General

Scientific Names: Magnolia denudata Desr.

Common Names: Yu Lan, Xin Yi, Mu Lan, Yu Lan Hua, Bai Yu Lan, Ying Chun Hua, Yu Tang Chun.


BOTANICAL:

玉兰 (Magnolia)

中药材基原: 为木兰科植物玉兰Magnolia denudata Desr. 的花蕾。

植物形态: 落叶乔木,高达15m。嫩枝有毛,冬芽密生灰绿色长绒毛。叶互生,倒卵形至倒卵状矩圆形,长10~18cm,宽6~10cm,先端阔而突尖,基部渐狭,全缘,上面有光泽,下面被柔毛。花大,钟形,先叶开放;花被片9,3轮,白色,矩圆状倒卵形;雄蕊、心皮多数,分别螺旋状排列于伸长的花托上,骨朵果顶端圆形,多数,聚合成圆筒形。花期2~3月。果期6~7月。

资源分布: 分布河南、山东、江苏、浙江、安徽、江西、福建、广东、广西、四川、云南、贵州、陕西等地。药材全国大部分地区有产,主产河南、四川、安徽、 浙江、陕西、湖北等地。

生药材鉴定:干燥的花蕾,呈倒圆锥状,形如毛笔 头,基部带有木质短枝。花蕾长1~4厘米,中部直径0.7~2厘米。外裹苞片2枚成两层,两 层之间尚可见小芽鳞。苞片表面密被黄绿色柔软长毛,毛茸长约5毫米,内表面平滑,棕紫色。 除去苞片后可见3片花萼与6~9~12 片紧密相包的棕紫色花瓣,其内有多数棕黄色雄蕊与1枚褐色雌蕊。质脆易破碎。有特殊香气,味辛凉而稍苦。以花蕾未开,身干,色绿,无枝梗 者为佳。

 

 

Pharmacology

化学成分: 玉兰花蕾含挥发油,中含柠檬醛、丁香油酚、 1,8一桉叶素(Cineole)。根含木兰花碱(Magnoflorine)。叶和果实都含芍药素(Paeonidin)的甙。 从望春花花蕾中提出一种生物碱结晶(C17 H19 O3 N,熔点 208℃)。另还分出松树脂醇二甲醚(Eudesmin)、鹅掌楸 树脂醇B二甲醚(Lirioresinol B dimethyl ether)、望春 花素(Magnolin)和发氏玉兰素(Fargesin)等木脂体 (Lignans)成分。(1)望春玉兰 花蕾含挥发油2.86%,油中主要成分为α-松油二环烯、桉油精、胡椒酚甲醚和枸橼醛等,后三者是辛味成分。另报道同其花蕾中分离出 4种木脂素类成分,为冷杉脂酚二甲醚(pinoresinol dimethyl ether)鹅掌楸脂醇-β-二甲醚(lirilresinol dimethyl ether)、木兰木脂体(magnolin)和辛夷木脂体(fargesin)。还分得一有毒酚性生物碱(C17H19O3N,熔点208℃)。(2)玉兰花蕾含挥发油,油中含枸橼醛(citral)、丁香油酚(eugenol)、桉油精(cineole)。(3)武当玉兰 花蕾含挥发油从中检出40个组分,鉴定了其中32个成分,会计师在 5%以上的有乙酸龙脑脂(bornyl acetate)、反-丁香烯(trans-caryophyllene)、环氧丁香烯(caryophylleneoxide)和β-桉油醇(β-eudesmol)。

 

 

Efficacy

IN VITRO:

  1. Ha KT, et al., Inhibitory effect of Daesungki-Tang on the invasiveness potential of hepatocellular carcinoma through inhibition of matrix metalloproteinase-2 and -9 activities. Toxicol Appl Pharmacol. 2004 Oct 1; 200(1):1-6.
  2. Bai X, et al., Honokiol, a small molecular weight natural product, inhibits angiogenesis in vitro and tumor growth in vivo. J Biol Chem. 2003 Sep 12; 278(37):35501-7. Epub 2003 Jun 19.
  3. Yang SE, et al., Effector mechanism of magnolol-induced apoptosis in human lung squamous carcinoma CH27 cells. Br J Pharmacol. 2003 Jan; 138(1):193-201.
  4. Choi JH, et al., Costunolide triggers apoptosis in human leukemia U937 cells by depleting intracellular thiols. Jpn J Cancer Res. 2002 Dec; 93(12):1327-33.
  5. Yang SE, et al., Down-modulation of Bcl-XL, release of cytochrome c and sequential activation of caspases during honokiol-induced apoptosis in human squamous lung cancer CH27 cells. Biochem Pharmacol. 2002 May 1; 63(9):1641-51.
  6. Lin SY, et al., Magnolol suppresses proliferation of cultured human colon and liver cancer cells by inhibiting DNA synthesis and activating apoptosis. J Cell Biochem. 2002; 84(3):532-44.
  7. Nagase H, et al., Inhibitory effect of magnolol and honokiol from Magnolia obovata on human fibrosarcoma HT-1080. Invasiveness in vitro. Planta Med. 2001 Nov; 67(8):705-8.
  8. Konoshima T, et al., Studies on inhibitors of skin tumor promotion, IX. Neolignans from Magnolia officinalis. J Nat Prod. 1991 May-Jun; 54(3):816-22.
  9. Wiedhopf RM, et al., Tumor inhibitory agent from Magnolia grandiflora (Magnoliaceae). I. Parthenolide. J Pharm Sci. 1973 Feb; 62(2):345.

IN VIVO:

  1. Ikeda K, et al., Inhibitory effect of magnolol on tumour metastasis in mice. Phytother Res. 2003 Sep; 17(8):933-7.
  2. Bai X, et al., Honokiol, a small molecular weight natural product, inhibits angiogenesis in vitro and tumor growth in vivo. J Biol Chem. 2003 Sep 12; 278(37):35501-7. Epub 2003 Jun 19.

 

 

Safety

用药忌宜:阴虚火旺者忌服。《本草经疏》:“凡气虚人忌,头脑痛属血虚火炽者忌,齿痛属胃火者忌。《本草汇言》:“气虚之人,虽偶感风寒,致诸窍不通者, 不宜用。”

 

 
   
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