Berberine Ameliorates Brain Inflammation in Poloxamer 407-Induced Hyperlipidemic Rats
- Affiliations
-
- 1Department of Cardiovascular Neurologic Disease (Stroke Center), College of Korean Medicine, Kyung Hee University, Seoul, Korea.
- 2Department of Physiology, College of Medicine, Kyung Hee University, Seoul, Korea. s07@naver.com
- 3College of Culture and Sports, Division of Global Sport Studies, Korea University, Sejong, Korea.
- 4Department of Psychiatry, Myongji Hospital, College of Medicine, Hanyang University, Goyang, Korea.
- 5Department of Kinesiology, College of Public Health and Cardiovascular Research Center, Lewis Kate School of Medicine, Temple University, Philadelphia, PA, USA.
Abstract
- PURPOSE
Hyperlipidemia, which promotes the development of atherosclerosis, ischemic stroke, and other forms of brain injury, can be induced by poloxamer-407. Berberine is a primary pharmacological active component of Coptidis Rhizoma that has a number of therapeutic activities. This study investigated the effects of berberine on poloxamer-407-induced brain inflammation by evaluating its effects on short-term memory, cell proliferation, inflammation, and apoptosis in the hippocampus.
METHODS
To induce hyperlipidemia in a rat model, 500 mg/kg of poloxamer-407 was injected intraperitoneally. Berberine was orally administered to the rats in the berberine-treated groups once a day for 4 weeks. The step-down task avoidance task was performed to measure short-term memory. An analysis of serum lipids, immunohistochemistry for 5-bromo-2"²-deoxyuridine, glial fibrillary acidic protein (GFAP), and ionized calcium-binding adapter molecule 1 (Iba1) in the dentate gyrus, and western blot analysis for Bax, Bcl-2, and cytochrome c in the hippocampus were performed.
RESULTS
In hyperlipidemic rats, berberine reduced the levels of triglycerides, total cholesterol, and low-density lipoprotein cholesterol and increased the level of high-density lipoprotein cholesterol in hyperlipidemic rats. Berberine also increased cell proliferation and short-term memory, as well as decreasing the expression of GFAP, Iba1, Bax, and cytochrome c and increasing Bcl-2 expression.
CONCLUSIONS
Berberine treatment improved short-term memory in hyperlipidemia by increasing neuronal proliferation and inhibiting neuronal apoptosis. Berberine treatment also improved lipid metabolism.