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Review Article Dendrobium officinale Kimura et Migo: A Review on Its Ethnopharmacology, Phytochemistry, Pharmacology, and Industrialization
Hanxiao Tang, Tianwen Zhao, Yunjie Sheng, Ting Zheng, Lingzhu Fu, and Yongsheng Zhang
Zhejiang Chinese Medical University, 548 Binwen Rd., Binjiang District, Hangzhou, China
Correspondence should be addressed to Yongsheng Zhang; [email protected]
Received 17 July 2016; Accepted 23 October 2016; Published 12 March 2017
Academic Editor: Hilal Zaid
Copyright © 2017 Hanxiao Tang et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Ethnopharmacological Relevance. Dendrobii Officinalis Caulis, the stems ofDendrobium officinaleKimura etMigo, as a tonic herb in Chinese materia medica and health food in folk, has been utilized for the treatment of yin-deficiency diseases for decades.Methods. Information for analysis ofDendrobium officinaleKimura etMigowas obtained from libraries and Internet scientific databases such as PubMed, Web of Science, Google Scholar, ScienceDirect, Wiley InterScience, Ingenta, Embase, CNKI, and PubChem. Results. Over the past decades, about 190 compounds have been isolated from Dendrobium officinale Kimura et Migo. Its wide modern pharmacological actions in hepatoprotective effect, anticancer effect, hypoglycemic effect, antifatigue effect, gastric ulcer protective effect, and so on were reported. This may mainly attribute to the major and bioactive components: polysaccharides. However, other small molecule components require further study. Conclusions. Due to the lack of systematic data of Dendrobium officinale, it is important to explore its ingredient-function relationships with modern pharmacology. Recently, studies on the chemical constituents of Dendrobium officinale concentrated in crude polysaccharides and its structure-activity relationships remain scant. Further research is required to determine theDendrobium officinale toxicological action and pharmacological mechanisms of other pure ingredients and crude extracts. In addition, investigation is needed for better quality control and novel drug or product development.
1. Introduction
Dendrobium officinale Kimura et Migo spreads in several countries over the world, such as Japan, United States, and Australia, and it distributes more widely in China [1] (Table 1). Modern pharmacology research has confirmed that Dendrobium officinale and its polysaccharide fraction pos- sess anticancer, hepatoprotective, hypolipidemic, antifatigue, antioxidant, anticonstipation, hypoglycemic, gastric ulcer protective, and antihypertensive effects, immunoenhance- ment, and so on [2–4].
Since 1994, polysaccharides of Dendrobium officinale have been extracted and analyzed [5], and polysaccharides gradually became research focus of Dendrobium officinale. Recently, the chemical compositions and pharmacological effects of Dendrobium officinale have attracted more and
more attention. In this review, from substantial data about Dendrobium officinale, approximately 190 monomer compo- sitions and plenty of pharmacological researches studied in vivo and/or in vitro were summarized. In addition, the devel- opment of artificial cultivation of Dendrobium officinale accelerates the promotion of its industrialization in China. Patents and health care products were also improved by the combination of production and research mode.
2. Pharmaceutical Botany
Dendrobium, pertaining to the second largest family, Orchi- daceae, includes approximately l,400 species worldwide dis- tributed from tropical Asia to Oceania [6]. There are 74 species and 2 variants of genus Dendrobium Sw. in China [7]. Some of them can be processed as Dendrobii Caulis
Hindawi Evidence-Based Complementary and Alternative Medicine Volume 2017, Article ID 7436259, 19 pages https://doi.org/10.1155/2017/7436259
https://doi.org/10.1155/2017/7436259
2 Evidence-Based Complementary and Alternative Medicine
Ta bl e 1: Th
et ax on
om ic cla
ss ifi ca tio
n, na m es ,a nd
di st rib
ut io n of
D en dr ob iu m
offi cin
al eK
im ur ae
tM ig o.
Sy no
ny m s
D en dr ob iu m
ca te na tu m
Li nd
l., G en .S p. O rc hi d. Pl .:
84 (1 83 0) .
D en dr ob iu m
str ick
la nd
ia nu
m Rc
hb .f. ,
G ar d. Ch
ro n. ,n
.s. ,7 :7 49
(1 87 7) .
Ca lli sta
str ick
la nd
ia na
(R ch b. f.)
Ku nt ze ,
Re vi s. G en .P
l. 2: 65 5 (1 89 1) .
D en dr ob iu m
to sa en se
M ak in o, J. Bo
t. 29 :3 83
(1 89 1) .
D en dr ob iu m
pe re -fa
ur iei
H ay at a, Ic on
.P l. Fo
rm os an .
6: 70
(19 16 ).
D en dr ob iu m
to sa en se
va r. pe re -fa
ur iei
(H ay at a)
M as am
., J.
So c. Tr op .A
gr ic .4 :1 96
(19 33 ).
D en dr ob iu m
offi cin
al e
Ki m ur a&
M ig o, J. Sh an gh
ai Sc i. In st.
3: 12 2 (19
36 ).
Ta xo no
m ic
cla ss ifi ca tio
n
Sp ec ie s2
00 0 & IT IS
Ca ta lo gu eo
fL ife :P
la nt ae >
Tr ac he op
hy ta > Li lio
ps id a>
A sp ar ag al es > O rc hi da ce ae
> D en dr ob
iu m >
D en dr ob iu m
ca te na tu m
Li nd
l.
IU CN
Re d Li st:
Pl an ta e>
Tr ac he op
hy ta > Li lio
ps id a
> O rc hi da le s>
O rc hi da ce ae >
D en dr ob
iu m >
D en dr ob iu m
offi cin
al e
N CB
IT ax on
om y: Eu
ka ry ot a>
Vi rid
ip la nt ae
> St re pt op
hy ta > St re pt op
hy tin
a> Em
br yo ph
yt a>
Tr ac he op
hy ta >
Eu ph
yl lo ph
yt a>
Sp er m at op
hy ta >
M ag no
lio ph
yt a>
M es an gi os pe rm
ae >
Li lio
ps id a>
Pe tro
sa vi id ae > A sp ar ag al es >
O rc hi da ce ae > Ep
id en dr oi de ae >
Ep id en dr oi de ae
in ce rt ae
se di s>
D en dr ob
iin ae > D en dr ob
iu m > D en dr ob iu m
ca te na tu m
Ta xo no
m ic H ie ra rc hy
of CO
L- Ch
in a2
01 2: Pl an ta e>
A ng
io sp er m ae >
M on
oc ot yl ed on
ea e>
M ic ro sp er m ae >
O rc hi da ce ae > D en dr ob
iu m
> D en dr ob iu m
to sa en se
Tr op
ic os
re so ur ce :
Eq ui se to ps id aC
.A ga rd h >
A sp ar ag al es
Li nk >
O rc hi da ce ae
Ju ss .>
Ca lli sta
Lo ur .>
Ca lli sta
str ick
la nd
ia na
Ku nt ze
Tr op
ic os
re so ur ce :
Eq ui se to ps id aC
.A ga rd h > A sp ar ag al es
Li nk >
O rc hi da ce ae
Ju ss .>
D e n dr ob
iu m
Sw .>
D en dr ob iu m
offi cin
al eK
im ur a&
M ig o
D ist rib
ut io n
Ja pa n > Ky
us hu
U ni te d St at es > M iss ou
ri > Sa in tL
ou is Ci ty
Au str
al ia > N ew
So ut h W al es
Ch in a>
Ta iw an ,A
nh ui ,Z
he jia ng
,F uj ia n, G ua ng
xi ,
Si ch ua n,
Yu nn
an ,X
iz an g, et c.
C om
m on
na m e
鐵 皮 石 斛
(ti ep ish
ih u)
黃 石 斛
(h ua
ng sh ih u)
Re fe re nc e
ht tp :// w w w. ke w. or g/
ht tp :// w w w. th ep la nt lis t.o
rg /
ht tp :// w w w. ca ta lo gu
eo fli fe .o rg /
ht tp :// w w w. tro
pi co s.o
rg /
ht tp :// w w w. gb if. or g/
ht tp :// w w w. eo l.o rg /
ht tp :// fr ps .efl
or a.c
n/ [5 0]
[5 1]
[1 0]
http://www.kew.org/ http://www.theplantlist.org/ http://www.catalogueoflife.org/ http://www.tropicos.org/ http://www.gbif.org/ http://www.eol.org/ http://frps.eflora.cn/
Evidence-Based Complementary and Alternative Medicine 3
(a) (b)
Figure 1: (a) Dendrobium officinale Kimura et Migo; (b) tiepifengdou.
(Chinese:石斛, shihu) of Chinesemateriamedica [8]. In 2005 Chinese Pharmacopoeia (ChP), tiepishihu (Chinese:鐵皮石 斛) was one species of medicinal shihu called Dendrobium candidum Wall. ex Lindl. [9]; however this Latin name was later disputed and considered the synonym of Dendrobium moniliforme (L.) Sw. [10, 11]. In 2010 ChP, tiepishihu was ren- amed as Dendrobium officinale Kimura et Migo (aka Den- drobium officinale, Figure 1(a)). This Latin name was firstly denominated by two Japanese scholars in 1936 when they found the new species of Dendrobium in China [12]. Facil- itating the preservation, the fibrous stems of Dendrobium officinale can