References
[1] Barefoot Doctor's Manual- 1977 Prepared by the Revolutionary Health Committee
of Hunan Province. Original Chinese manual- Victor W. Sidel. Originally published
by Dr Joseph Quin and the Fogarty International centre, Bethdesda (1974). Madrona
Publishers Seattle Washington ISBN 0-914842-52-8
[2] A Complete English Dictionary of Medicinal Terms in Chinese Acupuncture
and Herbalism 1981- Henry Lu Chinese Foundations of Natural Health- The Academy
of Oriental Heritage, Vancouver, Canada.
[3] Medicated Diet of Traditional Chinese Medicine- Chief Editor- Hou Jinglun.
Associate Editors- Zhao Xin, Li Weidong, Liu Jianxin, Geng Chun-e, Li Guohua,
Li Shaohua. Geijing. Science & Technology Press 1994. ISBN 7-5304-1735-5/R.
309.
[4] Translation notes from Gary Seiford and Hocu Huhn- NSW College of Natural
Therapies. Sydney Australia (1982).
[5]
Inner Path
[6] Pharmacology and Applications of Chinese Materia Medica Vol 1, Ed. H.
Chan and P. But, Pub. World Scientific (1986) Singapore
[7] Xu, S.X. (1986) Chung Yao Tung Pao 11 (2),42
Images
1.
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2.
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Inner Path can not take any responsibility for any adverse effects from
the use of plants. Always seek advice from a professional before using a plant
medicinally.
Constituents.
Dihydroflavones; Carthamone, a benzoquinone
pigment, together with carthamin and neocarthamin.[1]
Lignans; tetracheloside, matairesinoside and 2-hydroxyartiin.
A polysaccarhide composed of xylose, fructose, galactose, glucose, arabinose,
rhamnose and uronic acid residues.
References
[1] Pharmacology and Applications of Chinese Matria Medica Vol 1, Ed. H. Chan
and P. But, Pub. World Scientific (1986) Singapore
[2] Naturally Occurring Quinones, R.H. Thomson, 2nd Ed. Pub. Academic Press
(1971)
[3] The Chemistry of Lignans, Ed. C.B.S. Rao, Pub. Andhra University Press
(1978) Andhra Pradesh, India
[4] Caldes, G. et al. (1981) J. Gen. Appl. Microbiol. 27, 157
Research.
The polysaccaride induces antibody formation in mice following peritoneal injection;
these antibodyes cross react with antisera specific for
Streptococcus pneumoniae
type III and type VIII.
[1]
Extracts have also been tested on blood coagulation, where a prolongation of
clotting time was observed and platelet aggregation inhibited. Other properties
include an increase in the tolerance of mice to hypoxia and a stimulant effect
on the uterus, particularly the pregnant uterus, in animals. Clinically Safflower
is used in China to treat coranary disease, thrombotic disorders and menstrual
disturbances and alcholic extract are applied topically to ulcers and wounds.
[2]
References
[1] Caldes, G.
et al. (1981) J. Gen. Appl. Microbiol. 27, 157
[2] Pharmacology and Applications of Chinese Matria Medica Vol 1, Ed. H. Chan
and P. But, Pub. World Scientific (1986) Singapore
Phytochemistry, pharmacology and medicinal properties of Carthamus tinctorius
L.
Asgarpanah J, Kazemivash N.
Abstract
Carthamus tinctorius L. is commonly known as Safflower. C. tinctorius extracts
and oil are important in drug development with numerous pharmacological activities
in the world. This plant is cultivated mainly for its seed, which is used as
edible oil. For a long time C. tinctorius has been used in traditional medicines
as a purgative, analgesic, antipyretic and an antidote to poisoning. It is a
useful plant in painful menstrual problems, post-partum hemorrhage and osteoporosis.
C. tinctorius has recently been shown to have antioxidant, analgesic, anti-inflammatory
and antidiabetic activities. Carthamin, safflower yellow are the main constituents
in the flower of C. tinctorius. Carthamidin, isocarthamidin, hydroxysafflor
yellow A, safflor yellow A, safflamin C and luteolin are the main constituents
which are reported from this plant. Caryophyllene, p-allyltoluene, 1-acetoxytetralin
and heneicosane were identified as the major components for C. tinctorius flowers
essential oil. Due to the easy collection of the plant and being widespread
and also remarkable biological activities, this plant has become both food and
medicine in many parts of the world. This review presents comprehensive analyzed
information on the botanical, chemical and pharmacological aspects of C. tinctorius.
PMID: 23371463 DOI: 10.1007/s11655-013-1354-5 |Chin J Integr Med. 2013 Feb;19(2):153-9.
doi: 10.1007/s11655-013-1354-5. Epub 2013 Jan 31.
ncbi.nlm.nih.gov
Antioxidative compounds isolated from safflower (Carthamus tinctorius
L.) oil cake.
Zhang HL, Nagatsu A, Watanabe T, Sakakibara J, Okuyama H.
Abstract
Seven antioxidative serotonin derivatives were isolated from safflower (Carthamus
tinctorius L.) oil cake. Their structures were established as N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]ferulamide
(1), N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]-p-coumaramide (2), N,N'-[2,2'-(5,5'-dihydroxy-4,4'-bi-1H-indol-3,3'-yl)diethyl]-
di-p-coumaramide (3), N-[2-[3'-[2-(p-coumaramido)ethyl]-5,5'-dihydroxy- 4,4'-bi-1H-indol-3-yl]ethyl]ferulamide
(4), and N,N'-[2,2'-(5,5'-dihydroxy-4,4'-bi-1H-indol-3,3'-yl)diethyl]- diferulamide
(5), N-[2-[5-(beta-D-glucosyloxy)-1H-indol-3-yl)ethyl]- p-coumaramide (6), and
N-[2-[5-(beta-D-glucosyloxy)-1H-indol-3-yl)ethyl]ferulamide (7). Antioxidative
activities of the compounds were measured by the ferric thiocyanate method and
the alpha,alpha-diphenyl-beta-picrylhydrazyl (DPPH) method, and compounds 1-5
were found to have relatively strong antioxidative activity.
PMID: 9433760 Chem Pharm Bull (Tokyo). 1997 Dec;45(12):1910-4.
ncbi.nlm.nih.gov
Hair growth-promoting effect of Carthamus tinctorius floret extract.
Junlatat J, Sripanidkulchai B.
Abstract
The florets of Carthamus tinctorius L. have traditionally been used for hair
growth promotion. This study aimed to examine the potential of hydroxysafflor
yellow A-rich C. tinctorius extract (CTE) on hair growth both in vitro and in
vivo. The effect of CTE on cell proliferation and hair growth-associated gene
expression in dermal papilla cells and keratinocytes (HaCaT) was determined.
In addition, hair follicles from mouse neonates were isolated and cultured in
media supplemented with CTE. Moreover, CTE was applied topically on the hair-shaved
skin of female C57BL/6 mice, and the histological profile of the skin was investigated.
C. tinctorius floret ethanolic extract promoted the proliferation of both dermal
papilla cells and HaCaT and significantly stimulated hair growth-promoting genes,
including vascular endothelial growth factor and keratinocyte growth factor.
In contrast, CTE suppressed the expression of transforming growth factor-β1
that is the hair loss-related gene. Furthermore, CTE treatment resulted in a
significant increase in the length of cultured hair follicles and stimulated
the growth of hair with local effects in mice. The results provided the preclinical
data to support the potential use of CTE as a hair growth-promoting agent.
PMID: 24338940 DOI: 10.1002/ptr.5100 Phytother Res. 2014 Jul;28(7):1030-6. doi:
10.1002/ptr.5100. Epub 2013 Dec 11.
ncbi.nlm.nih.gov
Potent α-glucosidase inhibitors from safflower (Carthamus tinctorius
L.) seed.
Takahashi T, Miyazawa M.
Abstract
As part of the search for naturally derived α-glucosidase inhibitors, the chemical
components isolated from safflower seed (Carthamus tinctorius L.) were evaluated.
The compounds active as α-glucosidase inhibitors were serotonin derivatives
(e.g. N-p-coumaroyl serotonin (1) and N-feruloyl serotonin (2)). These compounds
showed a potent inhibitory activity, the 50% inhibitory concentration (IC(50)
) values were calculated as 47.2 µm (1) and 99.8 µm (2) while that of the reference
drugs acarbose and 1-deoxynojirimycin were evaluated as 907.5 µm and 278.0 µm,
respectively. Regarding the structure of the serotonin derivative, the existence
of the hydroxyl group at 5-position in the serotonin moiety and the linkage
of cinnamic acid and serotonin are essential for α-glucosidase inhibitory activities.
These results are helpful for the proper use of safflower seed as traditional
medicine for the treatment of diabetes, moreover, it could serve to develop
medicinal preparations as supplements and functional foods for diabetes. In
particular, the serotonin compounds could be used as a lead compound for a new
potential α-glucosidase inhibitor derived from the plant.
PMID: 22021176 DOI: 10.1002/ptr.3622 Phytother Res. 2012 May;26(5):722-6. doi:
10.1002/ptr.3622. Epub 2011 Oct 24.
ncbi.nlm.nih.gov