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(Brent) #1

In the case of Rikkunshito, a low-dose preparation was used as a placebo
control because of difficulty in developing control granules.
In a separate double-blind, controlled study for re-evaluation, Chotosan
(Siao-Tang-San)was also shown to have a beneficial clinical effect in the
treatment of vascular dementia.^26
Although kampo medicines have a long clinical experience, they also need
an objective clinical evaluation as evidence-based medicine (EBM). However,
kampo medicines have traditionally been used according to the disturbed
pathophysiological conditions of the patient (so-calledshoclinically), so clin-
ical study of kampo medicines needs to consider the concept ofsho.^27 In clin-
ical trials, objects should be chosen depending on the status ofsho, e.g. the
trial can be limited to patients showing a hypofunctioning condition. The
design of the trial is very important for clinical study of kampo medicine.
Kampo medicines have to consider two judgements in EBM: one is the
most reliable scientific proof and the other is the specific clinical situation


Japanese kampo medicine | 245

Shakuyakukanzoto
Maintenance of contractility against muscle clamping model
Shimotsuto
Anti-stress effect
Reversal effect of scopolamine-induced impairment in the radical maze performance
Delay of the development of the infarction and rarefaction following chronic ischaemia of the brain
Anti-metastatic activity
Saibokuto
Suppression of experimental allergic reactions
Suppression and antagonistic actions on release and production of chemical mediators
Suppression of decrease of b-receptor
Suppression of decrease of glucocorticoid receptor
Suppression of induction of IgE Fcereceptor II in lymphocytes from asthma patient
Improvement of tracheal mucociliary tract
Ninjinyoeito
Immunomodulating activity (suppression of decrease of NK activity in spleen cells)
Improvement of passive avoidance behaviour in hyoscine administered mouse
Saireito
Diuretic activity
Anti-inflammatory activity (increase of blood ACTH level, increase of corticosterone secretion from
adrenal gland)

Table 8.5Continued

5HT, 5-hydroxytryptamine (serotonin); ACTH, adrenocorticotrophic hormone; ChAT, choline
acetyltransferase; FSH, follicle-stimulating hormone; hCG, human chorionic gonadotrophin; Ig,
immunoglobulin; IL, interleukin; LH, luteinising hormone; NGF, nerve growth factor; NKT, natural killer/T
cells; PAF, platelet-activating factor; PG, prostaglandin; SHR-SP, stroke-prone spontaneously hypertensive
rats; Th, T-helper cell.
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