Poria cocos is a fungus widely used as a Chinese traditional herbal medicine for centuries. Poria Cocos is known in China as Fu LIng. Little western research has been done with this herb.
See Chinese Herbs for a list of herbs used in Chinese Medicine. Historically Poria Cocos has been used as a sedative and diuretic.
Potential benefits of Poria Cocos
One lab study indicates Poria Cocos has anti-leukemia activity. Another
shows Poria Cocos has anti-inflammatory activity that may be useful in
inflammatory skin conditions such as
psoriasis. Poria
cocos hay have anti-tumor potential, for instance against sarcoma. Human
studies in the West are lacking, therefore it is difficult to say what the
clinical role of poria cocos is in human health and disease.
Rehmannia Endurance, 637 mg, 150
Tabs - With Poria Cocos
Planetary Formulas

Planetary Formulas Rehmannia Endurance is based on the classic Chinese tonifer
Rehmannia Six: Liu Wei Di Huang Wan, one of the most strengthening tonics of
Chinese herbalism. Traditionally it was used for those who are tired and run
down from overwork and inadequate rest due to a fast paced-lifestyle.
Rehmannia Supplement Facts:
Calcium
Rehmannia Root
Poria Cocos Sclerotium
Tree Peony Root Bark
Dioscorea Root
Alisma Rhizome
He Shou Wu Root (Fo Ti)
Chrysanthemum
Flower
Ligustrum Seed
Saw Palmetto Berry
Lycii Fruit Extract
Cornus Fruit
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Research Update newsletter. Twice a month we email a brief abstract
of several studies on various supplements and natural medicine topics, including
poria cocos, and their practical interpretation by Ray Sahelian, M.D.
What's in Poria Cocos?
Numerous compounds are found in this fungus including triterpenes, turmerone, ergosterol peroxide, polyporenic acid C, dehydropachymic acid, pachymic acid, tumulosic
acid, heteropolysaccharides, and many others.
Poria Cocos Research Update
Antioxidant activities of some common ingredients of traditional chinese
medicine, Angelica sinensis, Lycium barbarum and Poria cocos.
Phytother Res. 2004 Dec;18(12):1008-12.
The antioxidant activities of three popular ingredients of traditional Chinese
medicine, namely Angelica sinensis (AS), Lycium barbarum (LB) and Poria cocos
were evaluated in this study. The results showed that aqueous extracts of these
crude drugs exhibited antioxidant activities in a concentration-dependent
manner. All extracts displayed an inhibitory effect on FeCl2-ascorbic acid
induced lipid peroxidation in rat liver homogenate in vitro, with the order of
activity LB > AS > Poria cocos. The present study concludes that LB extract possessed the strongest
inhibition on malondialdehyde formation in rat liver homogenate, and superoxide
anion scavenging and anti-superoxide formation activities. These results also
suggest that LB extract is a good source of antioxidant agent in the daily
dietary supplement.
Cytotoxicity and DNA topoisomerases inhibitory activity of constituents
from the sclerotium of Poria cocos.
Arch Pharm Res. 2004 Aug;27(8):829-33.
The bioactivity-guided fractionation of the methylene chloride extract of the
sclerotium of Poria cocos led to the isolation of (S)-(+)-turmerone (1),
ergosterol peroxide (2), polyporenic acid C (3), dehydropachymic acid (4),
pachymic acid (5), and tumulosic acid (6). Compounds 4-6 exhibited moderate
cytotoxicities, with IC50 values of 20.5, 29.1, and 10.4 microM, respectively,
against a human colon carcinoma cell line. However, 3-6 not only showed
inhibitory activities as potent as etoposide used as a positive control on DNA
topoisomerase II (36.1, 36.2, 43.9 and 66.7% inhibition at a concentration of 20
microM, respectively), but also inhibition of DNA topoisomerase I (55.8, 60.7,
43.5, and 83.3% inhibition at a concentration of 100 microM, respectively).
Antiproliferative and differentiating effects of polysaccharide fraction
from fu-ling (Poria cocos) on human leukemic U937 and HL-60 cells.
Food Chem Toxicol. 2004 May;42(5):759-69.
Poria cocos, Fu-Ling, is an oriental fungus and has been widely used as a
Chinese traditional herbal medicine for centuries. In the present study, a
neutral polysaccharide fraction from Poria cocos was isolated by a series of
chromatographies and its effects on antiproliferation and differentiation of
human leukemic cells, U937 and HL-60, were investigated in vitro. Results showed
that the molecular weight of isolated Poria cocos was approximately 160
kDa, as estimated by gel permeation chromatography. It suggests that Poria cocos
is a biological response modifier (BRM), instead of a cytotoxic reagent, and may
be a potential alternative in leukemia therapy.
Dehydrotrametenonic acid and dehydroeburiconic acid from Poria cocos and
their inhibitory effects on eukaryotic DNA polymerase alpha and beta.
Biosci Biotechnol Biochem. 2004 Feb;68(2):448-50.
A new lanostane-type triterpene acid,
(20xi)-3-oxolanosta-7,9(11),24-trien-21-oic acid (1; dehydrotrametenonic acid),
along with a known triterpene acid, dehydroeburiconic acid (2), were isolated
from the epidermis of the sclerotia of Poria cocos. The structure of 1 was
analyzed on the basis of spectroscopic methods. Compounds 1 and 2 inhibited calf
DNA polymerase alpha and rat DNA polymerase beta.
Influence of traditional Chinese
anti-inflammatory medicinal plants on leukocyte and platelet functions. Pharm Pharmacol. 2003 Sep;55(9):1275-82.
The enzymes 5-lipoxygenase and elastase are therapeutic targets in
dermatological disorders such as psoriasis. Fifteen extracts from
traditional Chinese medicinal plants used to treat topical inflammations
were screened for their inhibitory effect on lipoxygenase, cyclooxygenase
and elastase activity in intact leukocytes and platelets. Astragalus
membranaceus, Forsythia suspensa and Poria cocos inhibited 5-lipoxygenase,
with IC50 values of 141, 80 and 141 microg mL(-1), respectively. The
latter two species, along with Angelica dahurica and Angelica pubescens,
also inhibited elastase, while Angelica pubescens, Atractylodes macrocephala, Lentinus
edodes, Rehmannia glutinosa and Paeonia lactiflora selectively inhibited
12-(S)-HHTrE production, a valid marker of cyclooxygenase activity. The
inhibition of phospholipase A(2) activity by Poria cocos is discussed.
Dehydrotumulosic and pachymic acids, which have been isolated from Poria cocos, were shown to inhibit leukotriene
B(4) release. The results indicate that both Poria cocos and Forsythia suspensa are potentially valuable
species in the management of skin pathologies involving chronic
inflammation.
Antitumor activities of heteropolysaccharides of Poria cocos mycelia from
different strains and culture media.
Carbohydr Res. 2003 Jul 4;338(14):1517-21.
Ten water-soluble heteropolysaccharide fractions were isolated from Poria
cocos mycelia cultured from one wild and one cultivated strain in two identical
culture media differing only in one component: either corn steep liquor or bran
extract. The chemical compositions, including monosaccharide profile, protein
content, and molecular mass M(w) of the mycelial polysaccharides were
determined. Both the in vitro and in vivo antitumor activities of the
heteropolysaccharides were evaluated and compared. The heteropolysaccharides
from Poria cocos mycelia cultured with the wild strain in a medium containing
corn steep liquor exhibited the highest antitumor activities against Sarcoma 180
in vivo.
Inhibitory effects of triterpenes isolated from Hoelen on free
radical-induced lysis of red blood cells.
Phytother Res. 2003 Feb;17(2):160-2.
Hoelen, sclederma of Poria cocos Wolf, has long been used as a sedative and
diuretic in traditional medicine. Formerly, we demonstrated that Hoelen in vitro
protects red blood cells from AAPH-induced hemolysis. In this study, tests were
carried out to identify the main ingredient of Hoelen that has the scavenging
effect on free-radicals. Triterpene carboxylic acids isolated from the methanol
extract of Hoelen, i.e. pachymic acid, polyporenic acid, 3-epidehydrotumulosic
acid, 3beta-hydroxylanosta-7,9(11), 24-trien-21-oic acid and 3-o-acetyl-16 alpha
-hydroxytrametenolic acid, were found to have inhibitory activities against AAPH-induced
lysis of red blood cells.
[Effects of poria cocos on ototoxicity induced by kanamycin in
guinea-pigs]
Zhongguo Zhong Xi Yi Jie He Za Zhi. 1995 Jul;15(7):422-3.
In order to prevent the ototoxicity of kanamycin (KM), the effects of Poria
Cocos on the ototoxicity induced by KM in guinea-pigs was observed by infusing
the Poria Cocos-decoction into the guinea-pigs with comparing the difference in
the general intoxicating symptom, prayer's reflex (PR) threshold, brainstem
auditory evoked potentials (BAEPs) and the absence rate of outer hair cells in
the first turn of cochlea. The results suggested that the ototoxicity of KM was
retarded by giving the Poria Cocos decoction. The results suggested that Poria
Cocos might be antagonistic to the ototoxicity of KM in guinea-pigs.
Hoelen (Poria Cocos Wolf) and ginseng (Panax Ginseng C. A. Meyer), the
ingredients of a Chinese prescription DX-9386, individually promote hippocampal
long-term potentiation in vivo.
Biol Pharm Bull. 1995 Apr;18(4):518-22.
DX-9386 is a traditional Chinese medicinal prescription consisting of ginseng
(Panax Ginseng C. A. Meyer), polygala (Polygala Tenuifolia Willdenew), acorus (Acorus
Gramineus Soland) and hoelen (Poria Cocos Wolf). We recently found that oral
administration of the prescription at a dose of 500 mg/kg intensified the
formation of long-term potentiation (LTP) in the dentoff gyrus of anesthetized
rats. To evaluate the individual contribution of separate ingredients in DX-9386
towards the observed biological activity, we investigated their direct influence
upon LTP formation in vivo. A single oral administration of hoelen and ginseng
(250 and 500 mg/kg) significantly increased the spike amplitude evoked by a
subthreshold tetanic stimulation at time intervals up to 30 min after tetanus.
Only minor effects of polygala (500 mg/kg) and no influence of acorus up to 500
mg/kg were observed. No drugs affected the basal spike amplitude induced by a
test stimulus. In addition, we ascertained that DX-9386 was also active at a
dose of 250 mg/kg. Taken together, these results indicate that hoelen and
ginseng are the active components of DX-9386 with regard to the enhancement of
hippocampal LTP.
[Studies on chemical constituents from solvent extracts of Poria cocos (Schw.)
Wolf]
Zhongguo Zhong Yao Za Zhi. 1993 Oct;18(10):613-4, 639.
Crystals I-N were isolated from the ethereal extracts of Poria cocos and
identified respectively as O-acetyl-pachymic acid (I), 3
beta-hydroxy-lanosta-7,9(11),24-trien-21-oic acid (II), beta-amyrin acetate
(III) and 3 beta-hydroxy-16 alpha-acetoxy-lanosta-7,9(11),24-trien-21-oic acid
(N). Crystal III was obtained from P. cocos for the first time, and crystal N
was newly discovered.
Suppression of tumor necrosis factor-alpha, interleukin-1 beta,
interleukin-6 and granulocyte-monocyte colony stimulating factor secretion from
human monocytes by an extract of Poria cocos.
Zhonghua Min Guo Wei Sheng Wu Ji Mian Yi Xue Za Zhi. 1992 Feb;25(1):1-11.
Fu-Ling, the sclederma of Poria cocos (Schw.) Wolf, has long been used as a
sedative and diuretic. However, data in this report suggest that Fu-Ling is a
potential suppressor of cytokine secretion from human peripheral blood monocytes
under in vitro condition. Monocyte culture medium containing 10% of Fu-Ling
extract significantly inhibited secretion of TNF-alpha, IL-beta, IL-6 and GM-CSF
from the monocyte monolayer. However, as Fu-Ling extract content was gradually
reduced, cytokine secretion was augmented in comparison with the cytokine
secretion in drug-free controls. This augmentative effect resulted from the
trace amount (1.24 ng/ml in 0.62% of Fu-Ling extract) of lipopolysaccharide
(LPS) which contaminated the Fu-Ling extract during the preparation process,
since TNF-alpha, IL-1 beta and IL-6 secretion induced by 0.62% Fu-Ling extract
could be significantly inhibited by polymyxin B, an LPS inhibitor. Furthermore,
the amounts of TNF-alpha IL-1 beta and IL-6 induced by 1 ng/ml of LPS without
the presence of drug were more than that induced by 0.62% of Fu-Ling extract.
Thus, cytokine secretion induced by LPS contamination (1.24 ng/ml) in the
Fu-Ling extract was partially suppressed by 0.62% of the Fu-Ling extract itself.
GM-CSF secretion in the medium containing 0.62% of Fu-Ling extract was not
induced by LPS since: a) GM-CSF induced by 0.62% Fu-Ling extract could not be
inhibited by polymyxin B; b) LPS at 1 ng/ml showed no activity indicating
induction of GM-CSF secretion.
Poria Cocos Emails
Dear Dr. Sahelian and staff, I have purchased several supplements from
Physicianformulas.com in the
past on behalf of a prostate cancer patient friend, and he and I are extremely
pleased with the quality and dependability of the services and products, and
thorough information available on your website. I
hope you may find the time to inform me about the availability and suitability
of a combination of supplements I am currently seeking for my mother (in
Belgium), 82, who is suffering from communicative
hydrocephalus and will get a lumbar punction for temporary alleviation of her
symptoms (triad: intermittent dementia episodes, ataxia and urinary
incontinence). She is also a heart patient on coumadin, mild postassium-sparing
diuretic Burinex, atenolol and supportive aspirin (2 yr post mural infarct, and
chronic atrial fibrillation). She would not be a good candidate for placement of
a CSF drainage shunt due to her advanced age and medical complications, and the
risks involved in this surgical intervention (anesthesia complications, risk of
infection, occlusion or shunt malfunction with need for repeated surgical
intervention, and of course risk for subdural hematoma). Her neurologist agreed
to a long-term physical therapy including Bruno Chikly's lymph drainage
treatment method after she recovers from the
lumbar punction, but he was not very hopeful about long-term alleviation of her
symptoms. I have done some online research about availability of supplements to
treat communicative hydrocephalus, and I have found a couple of links to Chinese
Herb therapy sites, located in the Orient, and offering supplements that contain
rather unusual components (dried earth worms? Lumbricus) and may not be subject
to the same quality control as the products that Physician formulas may be
offering. I have serious reservations about ordering Chinese "herbs" without the
proper quality control, as there have been several lethal incidents in Europe
involving cardiac, kidney and liver complications after usage of non-controlled
Oriental supplements. Sofar I have not been successful in locating any other
supplements except for your formula.I have found your supplement containing
poria cocos and alisma rhizome. This supplement also contains several other
herbs, among which Dioscorea which may occasionally have undesirable
gastro-intestinal side effects. I have yet to familiarize myself with the
pharmacological actions of Fo Ti, but the other components definitely seem so
complement the formula. I am very inclined to order this formula if there
are no increased cardiac, liver or kidney toxicity damage risks associated with
the normal use of this supplement. My sincere apologies in advance, I know I
should be able to do some research myself
to evaluate these components, but I am convinced that Physician Formulas has all
the quality control and side effect issues on file for this supplement, so it
seemed like the most logical thing to do, i.e. ask you
about any possible side effects we may have to be aware of. I am very grateful
for your advice in this matter, and I hope that you may judge the Poria cocos
supplement to be a safe supplement for my mom
to try.
A. Thank you so much for your email. I does not feel
there is enough research with this product to be comfortable for its safety in a
complicated case as the one you present. Some herbs in this product could have
cardiac stimulating properties that could lead to arrhythmia in a fragile
patient. So, at this time, this is probably not a recommended product. Take care
and we wish the best, we really can't say much more since it is such a
complicated case.
Poria Cocos questions
Q. Does porio cocos help with
sleep?
A. I have not tried poria cocos personally to know whether it is a
good sedative. I find Good Night Rx to be quite helpful.