Icariin
extract
and erectile enhancement, epimedium herb source, benefit for impotence treatment
Icariin, a flavonol glycoside, is an interesting substance found in
certain herbs, particularly
horny goat weed.
Erection enhancer
Icariin appears to have some properties similar to Viagra. It is a cGMP-specific PDE5 inhibitor that may
have potential in treating erectile dysfunction. Additional herbs helpful for
sexual improvement include
tongkat ali and mucuna pruriens.
Epimidium Sagittatum with icariin
extract pills


Epimedium sagittatum 200 mg has
epimedium extract (standardized to
20% flavonoids as icariin).
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Icariin and
phosphodiesterase activity for erectile dysfunction
Effects of icariin on phosphodiesterase-5 activity in vitro and cyclic
guanosine monophosphate level in cavernous smooth muscle cells.
Urology. 2006.
To investigate the effect of icariin on the cyclic guanosine
monophosphate (cGMP)-hydrolytic activity of phosphodiesterase-5 (PDE5) isoforms
and the cGMP levels in cavernous smooth muscle cells treated with sodium
nitroprusside. PDE5 isoforms (PDE5A1, A2, and A3) were isolated from sf9
insect cells infected with baculoviruses carrying PDE5 isoform cDNA. Icariin was
isolated from Epimedii herba. Icariin was inhibitory to all three PDE5 isoforms
with similar IC50 values, which were approximately three times greater than
those for zaprinast. Icariin was able to enhance cGMP levels in sodium
nitroprusside -treated cavernous smooth muscle cells.
Additional benefits
In laboratory studies, icariin appears to have anti- cancer
and anti-inflammatory abilities. Icariin
also helps protect the liver from toxicity and DNA from damage.
Antioxidant
Protective effect of icariin on DNA against
radical-induced oxidative damage.
J Pharm Pharmacol. 2007.
Icariin
is a concentration-dependent chemopreventor in protecting DNA against
radical-induced damage.
Brain cell protection
Icariin attenuates lipopolysaccharide-induced microglial activation and
resultant death of neurons by inhibiting TAK1/IKK/NF-kappaB and JNK/p38 MAPK
pathways.
Int Immunopharmacol. 2010.
Our findings provide
mechanistic insights into the suppressive effect of icariin on LPS-induced
neuroinflammatory response in microglia, and emphasize the neuroprotective
effect and therapeutic potential of icariin in neuroinflammatory diseases.
Icariin inhibits the increased inward calcium
currents induced by amyloid-beta(25-35) peptide in CA1 pyramidal neurons of
neonatal rat hippocampal slice.
Am J Chin Med. 2010. Department of
Integrated Chinese and Western Medicine, First Hospital, Peking University,
Beijing, China.
Overload of intracellular calcium caused by amyloid-beta peptide has
been implicated in the pathogenesis of neuronal damage in Alzheimer's disease.
Icariin nearly complete suppressed the abnormal inward calcium currents induced
by Abeta(25-35) in a dose-dependant manner. Our findings suggest that the
potential neuroprotective effect of icariin on Abeta(25-35)-induced
neurotoxicity via the balance intracelluar calcium homeostasis.
Osteoporosis and bone health
Effect of icariin on the mRNA expressions of Cbfalpha1, BMP2, BMP4 in rat
osteoblasts
Beijing Da Xue Xue Bao. 2009; Center of Orthognathic Surgery,
Peking University School and Hospital of Stomatology, Beijing, China
Icariin promotes the differentiation ability of rat osteoblasts
through upregulating the Cbfalpha1, BMP2, BMP4 mRNA expressions.
Metabolism and excretion
J Agric Food Chem. 2010. Analysis of biliary excretion of icariin in rats.
Institute of Traditional Medicine, School of Medicine, National Yang-Ming
University, Taipei, Taiwan.
Icariin is a bioactive herbal ingredient isolated from Epimedii Herba. This study
evaluates its distribution n rats by microdialysis sampling and high-performance
liquid chromatography with ultraviolet detection (HPLC-UV). Microdialysis probes
were simultaneously placed in the jugular vein, brain striatum, and bile duct of
each anesthetized rat for sampling after the administration of icariin via the
femoral vein. This study is the first report of the biliary excretion of icarin
in rats. This work demonstrates that biliary excretion is the major elimination
pathway for icariin disposition and that transporters, such as P-gp, might be
related to it's biliary excretion.