756-4646
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 4986.807000
British Library DSC - BLDSS-3PM
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