HOPS plant by
Ray Sahelian, M.D. Does Hops plant help
with sleep?
Hops plant
(Humulus lupulus) is a native British plant with a stout root,
heart-shaped leaves and cone-like flowers. Romans ate the young hops plant shoots in the
spring in the same way we do asparagus. Hops plant was first used by breweries in the
Netherlands in the early fourteenth century to make beer. Hops has been used traditionally
for nervous disorders and to help
anxiety or
sleep. Good Night Rx is an
all natural and effective herbal product for sleep.
Nature's Way Hops Flowers, 310 mg
Good Night Rx with hops plant extract for deeper sleep, formulated by Ray
Sahelian, M.D.

Hops
Supplement Facts:
Hops (flower)
Click here to buy Hops flowers supplement, to buy Good Night Rx herbal formula
with hops for deeper sleep, or to subscribe to a FREE newsletter
Recommendations for hops supplement: Take 1 or 2 hops capsules in the evening. The hops capsules may be opened
and placed in a cup with hot water for tea, and lightly sweetened with stevia.
* Hops daily value not established
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Research Update newsletter. Twice a month you will receive an email
discussing several new studies on various supplements and
alternative medicine topics,
including hops, and their practical interpretation
by Ray Sahelian, M.D. We will discuss research on hops plant as it becomes available.
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Hops plant benefits
Hops is useful as a sleep inducer, has antioxidant activity,
anti-inflammatory, estrogen-like
properties, and potential anti-tumor activity. Furthermore, compounds in hops
may reduce insulin resistance. Additional nutrients helpful for sleep include
melatonin and
tryptophan.
5HTP is a nutrient that helps
with relaxation.
Passion Flower and
kava are
herbs that help
to calm nerves.
Hops and Cancer
Extracts of several estrogenic herbs, including hops, black cohosh and vitex,
inhibit growth of breast cancer cells. These in vitro results suggest that certain herbs
and phytoestrogens may have potential in the prevention of breast cancer.
Six flavonoids from hops (Humulus lupulus) were tested for their antiproliferative
activity in human breast cancer (MCF-7),
colon cancer (HT-29) and ovarian cancer. All the
hop flavonoids were cytotoxic (cell killing) in the three cell lines. As antiproliferative agents,
chalcone and its (flavanone isomer may have potential chemopreventive activity against
breast and ovarian cancer in humans.
A potent phytoestrogen in hops, 8-prenylnaringenin, has an activity greater than other
established plant estrogens. The estrogenic activity of this compound was reflected in its
relative binding affinity to estrogen receptors from rat uteri. The presence of
8-prenylnaringenin in hops may provide an explanation for the accounts of menstrual
disturbances in female hop workers. This phytoestrogen can also be detected in beer, but
the levels are low and should not pose any cause for concern.
When to take hops plant supplement
Due to its sedative effects, hops is best reserved for evening or nighttime.
Hops as an anti-inflammatory
An interesting study listed below discusses the ability of compounds in
hops plant to act as COX-2 inhibitors just like some of the new
arthritis drugs Vioxx
and Celebrex which may make hops plant a potential therapy in cases of arthritis.
Hops and beer
The first mention of hops being used in beer was in 1067 by Abbes Hildegard of
Bingen so hops were likely used pretty widely before then.
Hops Research Update
Comparison of the in vitro estrogenic activities of
compounds from hops plant (Humulus lupulus) and red clover (Trifolium pratense).
J Agric Food Chem. 2005 Aug 10;53(16):6246-53. Overk CR, Yao P,
Department of Medicinal Chemistry and Pharmacognosy, UIC/NIH Center for
Botanical Dietary Supplements Research, College of Pharmacy, University of
Illinois, Chicago, Illinois
Because the prevailing form of hormone replacement therapy is associated with
the development of cancer in breast and endometrial tissues, alternatives are
needed for the management of menopausal symptoms. Formulations of Trifolium
pratense L. (red clover) are being used to alleviate menopause-associated hot
flashes but have shown mixed results in clinical trials. The strobiles of
Humulus lupulusL. (hops) have been reported to contain the prenylflavanone,
8-prenylnaringenin (8-PN), as the most estrogenic constituent. Extracts of hops
and red clover and their individual constituents including 8-PN,
6-prenylnaringenin (6-PN), isoxanthohumol (IX), and xanthohumol (XN) from hops
and daidzein, formononetin, biochanin A, and genistein from red clover were
compared using a variety of in vitro estrogenic assays. On the basis of these
data, hops and red clover could be attractive for the development as herbal
dietary supplements to alleviate menopause-associated symptoms.
In vitro and ex vivo cyclooxygenase inhibition by a
hops extract.
Lemay M, et al. Access Business Group LLC,
California, USA.
Asia Pac J Clin Nutr. 2004;13(Suppl):S110.
While there has been much research on botanical
materials as potential pain-relieving Cox inhibitors, it has not yet been
demonstrated that oral consumption of botanical agents can inhibit
Cox-2
activity in humans. In particular it would be of interest to determine whether
any botanical anti-inflammatory has Cox-1-sparing activity, in order to reduce
the risk of gastrointestinal side effects. This two-stage study was designed to
first screen a variety of botanicals in vitro, and then to select one or more
promising agents to test in human volunteers. Method: Seventeen botanical
agents, putative anti-inflammatories or pain-relievers all, were evaluated in
vitro for Cox-1 and -2 inhibitory potency and selectivity using a caco-2 cell
line with ibuprofen as an active control. A promising compound, a hops extract
high in alpha acids, showed a Cox-2/Cox-1 IC50 selectivity ratio of 0.06,
compared to 4.2 for ibuprofen. Two different formulations of a standardized hops
extract (resin and powder) were compared with ibuprofen in a double-blind,
randomized, ex vivo study. Subjects consumed hops powder extract, hops resin
extract, or ibuprofen, and provided blood samples before and at intervals for 9
h following the first dose. Plasma was extracted and analyzed in a validated
Cox-1 and -2 inhibition assay. Results: There were no differences between active
treatments or ibuprofen control in Cox-2 inhibitory action, as indicated by
9-hour Cox-2 Area over the Inhibition Curve (AOC); however, hops powder or hops
resin extract produced a 9-hour Cox-1 / Cox-2 AOC ratio of about 0.4 (i.e., some
degree of Cox-1 sparing), compared to 1.5 for ibuprofen (i.e. no Cox-1 sparing).
Conclusion: Hops exhibited Cox-2 inhibition over 9 hours equivalent to ibuprofen
400 mg but had significant Cox-1 sparing activity relative to ibuprofen. Hops
extracts may represent a safe alternative to ibuprofen for non-prescription
anti-inflammation.
The Fixed Combination of Valerian and Hops (Ze91019) acts via a
Central Adenosine Mechanism.
Institut fur Ganzheitliche Medizin und Wissenschaft, Huttenberg, Germany.
Planta Med. 2004 Jul;70(7):594-7.
The aim of the study was to demonstrate competition between caffeine and a
fixed valerian/ hops extract combination (Ze91019) by the central adenosine
mechanism. EEG was used to describe the action of caffeine on the central
nervous system after oral administration (200 mg) in healthy volunteers. In
addition to caffeine, the volunteers (16 in each group) received either placebo
or verum (2 and 6 tablets containing the valerian/ hops extract). The EEG
responses were recorded every 30 min thereafter. The valerian/ hops medication was
capable of reducing (2 tablets) or inhibiting (6 tablets) the arousal induced by
caffeine. This pharmacodynamic action was observed 60 minutes after oral
administration, indicating not only competition between the antagonist caffeine
and the partial agonist, i. e., the valerian/ hops extract but also
bio-availability of the compound(s) responsible for the agonistic action. In
conclusion, the valerian/ hops extract acts via a central adenosine mechanism
which is possibly the reason for its sleep-inducing and -maintaining activity.
Isohumulones, bitter acids derived from hops, activate both peroxisome
proliferator-activated receptor (PPAR) alpha and gamma and reduce insulin
resistance.
Yajima H,. Kirin Brewery Co., Ltd, Yokohama, Yokohama
236-0004.
J Biol Chem. 2004 Jun 3
The peroxisome proliferator-activated receptors (PPARs) are dietary lipid
sensors that regulate fatty acid and carbohydrate metabolism. The hypolipidemic
effects of fibrate drugs and the therapeutic benefits of the thiazolidinedione
drugs are due to their activation of PPARs alpha and gamma, respectively. In
this study, isohumulones, the bitter compounds derived from hops that are
present in beer, were found to activate PPARs alpha and gamma in transient co-transfection
studies. Among the three major isohumulone homologs, isohumulone and
isocohumulone were found to activate PPARs alpha and gamma. Diabetic KK-A(y)
mice that were treated with isohumulones (isohumulone and isocohumulone) showed
reduced plasma glucose, triglyceride, and free fatty acid levels (65.3, 62.6,
and 73.1%, respectively for isohumulone); similar reductions were found
following treatment with the thiazolidinedione drug, pioglitazone. Isohumulone
treatment did not result in significant body weight gain, though pioglitazone
treatment did increase body weight (10.6% increase vs. control group). C57BL/6N
mice fed a high fat diet that were treated with isohumulones showed improved
glucose tolerance and reduced insulin resistance. Furthermore, these animals
showed increased liver fatty acid oxidation and a decrease in size, and increase
in apoptosis, of their hypertrophic adipocytes. A double-blind,
placebo-controlled pilot study for studying the effect of isohumulones on
diabetes suggested that isohumulones significantly decreased blood glucose and
hemoglobin A1c levels after eight weeks (by 10.1% and 6.4%, respectively, vs.
week zero). These results suggest that isohumulones can improve insulin
sensitivity in high fat diet-fed mice with insulin resistance and in patients
with type 2 diabetes.
Comparative study for assessing quality of life of
patients with exogenous sleep disorders (temporary sleep onset and sleep
interruption disorders) treated with a hops-valarian preparation and a
benzodiazepine drug]
Schmitz M, Jackel M. Institut fur
Psychosomatik, Wien.
Wien Med Wochenschr. 1998;148(13):291-8.
This randomized, double-blind, controlled clinical trial in parallel group
design demonstrated equivalent efficacy and tolerability of a hop-valerian
preparation compared with a benzodiazepine preparation in patients suffering
from sleep disorders according to DSM-IV criteria. Sleep quality, fitness and
quality of life were determined by psychometric tests, psychopathologic scales
and sleep-questionnaires at the beginning of the therapy, end of therapy
(duration 2 weeks) and then 1 week after cessation of therapy. Patients' state
of health (4-point scale) and medication tolerability (occurrence of adverse
events) were documented. Using the following as parameters "Alphabetischer
Durchstreichtest, Feinmotoriktest, Befindlichkeitsskala, Beschwerdeliste,
Schlaffragebogen A and B" the differences between beginning and the end of the
therapy were analyzed by simultaneous testing of the equality or superiority of
the test preparation. The equivalence of both therapies according to sleep
quality, fitness and quality of life was proven by a Mann-Whitney-Statistic of
0.50 with a lower boundary of the 95% confidence interval of 0.46. The patients'
state of health improved during therapy while showing a deterioration after
cessation with both preparations. Withdrawal symptoms, however, were documented
with benzodiazepine. Only one adverse drug reaction was reported during this
study, namely stomach complaints from both the test and reference medication.
This study shows that the investigated hop-valerian preparation in the
appropriate dose is a sensible alternative to benzodiazepine for the treatment
of nonchronic and non-psychiatric sleep disorders.
Hops Flower Extract 0.30% Flavonoids
acetyl-l-carnitine
alpha lipoic acid
antioxidant
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Avena Sativa
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Creatine
Damiana
DHEA is a hormone
Erectile dysfunction
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Ginseng
Horny Goat Weed
Impotence
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Maca
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Resveratrol found in wine
Rhodiola
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Sexual
Enhancement
plants
Stinging nettle
Tribulus
Hops questions
Q. Is it okay for a man to use hops to help with sleep, seeing that hops
apparently has oestrogen-like properties?
A. We don't see any problems using hops by men, after
all men drink beer made from hops. Besides, many plants have compounds that have
estrogenic properties.
Q. Does
Theanine help with
anxiety? Can it be taken with hops herb?
A. L Theanine may be a mild anti-anxiety agent, but we
need more human studies to determine if this is true. I don't see any reason why
it can't be taken with hops herb.
Hops Plant
herb hops and stress hops for anxiety