Oral sophocarpine protects rat heart against pressure overload-induced cardiac fibrosis. (August 2014)
- Record Type:
- Journal Article
- Title:
- Oral sophocarpine protects rat heart against pressure overload-induced cardiac fibrosis. (August 2014)
- Main Title:
- Oral sophocarpine protects rat heart against pressure overload-induced cardiac fibrosis
- Authors:
- Li, Jun
Li, Liudong
Chu, Hongxia
Sun, Xiaojian
Ge, Zhiming - Abstract:
- <abstract> <title>Abstract</title> <p> <italic>Context</italic>: Sophocarpine, a tetracyclic quinolizidine alkaloid, is one of the most abundant active ingredients in <italic>Sophora alopecuroides</italic> Linn. (Kudouzi). Sophocarpine injection was found to have significant antiviral effects against coxsackievirus B3 and therapeutic effects for viral myocarditis in the clinic.</p> <p> <italic>Objective</italic>: This study assessed the effects of sophocapine on overload-induced cardiac fibrosis and investigated potential mechanisms.</p> <p> <italic>Materials and methods</italic>: Adult male Sprague–Dawley rats were subjected to a suprarenal abdominal aorta constriction (AC) or sham to induce sustained pressure overload. Six weeks later, rats were randomly assigned to receive sophocapine (10, 20, and 40 mg/kg, gavage) or vehicle treatment for an additional 6 weeks. Six weeks after treatment, cardiac dysfunction, cardiac coefficient, cardiac fibrosis, hydroxyproline concentration, and inflammation mediators were examined.</p> <p> <italic>Results</italic>: When compared with the model group, the left ventricular weight/body weight decreased by 25.4% and 39.0% in 20 and 40 mg/kg sophocarpine groups, respectively. The beneficial effects were associated with amelioration of left ventricular systolic pressure (LVSP) and left ventricular enddiastolic pressure (LVEDP). Moreover, pressure overload-induced cardiac fibrosis was attenuated in sophocarpine treated groups. Importantly,<abstract> <title>Abstract</title> <p> <italic>Context</italic>: Sophocarpine, a tetracyclic quinolizidine alkaloid, is one of the most abundant active ingredients in <italic>Sophora alopecuroides</italic> Linn. (Kudouzi). Sophocarpine injection was found to have significant antiviral effects against coxsackievirus B3 and therapeutic effects for viral myocarditis in the clinic.</p> <p> <italic>Objective</italic>: This study assessed the effects of sophocapine on overload-induced cardiac fibrosis and investigated potential mechanisms.</p> <p> <italic>Materials and methods</italic>: Adult male Sprague–Dawley rats were subjected to a suprarenal abdominal aorta constriction (AC) or sham to induce sustained pressure overload. Six weeks later, rats were randomly assigned to receive sophocapine (10, 20, and 40 mg/kg, gavage) or vehicle treatment for an additional 6 weeks. Six weeks after treatment, cardiac dysfunction, cardiac coefficient, cardiac fibrosis, hydroxyproline concentration, and inflammation mediators were examined.</p> <p> <italic>Results</italic>: When compared with the model group, the left ventricular weight/body weight decreased by 25.4% and 39.0% in 20 and 40 mg/kg sophocarpine groups, respectively. The beneficial effects were associated with amelioration of left ventricular systolic pressure (LVSP) and left ventricular enddiastolic pressure (LVEDP). Moreover, pressure overload-induced cardiac fibrosis was attenuated in sophocarpine treated groups. Importantly, sophocarpine (20 and 40 mg/kg) decreased pro-inflammatory cytokine levels (IL-6, 14.6% and 18.5%; IL-1β, 23.1% and 32.6%), collagen content (27.7% and 50.1%), as well as matrix metalloproteinases-2, 9 (MMP-2, 9) expression (MMP-2, 11.8% and 18.5%; MMP-9, 16.2% and 21.1%). Sophocarpine (40 mg/kg) inhibited IκB-α phosphorylation (19.0%).</p> <p> <italic>Conclusion</italic>: These findings indicated that sophocarpine potentially had antifibrotic effects. The mechanism might be due to modulation of the balance between pro-inflammatory cytokine expression and collagen content level as well as MMPs expression via the NF-κB signaling pathway.</p> </abstract> … (more)
- Is Part Of:
- Pharmaceutical biology. Volume 52:Number 8(2014:Aug.)
- Journal:
- Pharmaceutical biology
- Issue:
- Volume 52:Number 8(2014:Aug.)
- Issue Display:
- Volume 52, Issue 8 (2014)
- Year:
- 2014
- Volume:
- 52
- Issue:
- 8
- Issue Sort Value:
- 2014-0052-0008-0000
- Page Start:
- 1045
- Page End:
- 1051
- Publication Date:
- 2014-08
- Subjects:
- Pharmacognosy -- Periodicals
Materia medica, Vegetable -- Periodicals
615.321 - Journal URLs:
- http://www.tandfonline.com/toc/iphb20/current ↗
http://informahealthcare.com/journal/phb ↗
http://informahealthcare.com ↗ - DOI:
- 10.3109/13880209.2013.877038 ↗
- Languages:
- English
- ISSNs:
- 1388-0209
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6442.767000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3556.xml