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Anti-aging Research > Chrysin.
Chrysin
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News & Research:
- Chrysin: Is It An Effective
Aromatase Inhibitor? - vrp.com - "Unfortunately,
there does not appear to be any effective natural inhibitor of aromatase"
-
Replenish Testosterone Naturally - Life Extension Magazine, 1/00 -
"chrysin and 10 other flavonoids were compared to an
aromatase-inhibiting drug (aminoglutethimide). The study tested the
aromatase-inhibiting effects of these natural flavonoids (such as genistein,
rutin, tea catechins, etc.) in human fat cell cultures. Chrysin was the most
potent aromatase-inhibitor, and was shown to be similar in potency and
effectiveness to the aromatase-inhibiting drug ... Chrysin, for example, is
a potent antioxidant that possesses vitamin-like effects in the body ...
Chrysin was shown to produce anti-anxiety effects comparable with diazepam,
but without sedation and muscle relaxation. In other words, chrysin produced
a relaxing effect in the brain, but with no impairment of motor activity ...
chrysin can reduce anxiety without inducing the common side-effects
associated with benzodiazepine drugs ... chrysin displayed potent
anti-anxiety effects in rats, but did not interfere with cognitive
performance ... chrysin selectively inhibits anxiety in the brain but,
unlike diazepam, does not induce the cognitive impairment ... Chrysin may
therefore offer libido-enhancing effects in the aging male by: Increasing
free testosterone, - Decreasing excess estrogen, - Producing a safe
anti-anxiety effect"
-
Male
Hormone Modulation Therapy - Life Extension Magazine, 11/99
-
Monthly Updates - Hair Loss Research, 10/01 -
"While finasteride (Propecia/Proscar) decreases
serum DHT, it also is thought to increase estrogen which suggests that men
over 35 may want to consider using it in conjunction with a systemic
aromatase inhibitor such as Chrysin/Piperine
(Super Miraforte),
Arimidex, or stinging nettle extract, to
maximize its hair growth effects and minimize potential side effects (that
are listed in the PDR) such as
Gynocaemastia (breast enlargement in
males), sexual side effects, and an increase in fat deposition. These
compounds have been reliably shown to increase testosterone and reduce
excess estrogen, resulting in a youthful hormone profile that optimizes
immune function and to some degree, body composition"
Abstracts:
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Lycopene and Chrysin through
Mitigation of Neuroinflammation and Oxidative Stress Exerted Antidepressant
Effects in Clonidine-Induced Depression-like Behavior in Rats - J Diet Suppl
2021 Oct 11;1-20 - "Depression is a severely
debilitating psychiatric disorder that influences more than 15% of the
population worldwide. It has been demonstrated that it is associated with a high
risk of developing other diseases such as cardiovascular diseases, diabetes,
stroke, epilepsy, and cancer ... The rats in group 1 served as a control. Group
2 received lycopene only. Group 3 was provided chrysin only. Group 4 was
administered clonidine and served as the model. Group 5 was offered lycopene and
clonidine. Group 6 was administered chrysin and clonidine. Group 7 was given FLX
and clonidine and represented the standard ... The current research demonstrates
that lycopene and chrysin have an auspicious antidepressant effect against
clonidine that provoked behavioral hopelessness in rats. Manipulating oxidative
stress, inflammation, and apoptosis may partially represent the corrective
mechanism for the neuroprotective actions against the depressive effect of
clonidine" - See lycopene at Amazon.com and
iHerb and chrysin at Amazon.com.
-
Chrysin Protects against
Memory and Hippocampal Neurogenesis Depletion in D-Galactose-Induced Aging in
Rats - Nutrients. 2020 Apr 16 - "The interruption of
hippocampal neurogenesis due to aging impairs memory. The accumulation of D-galactose
(D-gal), a monosaccharide, induces brain aging by causing oxidative stress
and inflammation, resulting in neuronal cell damage and memory loss.
Chrysin, an extracted flavonoid, has neuroprotective effects on memory ...
Male Sprague-Dawley rats received either D-gal (50 mg/kg) by i.p. injection,
chrysin (10 or 30 mg/kg) by oral gavage, or D-gal (50 mg/kg) and chrysin (10
or 30 mg/kg) for 8 weeks. Memory was evaluated using novel object location
(NOL) and novel object recognition (NOR) tests. Hippocampal neurogenesis was
evaluated using Ki-67, 5-bromo-2'-deoxyuridine (BrdU), and doublecortin
(DCX) immunofluorescence staining to determine cell proliferation, cell
survival, and number of immature neurons, respectively. We found that D-gal
administration resulted in memory impairment as measured by NOL and NOR
tests and in depletions in cell proliferation, cell survival, and immature
neurons. However, co-treatment with chrysin (10 or 30 mg/kg) attenuated
these impairments. These results suggest that chrysin could potentially
minimize memory and hippocampal neurogenesis depletions brought on by aging"
- See chrysin at Amazon.com and
chrysin at
iHerb.com.
-
Chrysin
Suppresses IL-6-Induced Angiogenesis via Down-regulation of JAK1/STAT3 and
VEGF: An in Vitro and in Ovo Approach - J Agric Food Chem. 2010 May 5 -
"Chrysin may provide new therapeutic potential for
IL-6-induced pathological angiogenesis"
-
Chrysin sensitizes tumor necrosis factor-alpha-induced apoptosis in human
tumor cells via suppression of nuclear factor-kappaB - Cancer Lett. 2010
Feb 2 - "In the present study, we found that,
pretreatment with chrysin greatly sensitized various human cancer cells to
tumor necrosis factor-alpha (TNFalpha)-induced apoptosis"
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Inhibition of aromatase activity by flavonoids - Arch Pharm Res. 1999
Jun;22(3):309-12
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Flavonoid inhibition of aromatase enzyme activity in human preadipocytes
- J Steroid Biochem Mol Biol. 1993 Sep;46(3):381-8 -
"Chrysin, the most potent of the naturally-occurring
flavonoids, was similar in potency and effectiveness to AG, a pharmaceutical
aromatase inhibitor used clinically in cases of estrogen-dependent
carcinoma."
-
Inhibition of human estrogen synthetase (aromatase) by flavones -
Science. 1984 Sep 7;225(4666):1032-4 -
"7,8-Benzoflavone and chrysin were potent
competitive inhibitors and induced spectral changes in the aromatase
cytochrome P-450"
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