298 lines
14 KiB
Plaintext
298 lines
14 KiB
Plaintext
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Astragalus Membranaceous & White Blood Cell Function
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Patricia Wolf B.Sc. N.D.
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Introduction
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Traditional Chinese medicine as practised today had its
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theoretical and philosophical tenets first outlined in the Yellow
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Emperor's Inner Classic, written between 200 and 100 BC. The
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Inner Classic promotes the use of herbs, acupuncture, dietary
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management and exercise as therapeutic modalities (Bensky,
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Gamble).
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Centuries of careful observation and empirical study have
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resulted in an extremely detailed and refined system of herbal
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use according to traditional Chinese medical theory (TCM).
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However, very little is known about the mechanism of action or
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the physiological effects of most Chinese herbs in terms of
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modern Western medical thought. Recently, research has been
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conducted, mostly in China, in an attempt to elucidate these
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areas.
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Radix Astragali, the root of Astragalus membranaceous (Huang
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Ch'i), is a popular tonic herb first described in the Divine
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Husbandman's Classic of the Materia Medica, a text reconstructed
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and edited from several earlier works by Tao Hong-Jing in the
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6th. Century A.D.(Bensky et al). According to TCM, Radix
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Astragali affects the Spleen, Lung and Triple Warmer meridians.
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It specifically tonifies the exterior, or protective energy (Wei
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Chi), which is understood to be the body's first defence against
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the external disease factors (ie., Wind, Cold, Damp, Heat,
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Dryness). Huang Ch'i also tonifies Chi, especially the Yang Chi
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of the Spleen and Stomach. It tonifies Blood and regulated fluid
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metabolism (Bensky et al; Teeguarden).
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Modern research has revealed several effects of Radix Astragali.
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Of primary interest to the author is the herbs's reputed
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stimulatory effect on the immune system. Teeguarden reports on
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Chinese studies which have shown Astragalus to have in vitro
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anti-bacterial effects, as well as an inhibitory effect on T-
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suppressor cells. He also cites clinical trials on cancer
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patients which suggest that Astragalus enhances bone marrow
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activity and adrenal cortical function which had been depleted by
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chemotherapy and/or radiation treatment. (The original papers
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were not available for perusal.)
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One study found that Radix Astragali significantly enhanced
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interferon production in mice, in human cell cultures and in
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vitro leucocyte samples (Hou, Ma, Wu, Li, Li). These workers also
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describe a clinical trial showing that a combination of human
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interferon and Astragalus was more effective in preventing common
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cold symptoms than either interferon alone or a flu vaccine. In
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one of the few Western studies conducted, Astragalus was found to
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restore T-cell function in cancer patients with an impaired
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immune response, and to augment T-cell function in normal donors
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(Sun, Hersh, Talpaz, Lee, Wong, Loo, Mavligit).
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This paper will report on the effect of Radix Astragali on white
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blood cell (WBC) status in human volunteers as reflected by WBC
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differential count and by "Liv Cell" analysis.
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Abstract
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The effect of a decoction of the Chinese tonic herb Astragalus
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membranaceous on certain aspects of white blood cell (WBC) status
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was studied in seven healthy volunteers. After a one week course
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of treatment with Astragalus decoction at a dosage equivalent to
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1.5g of dried root t.i.d. per os, the relative number of
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leucocytes was significantly increased (p <20> 0.01). Furthermore,
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this effect was sustained (p <20> 0.05) one week after treatment had
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been discontinued. A WBC differential count showed significant
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changes in the proportions of individual categories of leucocytes
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(p <20> 0.05), such that high or low percentages of leucocytes were
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brought into normal range, with the exception of basophils, which
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remained high. This effect was also sustained one week after
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treatment had been discontinued (p <20> 0.05). A `Liv Cell' analysis
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did not yield significant (p <20> 0.05), but this may have been a
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function of the criteria chosen to measure WBC status. This study
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suggests that Astragalus membranaceous may have a regulatory
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effect on WBC status and therefore may be a useful treatment in
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conditions of bo the deficient and excess (or disproportionate)
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WBC levels.
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Materials and Methods
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Herbal Preparation:
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454 grams of grade `A' quality dried Astragalus root was obtained
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from Nam Pek Hong, a reputable Chinese herb store in Toronto's
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Chinatown. The root was placed in 9.09 l. distilled water,
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brought to a boil, and then simmered to half the original volume
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of water, The extractive was poured off and saved. An additional
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6.82 l. distilled water was added to the herb, brought to the
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boil and similarly simmered to half the original volume. This
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extractive was added to the first and white vinegar was also
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added to 4.5% of the final solution as a preservative. The final
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decoction yielded unit doses of 42.6 ml., equivalent to 1.5 g. of
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dried root.
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The placebo solution was prepared by boiling potato with onion
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skins in distilled water to obtain the required colour, and
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adding white vinegar in 4.5% of the final solution.
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Subjects:
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Twelve healthy volunteers were recruited and randomly divided
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into two groups of eight and four subjects, treatment and placebo
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groups respectively. Subjects were asked to refrain from using
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any other treatment modalities or making any dietary or lifestyle
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changes during the test period.
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Experimental Design and Procedure:
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A double blind format was used. Blood samples were obtained by
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finger prick on days 1, 8, and 15. The herbal decoction or
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placebo was taken for 6 days, from day 2 to 8 inclusive. The
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dosage was 42.6 ml. three times a day. A WBC differential count
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and `Liv Cell' analysis (product information) were performed on
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the blood samples by a technician blind to the experimental
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conditions.
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For the `Liv Cell' analysis, 25 WBC's were examined for each
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subject. Five categories were used to indicate WBC status,
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namely, the number of WBC's showing:
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1. phagocytized material
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2. streaming of cytoplasm/chemotaxis
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3. irregular borders
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4. spilling of contents/degeneration
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5. no apparent activity
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Categories 1 and 2 were considered indicative of positive WBC
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function and given a score of +1 for each cell in either of these
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categories. Categories 3, 4 and 5 were chosen as negative
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parameters of WBC status and cells appearing in them were given a
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score of -1 each. Overlap between categories was allowed; thus a
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cell showing characteristics of more than one category would be
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entered under each. Therefore the maximum score possible for
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optimal WBC function would by 50 (ie. 25 in each of categories 1
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and 2, and 0 in categories 3, 4 and 5). The final score was used
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as an index of WBC status and comparisons were made between all
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possible pairs of scores.
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Statistical Analysis:
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The number of fields examined to yield a count of 100 WBC's was
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taken as an indication of the relative numbers of WBC's per
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sample. Statistical analysis of the changes in the number of
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fields between pretreatment with Astragalus and post treatment
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samples taken at one and two weeks respectively, was performed
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using a right-tailed Student's t-test for paired data at p <20> 0.05
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level of significance. Similarly, the same test was used to
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analyze the change in the proportion of individual types of
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leucocytes, except that a two tailed test was used. Student's t-
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test (right-tailed) was also used to analyze the difference
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between the WBC index score obtained from the `Liv Cell'
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analysis.
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Results
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All but one treatment subject showed a decrease in the number of
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fields needed to locate 100 WBC's in the differential count,
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indicative of a relative increase in the total number of WBC's
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after treatment with Astragalus. The one subject who showed a
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slight increase in the number of fields had the lowest number of
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fields initially (100 as compared to the mean of 410 fields). The
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mean difference in numbers of fields studied was 183.9 and the
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difference was significant at p <20> 0.01. Furthermore, the change
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was maintained in sample number 3 taken one week after
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discontinuing the Astragalus (p <20> 0.05).
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Each of the five types of leucocytes showed a significant change
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in their proportions of the total count immediately after
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treatment at p <20> 0.05 level of significance. The changes appeared
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to be regulatory, such that relatively low proportions were
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increased while high proportions were decreased.
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In most cases, except for the basophils, the differential count
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was brought more in line with the expected normal frequencies for
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adults (ie. neutrophils, 50 - 70%; lymphocytes, 20 - 40%;
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monocytes, 2 - 10%; eosinophils, 1 - 4%; basophils <20> 0.5%).
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The "immune index" scores obtained using `Liv Cell' analysis did
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not show an effect at the p <20> 0.05 level of significance.
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However, the mean difference (4.71) was only 0.40 units below the
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upper limit of acceptance for the null hypothesis (5.11).
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Furthermore, a significant negative change in the immune index
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score was shown by only one subject, and if this subject is
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omitted from the statistical analysis of results, the mean change
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in scores increases significantly at the p <20> 0.05 level.
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It was not possible to statistically compare the treatment group
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with the placebo group, as only one subject in the placebo group
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completed the study.
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Discussion
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Radix Astragali has long been used in traditional Chinese
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medicine as an important tonic herb. More recently, it has come
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under scrutiny regarding its physiological actions as understood
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in Western Medical theory. Among these is the herb's reputed
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positive effect on the immune system. This study has attempted to
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determine the effect of Astragalus decoction on certain
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parameters of WBC activity.
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Astragalus was seen to have a stimulatory effect on the relative
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numbers of leucocytes at the p <20> 0.01 level of significance. The
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relative proportions of individual categories of
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leucocytes were also significantly affected by treatment with
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Astragalus (p <20> 0.05), such that high proportions were lowered
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and low proportions were raised. This effect applied to both the
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variance between sample means and the variance within samples.
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Specifically, four subjects had above normal baseline proportions
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of monocytes &/or eosinophils, while three subjects had below
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normal proportions. In each case, treatment with Astragalus
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brought the proportions within normal ranges. Thus
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Astragalus appears to have a regulatory or amphoteric effect on
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individual classes of leucocytes in the WBC differential count.
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Furthermore, these effects seem to be sustained over time as the
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results obtained one week after discontinuing treatment indicate.
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This finding corroborates observations made by Hou et al.
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In addition to the WBC differential, a `Liv Cell' analysis was
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used in an attempt to support findings. The Liv Cell technique
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allows observation of living, unstained blood corpuscles and
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their activity. However, criteria for standard assessment is not
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well established for this method. An attempt was made to choose
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and weight parameters visible by Liv Cell analysis which would
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provide a measure of immune status. The parameters chosen yielded
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results that were just below the p <20> 0.05 level of significance
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and that lend support to the findings obtained using the WBC
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differential, namely, that Astragalus appears to have an
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enhancing effect on leucocyte function. The Liv Cell affords
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valuable and unique information about the dynamic state of the
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blood, but more work needs to be done in setting definite
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criteria for both quantitative and qualitative analysis.
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Although the sample size in this study was small, the results
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would seem to warrant further investigation into the area of
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enhancement of the immune system by Astragalus. Specifically, a
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larger sample size with a placebo control group would be in
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order. In addition to WBC differential count, a total WBC count
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should be performed. It would also be interesting to screen
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subjects to recruit those with both high and low baseline
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differentials for specific categories of leucocytes to test the
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hypothesized regulatory effect of Astragalus suggested by this
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study. Furthermore, a longer treatment time with follow-up
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samples taken over several months (see Hou et al) would provide
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more information about the long term effects.
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If Astragalus is consistently found to regulate leucocyte
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activity, it may be a valuable adjunct in the treatment of both
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immune deficient conditions and conditions of aberrant
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leucocytosis, such as leukaemia.
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References
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Bensky, D., Gamble, A. (compiled & translated by). Chinese Herbal
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Medicine Materia Medica. Eastland Press Inc., P.O. Box 12689,
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Seattle, Washington 9811; 1986. p.3
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Ibid. p.5, p.457
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Ibid. pp. 457 - 9
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Hou, Y., Ma, G., Wu, S., Li, Y., Li, H. "Effect of Radix
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Astragali seu Hedysari on the Interferon System". Chinese Medical
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Journal, 94(1): 35 - 40, 1981.
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Sun, Y., Hersh, E.M., Talpaz, M., Lee, S-L., Wong, W., Loo, T.L.,
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Mavligit, G.M. "Immune Restoration and/or Augmentation of Local
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Graft Versus Host Reaction by Traditional Chinese Medicinal
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Herbs". Cancer 52:70 - 73, 1983.
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Teeguarden, R. Chinese Tonic Herbs. Japan Publications Inc., New
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York 1984. pp. 98 - 101.
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This Article is taken from The Herbalist, newsletter of the
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Canadian Herbal Research Society. COPYRIGHT June 1988.
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Membership in the Society is $25.00 Canadian per year. You
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receive four copies of the Journal each year and help to promote
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herbalism and botanic medicine throughout Canada.
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THE SOCIETY HAS NO PAID OFFICIALS and is run entirely by
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volunteers from among the membership.
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Herbal Research Society BBS (416) 730-1702
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Canadian Herbal Research Society.
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P.O. Box 82. Stn. A.
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Willowdale, Ont. CANADA.
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M2N 5S7.
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(416) 730-8077
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