Black ginseng extract ameliorates hypercholesterolemia in rats

详细信息    查看全文

• 作者：Evelyn Saba¹ ; Bo Ra Jeon¹ ; Da-Hye Jeong¹ ; Kija Lee² ; Youn-Kyoung Goo³ ; Seung-Hyung Kim⁴ ; Chang-Keun Sung⁵ ; Seong-Soo Roh⁶ ; Sung Dae Kim⁷ ; Hyun-Kyoung Kim⁵ ; ^{kimhk4@empas.com" class="auth_mail" title="E-mail the corresponding author} ; Man-Hee Rhee¹ ; ^{rheemh@knu.ac.kr" class="auth_mail" title="E-mail the corresponding author}
• 关键词：black ginseng ; hypercholesterolemia ; lipogenesis ; messenger RNA
• 刊名：Journal of Ginseng Research
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：40
• 期：2
• 页码：160-168
• 全文大小：1917 K

文摘

Ginseng (Panax ginseng Meyer) is a well-characterized medicinal herb listed in the classic oriental herbal dictionary as “Shin-nong-bon-cho-kyung.” Ginseng has diverse pharmacologic and therapeutic properties. Black ginseng (BG, Ginseng Radix nigra) is produced by repeatedly steaming fresh ginseng nine times. Studies of BG have shown that prolonged heat treatment enhances the antioxidant activity with increased radical scavenging activity. Several recent studies have showed the effects of BG on increased lipid profiles in mice. In this study report the effects of water and ethanol extracts of BG on hypercholesterolemia in rats. To our knowledge, this is the first time such an effect has been reported.

Methods

Experiments were conducted on male Sprague Dawley rats fed with a high-cholesterol diet supplemented with the water and ethanol extracts of BG (200 mg/kg). Their blood cholesterol levels, serum white blood cell levels, and cholesterol-metabolizing marker genes messenger RNA (mRNA) expression were determined. Liver and adipose tissues were histologically analyzed.

Results

We found that BG extracts efficiently reduced the total serum cholesterol levels, low-density lipoprotein (LDL) levels with increased food efficiency ratio and increased number of neutrophil cells. It also attenuated the key genes responsible for lipogenesis, that is, acetyl-coenzyme A (CoA) acetyltransferase 2, 3-hydroxy-3-methyl-glutaryl-CoA reductase, and sterol regulatory element-binding protein 2, at the mRNA level inside liver cells. Furthermore, the BG extract also reduced the accumulation of fat in adipose tissues, and inhibited the neutral fat content in liver cells stained with hematoxylin and eosin and oil red O.

Conclusion

Administration of BG extracts to Sprague Dawley rats fed with high-cholesterol diet ameliorated hypercholesterolemia, which was mediated via modulation of cholesterol-metabolizing marker genes. This data throw a light on BG's cardioprotective effects.