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| SST (Sho-saiko-to) |
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The Herbal Formula:
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Minor
Bupleurum Formula Extract
(Sho-saiko-to; Xiao Chai Hu Tang) |
| Description: |
| The daily dose of 7.5g (6 capsules) contains 4.20g of Minor Bupleurum Formula extract: |
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Bupleurum Root (Chai hu)
Pinellia Tuber (Ban xia)
Scutellaria Root (Huang qin)
Ginseng (Ren shen)
Jujube (Da zao)
Licorice (Gan cao
Ginger (Sheng jiang) |
7.0g
5.0g
3.0g
3.0g
3.0g
2.0g
1.0g |
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Standardization Specification:
This product is standardized to contain 24.7-46.0 mg/day of Glycyrrhizin, 110.6-205.6 mg/day of Baicalin, and 6.5-19.7 mg/day of Saikosaponin.
Duration of Use:
The Clinical Studies at Memorial Sloan-Kettering are a one year duration of constant use. Some of the studies in Japan followed patients for as long as seven years. There is apparently no problem with long term consistent usage.
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A mixture
of seven herbs: Bupleurum Root (Chai hu), Pinellia Tuber (Ban
xia),
Scutellaria Root (Huang qin), Ginseng (Ren shen), Jujube (Da
zao), Licorice (Gan cao), and Ginger (Sheng jiang). |
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A number of pharmacologically active components have been isolated including Baicalin,
Baicalein,
Glycyrrhizin,
Saikosaponins,
Ginsenosides,
Wogonin,
and Gingerols.
Given the complexity of Sho-saiko-to, it is unlikely that all active components have been identified. |
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Dosage and
Administration: |
| For adults: 7.5g per day orally divided into 2 doses before or between meals. This translates to 3 capsules, 2 times per day. The dosage may be adjusted based on age, body weight and symptoms. |
Scientific Research Data (using Sho-saiko-to in granular form): |
| The
Animal Data: |
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In vitro
research with Sho-saiko-to and its individual components
indicates that this compound may prevent hepatic fibrosis and
effectively treat Hepatitis C. |
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Glycyrrhizin,
a triterpenoid saponin extract from licorice root, displays
in vitro and in vivo ability to reduce serum aminotransferases
and improve hepatic fibrosis. |
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Baicalein, a
major flavonoid in Scutellaria, has antiproliferative
and anti fibrogenic effects when tested in hepatic stellate
cells from rats in vitro. |
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Ginseng has been
shown to inhibit the development of HCC in mice induced
by diethylnitrosamine, aflatoxin B1 and a N-nitroso diethylamine
and phenobarbital combination. |
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In rats with dimethylnitrosamine-induced
liver injury, Sho-saiko-to displayed inhibition of collagen formation,
increased retinoid level, inhibited activation of Ito cells,
and prevented liver fibrosis. |
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Sho-saiko-to was shown
to prevent liver injury and promote liver regeneration in animal
models. |
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| The
Human Data: |
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In a randomized
trial conducted in Japan in the 1980s, 222 patients with chronic
active Hepatitis B diagnosed by biopsy received either Sho-saiko-to or placebo for 12 weeks. There were statistically significant
differences between groups in Aspartate Transaminase (AST) and
Alanine Transaminase (ALT). There was an increase in anti-Hbe
antibody during treatment in the Sho-saiko-to but not in the placebo
group. |
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An uncontrolled
trial of Sho-saiko-to for Hepatitis B in children reported that
seven of fourteen became HbeAg negative at the end of one year. |
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In a controlled
study, 80 patients with interferon-resistant Hepatitis C were
treated with Sho-saiko-to plus unspecified 'conventional medicine'
or conventional medicine alone. The patients were followed for
7 years. During this time, five patients on Sho-saiko-to experienced
normalization of liver enzymes in full and one seroconverted.
Enzymes normalized in only one patient in controls and none
seroconverted. Conversely, five controls progressed to hepatocellular
carcinoma versus one on Sho-saiko-to therapy. No adverse effects
were reported. |
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Long-term
effect of Sho-saiko-to on the level of markers for hepatic fibrinogenesis
in chronic Hepatitis C: |
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93
Chronic Hepatitis C patients were prescribed Sho-saiko-to three times daily for 36 months. |
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Long-term administration
of Sho-saiko-to has been shown to have an anti-hepatic fibrinogenesis
effect for chronic Hepatitis C patients. |
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There is
evidence that Sho-saiko-to might benefit hepatitis patients by
preventing progression to hepatocellular carcinoma (HCC). A
large prospective study was conducted in Japan in the late 1980s
and published in Cancer in 1995. |
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260
patients with cirrhosis were randomized to treatment with
Sho-saiko-to or control. |
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HCC was the primary
endpoint and was confirmed by angiography, CT and biopsy. |
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Patients were
followed for five years of bimonthly a-fetoprotein measurements
and quarterly ultrasonography. |
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Sho-saiko-to led to a
one-third reduction in the incidence of HCC (23% vs. 34%) and
40% reduction in deaths (24% vs. 40%). |
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TCM (Traditional
Chinese Medicine) Formulation Strategy This Remedy is Based Upon: |
| Chai hu, the chief
herb, combined with the deputy herb huang qin, vent the pathogenic
influence and release the half exterior aspects in the lesser yang
stage. The assistant herb, ban xia, warms and transforms phlegm and
turbidity in the middle burner, and the other assistant herb, sheng
jiang harmonize the middle burner to stop nausea and vomiting. Ren
shen, zhi gan cao and da zao support middle burner qi and thereby
prevent the pathogenic influence from penetrating into the interior.
Zhi gan cao is also an envoy, and can harmonize whole drug actions. Based
on the combination of these herbs, this formula can regulate lesser
yang-stage disorders. |
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| Clinical
Trials: |
| Phase
II Study of Sho-saiko-to in Patients with Chronic Hepatitis C Who
Cannot Use Interferon |
| Sho-saiko-to
Following Removal of Liver Cancer By Embolization in Treating Patients
With Liver Cancer That Cannot Be Surgically Removed |
For More Information, visit:
Memorial Sloan-Kettering Cancer Center |
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