Pain X (therapeutic) | Biogenesis Nutraceuticals
90 veggie capsules $31.98
What is Pain-X Anti-inflammatory? DL Phenylalanine (DLPA):
has putative antidepressant and analgesic (pain relieving) properties.
Pain-X
Anti-inflammatory: Pain reduction may occur by limiting
enkephalin degradation by the enzyme carboxypeptidase A. The LPA
portion acts as a precursor to the synthesis of norepinephrine and
dopamine. This effect may explain DLPAs putative antidepressant
activities. DLPA is contraindicated in those with phenylketonuria,
and those taking nonselective MAO inhibitors.
Pain-X Anti-inflammatory:
- Reduction of pain and inflammation
- recommended use for acute and chronic conditions
Boswellia: has been used in traditional Indian
medicine for chronic rheumatic inflammation. Boswellic acids have
been shown to inhibit 5-lipoxygenase the enzyme in leukotriene biosynthesis.
It is this property along with its ability to inhibit both the classical
and alternative complement pathways that accounts for its anti-inflammatory
properties.
Curcumin: the yellow pigment from the plant Curcuma
longa, has been used traditionally to treat sprains and inflammation.
Studies show that curcumin inhibits leukotriene synthesis, platelet
aggregation, neutrophil inflammatory response, blocks activation
of NF Kappa B and promotes fibrinolysis. Curcumin may potentiate
endogenous corticosteroids, thus having indirect anti-inflammatory
actions as well. Curcumin was as effective as cortisone or phenylbutazone
in models of acute inflammation, but only half as effective in chronic
models. However, while phenylbutazone and cortisone are associated
with significant toxicity, curcumin displayed virtually no toxicity.
Bromelain: was introduced as a medicinal agent
in 1957, and since that time over 400 scientific papers on its therapeutic
applications have appeared. Bromelain has been reported in these
studies to exert a wide variety of beneficial effects, including
reducing inflammation in cases of joint disease, sports injury or
trauma, and preventing swelling after trauma or surgery. Bromelain
selectively stimulates the production of the anti-inflammatory Prostaglandin
E1 and inhibits the production of the pro-inflammatory Prostaglandin
E2.
Note: Bromelain may enhance the anticoagulant activity
of such drugs as warfarin and aspirin.
White Willow Bark: is traditionally used to treat
pain. The efficacy of this botanical is due mainly to the proportion
of salicin present. The salicin which is a precursor to salicylic
acid works as an antipyretic, antiphlogistic and as an analgesic.
Guggal: has been used traditionally for inflammation
of the mouth and pharynx. Currently guggal is recommended for chronic
inflammatory conditions.
Bioflavonoids: have been shown to possess antioxidant,
anti-inflammatory, anti-allergic, and vasoprotective actions. Hesperidin
appears to inhibit phospholipase A2, lipoxygenase and cyclo-oxygenase
inflammatory mediators as well as inhibit histamine release.
Ginger: inhibits platelet thromboxane formation,
lipoxygenase, Arachidonic acid metabolism, leukotriene and inflammatory
prostaglandin production. Ginger has anti-inflammatory actions.
In one small study, consisting of 10 patients, complaining of chronic
muscular pain and discomfort, ginger relieved the pain and swelling
in 100% of the patients. These patients were evaluated for periods
ranging from 3 months to 2.5 years.
Rosemary: has a traditionally been recommended
for muscular rheumatism. Rosemary has antioxidant actions.
Papain, Trypsin and Alpha Chymotrypsin: are proteolytic
enzymes. Administration of proteolytic enzymes may speed healing
of injuries. Proteolytic enzymes have allowed athletes to return
to performance sooner than control groups. Chymotrypsin, and trypsin
have been shown to reduce edema and inflammation.
How Do I Use Pain-X? Suggested Dose: As a dietary
supplement, take 1-2 capsules without food three times per day or
as directed by a health care professional.
Pain-X Supplement Facts:
References:
Ehrenpreis S. Pharmacology of enkephalinase inhibitors: animal
and human studies. Acupunct Electrother Res. 1985; 10:203-208.
Walsh ND, Ramamurthy S. Schoenfeld L, Hoffman J. Analgesic effectiveness
of D-phenylalanine in chronic pain patients. Arch Phys Med Rehabil.
1986; 67:436-439.
Webach, MR, Murray MT. Botanical Influences on Illness: A sourcebook
of clinical research. Third Line Press, Tarzana, CA, 2000.
Rall B et al., Boswellic acids and protease activity (s. auch folgende
Abstracts). In: PM 61 (Abstracts of 43rd Ann Congr): 105. 1995.
Singh GB, Singh S, Bani S. Anti-inflammatory actions of boswellic
acids. Phytomedicine 3(1):81-5, 1996.
Srimal R, Dhawan B. Pharmacology of diferuloyl methane (curcumin),
a non-steroidal anti-inflammatory agent. J Pharm Pharmac 25: 447-52,
1973.
Taussig S, Batkin S. Bromelain, the enzyme complex of pineapple
(Ananas comosus) and its clinical application. An update. J Ethnopharmacol
22:191-203, 1988.
Taussig SJ. The mechanism of the physiological action of bromelain.
Med Hypothesis 6:99-104, 1980.
Vellini M et al. Possible involvement of eicosanoids in the pharmacological
action of bromelain.
Arzneimittelforschung 36:110-12, 1986.
PDR for Herbal Medicines, Medical Economics Company, Montvale,
New Jersey. 1998.
Emin JA, Oliveira AB, Lapa AJ. Pharmacological evaluation of the
anti-inflammatory activity of a citrus bioflavonoid, hesperidin,
and the isoflavonoids duartin and claussequinone in rats and mice.
J Pharm Pharmacol. 46:118-122, 1994.
Srivastava KC and Mustafa T. Ginger (Zingiber officinale) in rheumatism
and musculoskeletal disorders. Med Hypothesis 39:342-8, 1992.
Cichoke AJ, Marty L. The use of proteolytic enzymes with soft tissue
athletic injuries. Am Chiropractor October 1981, p. 32.
Taraye JP, Lauressergues H. Advantages of a combination of proteolytic
enzymes, flavonoids and ascorbic acid in comparison with non-steroidal
inflammatory agents. Arzneim Forsch 27(1):1144-49, 1977.
This information is not intended as medical
advice. This information is not intended to provide you a diagnosis
or a plan of care. If you are not feeling well, please consult your
health care provider. If you are presently being treated by another
provider, do not disregard that provider's treatment plan because
of anything that you read on this website. If you have any questions,
please call or email us. Your well-being is our primary concern.
*These statements have not been evaluated by
the Food and Drug Administration. This product is not intended to
diagnose, treat, cure or prevent any disease.
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