Research Publications on "Sho-saiko-to" (1990-2001)

 

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<28>

Authors

  Inoue M.  Shen YR.  Ogihara Y.

Institution

  Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Nagoya City

  University, Japan.

Title

  Shosaikoto (kampo medicine) protects macrophage function

  from suppression by hypercholesterolemia.

Source

  Biological & Pharmaceutical Bulletin.  19(4):652-4, 1996 Apr.

Abstract

  The feeding of cholesterol-enriched diet for 2 weeks was enough to reduce

  nitric oxide (NO), prostaglandin E(2) (PGE(2) and interleukin-1 (IL-1)

  productions in thioglycollate-elicited murine macrophages. Although not

  showing anti-hypercholesterolemic action against ICR mice,

  Shosaikoto, a Kampo medicine, partially prevented the

  reduction of NO and IL-1 productions induced by the feeding of

  cholesterol-enriched diet, and completely released the reduction of PGE(2)

  production. These data suggest that the malfunction of macrophage induced by

  hypercholesterolemia may contribute to early atherogenesis and that

  Shosaikoto retains macrophage function to prevent the

  development of atherosclerosis, even though serum cholesterol is markedly

  increased.

 

<29>

Authors

  Shen YR.  Inoue M.  Nagatsu Y.  Ogihara Y.  Aburada M.

Institution

  Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Nagoya City

  University, Japan.

Title

  Anti-hyperlipidemic and anti-atherosclerotic actions of

  shosaikoto (kampo medicine).

Source

  Biological & Pharmaceutical Bulletin.  19(9):1160-5, 1996 Sep.

Abstract

  We investigated the anti-atherosclerotic action shown by

  Shosaikoto, a Kampo medicine, using hypercholesterolemic

  mice. Oral administration of Shosaikoto significantly

  suppressed the elevation of serum cholesterol in C57BL/6 mice fed a 1.25%

  cholesterol-enriched diet for four weeks and improved the T cell ratio in

  peripheral blood, which decreased with the increase of the serum cholesterol

  level. In addition, Shosaikoto reduced the accumulation of

  cholesteryl oleate, which alters macrophages into foam cells, after the

  treatment of macrophages with oxidized or acetylated low density lipoprotein

  (LDL). Enzymatic study revealed that the treatment of macrophages with

  oxidized LDL enhanced acyl-coenzyme A: cholesterol acyltransferase (ACAT)

  activity and markedly reduced neutral cholesteryl ester hydrolase (NCEase)

  activity. Shosaikoto treatment prevented a decrease in the

  NCEase activity, however due to the oxidized LDL treatment, although it

  slightly augmented ACAT activity. Thus, Shosaikoto, which is

  known to modulate the immune system, improves macrophage and lymphocyte

  functions diminished by hypercholesterolemia, resulting in an

  anti-atherosclerotic action.

 

<30>

Authors

  Ishizaki T.  Sasaki F.  Ameshima S.  Shiozaki K.  Takahashi H.  Abe Y.  Ito

  S.  Kuriyama M.  Nakai T.  Kitagawa M.

Institution

  Third Department of Internal Medicine, Fukui Medical School, Japan.

Title

  Pneumonitis during interferon and/or herbal drug therapy in patients with

  chronic active hepatitis.

Source

  European Respiratory Journal.  9(12):2691-6, 1996 Dec.

Abstract

  We report four cases of acute pneumonitis due either to interferon, or a

  herbal drug, "Sho-saiko-to", or both in combination, in

  patients with chronic active hepatitis, focusing on its pathogenesis and

  response to prednisolone therapy. These cases shared common clinical

  features: fever, dry cough, dyspnoea, hypoxaemia, diffuse infiltrates both on

  chest radiography and chest computed tomography, restrictive pulmonary

  functional impairment, and alveolitis on examination of transbronchial lung

  biopsy, all of which suggest acute interstitial pneumonia. Furthermore,

  lymphocytosis was observed in association with the dominant CD8+ T-cell

  subset in bronchoalveolar lavage fluid. A lymphocyte stimulation test using

  peripheral blood was positive to interferon in one case and to

  Sho-saiko-to in another. All patients responded to oral

  prednisolone therapy. Peripheral soluble interleukin-2 receptor levels

  decreased in parallel with improvement in the clinical course. All patients

  were free of symptoms with a follow-up of 1-3 yrs. We conclude that

  interferon- and/or Sho-saiko-to-induced acute pneumonitis

  may be due to allergic-immunological mechanisms rather than toxicity, and

  that peripheral levels of soluble interleukin-2 receptor appear to be good

  markers of disease activity.

 

<31>

Authors

  Sakaguchi S.  Furusawa S.  Yokota K.  Sasaki K.  Takayanagi M.  Takayanagi Y.

Institution

  First Department of Hygienic Chemistry, Tohoku College of Pharmacy, Sendai,

  Japan.

Title

  Effects of antitumor activity and protection of shock symptoms by a

  traditional Chinese medicine (sho-saiko-to) in recombinant

  human tumor necrosis factor administered mice.

Source

  Biological & Pharmaceutical Bulletin.  19(11):1474-8, 1996 Nov.

Abstract

  The effects of a traditional Chinese medicine Sho-saiko-to

  (Kampo prescription) were investigated on the various metabolic disorders and

  antitumor activity of recombinant human tumor necrosis factor (rhTNF)

  administered to mice. The glycogen level in liver of rhTNF (5 x 10(4)

  units/mouse, i.v.)-injected mice was markedly lower at 4 h post-intoxication

  than that in the control, whereas the administration of rhTNF to

  Sho-saiko-to (500 mg/kg/d, p.o.)-pretreated mice resulted in

  a greater level of glycogen than that in rhTNF alone-treated mice. In mice

  pretreated with Sho-saiko-to, the level of fibrinogen 4 h

  after rhTNF injection markedly increased as compared to that in mice treated

  with rhTNF alone. We also estimated the NO2 in murine macrophage cell line

  J774A.1 using mice serum after administration of

  Sho-saiko-to. Our results clearly demonstrated that J774A.1

  cells stimulated with endotoxin (1 micrograms/ml) and rhTNF (1 x 10(4)

  units/ml) can effectively produce nitric oxide (NO), and ascertained the

  suppressive effect of Sho-saiko-to (500 mg/kg/d,

  p.o)-pretreated serum on NO generation by endotoxin/TNF-activated J774A.1

  cells. When the cells were incubated with endotoxin/TNF and

  Sho-saiko-to pretreated serum (10-100 microliters), the NO

  level was significantly lower than that in control serum incubated with

  endotoxin/TNF alone. The effect of Sho-saiko-to (1 and 10

  micrograms/ml) on in vitro cytotoxicity by rhTNF in Meth-A Sarcoma cells was

  observed to be in a dose dependent fashion. In addition, there was a

  remarkable enhancement of antitumor activity of rhTNF by

  Sho-saiko-to pretreatment in mice. These findings suggest

  that the Kampo prescription Sho-saiko-to may protect mice

  from severe shock syndrome by rhTNF, and that it may enhance rhTNF-induced

  activity.

 

<32>

Authors

  Inoue M.  Shen YR.  Ogihara Y.

Institution

  Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Nagoya City

  University, Japan.

Title

  Restorative effect of shosaikoto (kampo medicine) on

  diminution of nitric oxide synthesis in murine peritoneal macrophages induced

  by hypercholesterolemia.

Source

  Biological & Pharmaceutical Bulletin.  19(11):1468-73, 1996 Nov.

Abstract

  Macrophages play important roles both in immune response and in lipid

  metabolism and contribute to the development of atherosclerosis. To clarify

  the mechanism by which Shosaikoto, a Kampo medicine, shows

  anti-atherosclerotic action, we studied its effect on macrophage function.

  The production of nitric oxide (NO), prostaglandin E2 and interleukin 1 by

  macrophages in mice was reduced by feeding of a cholesterol-enriched diet,

  and the reduced production was observed 1 week after the beginning of

  cholesterol feeding. Furthermore, although oxidized low density lipoprotein

  (LDL) and lysophosphatidylcholine (LPC) reduced NO production, macrophages

  prepared from mice treated with Shosaikoto at a dose of 1.2

  g/kg/d restored the reduced NO production by them as well as by

  hypercholesterolemia. When the content of LPC was measured, no difference was

  observed between mice fed a cholesterol-enriched diet in the presence or

  absence of Shosaikoto treatment, suggesting that the

  restorative effect of Shosaikoto is not due to the

  inhibition of LPC production or accumulation. Conclusively,

  Shosaikoto prevents the modification of macrophage function

  induced by atherogenic factors, which is probably linked to its displayed

  anti-atherosclerotic action.

 

<33>

Authors

  Yamaoka Y.  Kawakita T.  Kaneko M.  Nomoto K.

Institution

  Kampo (Traditional Chinese Medicine) Research Laboratory, Kanebo Co., Ltd.,

  Osaka, Japan.

Title

  A polysaccharide fraction of Zizyphi fructus in augmenting natural killer

  activity by oral administration.

Source

  Biological & Pharmaceutical Bulletin.  19(7):936-9, 1996 Jul.

Abstract

  Shosaiko-to (Xiao-chai-hu-tang, SHO), a Kampo medicine, was

  prepared by decocting a prescription of 7 kinds of crude drugs, namely

  Bupleuri Radix, Pinelliae Tuber, Scutellariae Radix, Zizyphi Fructus, Ginseng

  Radix, Glycyrrhizae Radix and Zingiberis Rhizoma. Previously, we reported

  that the effect of the orally administered SHO in augmenting natural killer

  (NK) activity in the peripheral blood was attributed to the acidic

  polysaccharide fraction. To characterize the active components in the crude

  materials in SHO, the effects of extracts and various fractions were

  investigated by oral administration. The extracts of Zizyphi Fructus,

  Zingiberis Rhizoma, Scutellariae Radix, Glycyrrhizae Radix and Pinelliae

  Tuber augmented NK activity by oral administration. The high weight molecular

  fraction of Zizyphi Fructus was the most effective in augmenting NK activity.

  Thus, we obtained an active polysaccharide fraction from the high weight

  molecular fraction of Zizyphi Fructus. This polysaccharide fraction with a

  high molecular weight of approximately 43,000 contained 54.7% carbohydrate,

  61.8% uronic acid and 20.9% protein. The sugar moiety was composed of

  rhamnose, arabinose, xylose, fucose, mannose, galactose, glucose and

  galacturonic acid in molar ratios of 28:59:11:9:7:32:20:100.

 

<34>

Authors

  Inada K.  Yokoi I.  Kabuto H.  Habu H.  Mori A.  Ogawa N.

Institution

  Department of Neuroscience, Okayama University Medical School, Japan.

Title

  Age-related increase in nitric oxide synthase activity in senescence

  accelerated mouse brain and the effect of long-term administration of

  superoxide radical scavenger.

Source

  Mechanisms of Ageing & Development.  89(2):95-102, 1996 Aug 15.

Abstract

  The levels of nitric oxide (NO) and NO synthase (NOS) activities were

  compared in the brains of young adult (3 months old), aged (11 months old)

  and TJ-960 administered (11 months old) senescence accelerated mice (SAM), of

  which the SAMP8 substrain is inferior in acquisition of learning due to the

  abnormality of glutamatergic neurotransmission in the cerebral cortex.

  TJ-960, which is based on the Kampo (Japanese traditional herbal medicine)

  prescription Sho-saiko-to-go-keishi-ka-shakuyaku-to, acts as

  a superoxide radical scavenger and attenuates the deterioration of neuronal

  activity associated with aging. We administered TJ-960 orally for 5 months.

  In the cerebral cortex of aged SAMP8, NOS activity was increased compared

  with that of young adult SAMP8. Though TJ-960 did not alter the contents of

  NO in any brain region compared with those in aged SAMP8, it did prevent the

  increase in NOS activity in the aged cerebral cortex. Our data suggest that

  NOS activity may increase to compensate for the reduced sensitivity of the NO

  reaction system in the aging process, and that TJ-960 may normalize this

  increased NOS activity in the cerebral cortex, although further work is

  clearly needed to ascertain maintenance in the acquisition of learning.

 

<35>

Authors

  Komatsu M.  Hiramatsu M.  Yokoyama H.  Willmore LJ.

Institution

  Division of Medical Science, Institute for Life Support Technology, Yamagata

  Technopolis Foundation, Japan.

Title

  Effect of TJ-960 (a Japanese herbal medicine) on free radical changes within

  an iron-induced focal epileptogenic region in rat brain measured by in vivo

  L-band electron spin resonance.

Source

  Neuroscience Letters.  205(3):189-92, 1996 Mar 1.

Abstract

  In vivo L-band electron spin resonance (ESR) system was used to measure the

  decay of nitroxide radicals in the living rat cerebrum containing a cortical

  area with an iron-induced epileptogenic region. Carbamoyl-PROXYL

  (3-carbamoyl-2,2,5,5-tetramethyl-1-pyrrolinyloxy) was injected

  intraperitoneally. The decay of nitroxide radicals in the iron-injected

  regions at the subacute stage of epileptogenesis was prolonged. The Japanese

  herbal medicine, sho-saiko-to-go-keishi-ka- shakuyakuto

  (TJ-960), a compound known to have free radical scavenging activity,

  inhibited the delay of nitroxide radical decay in the rat cerebrum with an

  iron-induced epileptic focus following injection of carbamoyl-PROXYL. TJ-960

  did not affect the decay of nitroxide radicals in the control rats' brain.

  These data show that TJ-960 has the scavenging activity for free radicals

  generated within an iron-induced epileptogenic regions of rat brain.

 

<36>

Authors

  Shen YR.  Inoue M.  Ogihara Y.

Institution

  Department of Pharmacognosy, Nagoya City University, Japan.

Title

  Effect of Shosaikoto (Kampo medicine) on the adherence of

  monocytes in hypercholesterolemic rabbit.

Source

  Biological & Pharmaceutical Bulletin.  19(1):149-52, 1996 Jan.

Abstract

  Monocytes/macrophages are known to be involved in atherogenesis, and the

  adherence of monocytes to the endothelium is considered an earliest

  characteristic of atherogenesis. Therefore, we studied the mechanism by which

  Shosaikoto, a Kampo medicine, shows anti-atherosclerotic

  action, which has been already shown in hypercholesterolemic rabbits.

  Hypercholesterolemia in rabbits gradually reduced the monocyte number in

  peripheral blood, whereas Shosaikoto treatment suppressed

  this decrease in circulating monocytes. Furthermore, although monocytes from

  hypercholesterolemic rabbits increased in adherence to endothelial cells even

  without lipopolysaccharide (LPS) activation, Shosaikoto

  treatment reduced the enhanced adherence observed in monocytes from

  hypercholesterolemic rabbits. These data suggested that the

  anti-atherosclerotic action shown by Shosaikoto resulted

  partly from the suppression of the enhanced adherence characteristic of

  hypercholesterolemia.

 

<37>

Authors

  Miyamoto K.  Lange M.  McKinley G.  Stavropoulos C.  Moriya S.  Matsumoto H.

  Inada Y.

Institution

  Division of Rheumatology, St. Luke's-Roosevelt Hospital Center, Columbia

  University, New York, NY 10025, USA.

Title

  Effects of sho-saiko-to on production of prostaglandin E2

  (PGE2), leukotriene B4 (LTB4) and superoxide from peripheral monocytes and

  polymorphonuclear cells isolated from HIV infected individuals.

Source

  American Journal of Chinese Medicine.  24(1):1-10, 1996.

Abstract

  The effects of Sho-saiko-to (SST), a traditional Chinese

  medicine, on the production of PGE2 from monocytes, LTB4 and superoxide from

  polymorphonuclear cells (PMNC) in HIV infected individuals were studied. SST

  inhibited the production of PGE2 from monocytes stimulated by opsonized

  zymosan in all groups including the healthy control group and also inhibited

  the production of superoxide from PMNC after stimulation with FMLP. On the

  other hand, SST enhanced the production of LTB4 when PMNC were stimulated by

  the calcium ionophore A23187. These results suggest that SST has different

  effects on the production of prostanoids or superoxide from monocytes and

  PMNC. Furthermore, our data indicates that inhibition of PGE2 or superoxide

  production will lead to indirect suppression of HIV, and enhancement of LTB4

  will contribute to the upregulation of the immune reaction in HIV infected

  individuals.

 

<38>

Authors

  Kimura Y.  Miwa H.  Furukawa M.  Mizukami Y.

Institution

  Department of Otolaryngology, Kanazawa University School of Medicine, Japan.

Title

  Relapsing polychondritis presented as inner ear involvement.

Source

  Journal of Laryngology & Otology.  110(2):154-7, 1996 Feb.

Abstract

  We report a rare case of relapsing polychondritis with an initial symptom of

  inner ear involvement. This 53-year-old Japanese man experienced a hearing

  difficulty, tinnitus in both ears, and dizziness of sudden onset, but lacked

  auricular chondritis at that time, which is the most frequent finding in

  relapsing polychondritis. Thus it was difficult to reach a correct diagnosis.

  Steroid therapy, with oral prednisolone 15 mg daily, was effective. Almost

  two months after we began the steroid therapy, the patient complained of

  losing interest in his work and reported a hallucination vision on the TV

  screen, so the dose of prednisolone was decreased to 10 mg. The

  hallucinations then disappeared, but the serum level of C-reactive protein

  increased highly. To reduce the dose of prednisolone, we tried low-dose oral

  methotrexate. However, we had to discontinue it when the patient experienced

  severe vomiting and diarrhoea. As adjuvant therapy, we then administered

  Sho-saiko-to, Chinese herbal medicines with few side

  effects. Symptoms and laboratory abnormalities then improved markedly.

 

<39>

Authors

  Yamashiki M.  Nishimura A.  Nomoto M.  Suzuki H.  Kosaka Y.

Institution

  Department of Laboratory Medicine, Mie University School of Medicine,

  University of Pittsburgh, Pennsylvania, USA.

Title

  Herbal medicine 'Sho-saiko-to' induces tumour necrosis

  factor-alpha and granulocyte colony-stimulating factor in vitro in peripheral

  blood mononuclear cells of patients with hepatocellular carcinoma.

Source

  Journal of Gastroenterology & Hepatology.  11(2):137-42, 1996 Feb.

Abstract

  'Sho-saiko-to' (TJ-9) is a Japanese herbal medicine that is

  commonly administered to patients with chronic viral liver disease in order

  to improve their overall physical condition and to prevent the development of

  liver cancer, The present in vitro study demonstrated that, by adding TJ-9 to

  cell cultures, there were dose-dependent increases in production levels of

  tumour necrosis factor-alpha (TNF-alpha) and granulocyte colony-stimulating

  factor (G-CSF) in peripheral mononuclear cells of patients with

  hepatocellular carcinoma accompanied by liver cirrhosis. Increases in the

  production of TNF-alpha and G-CSF in control cell cultures exposed to

  different herbal medicines were low, and this indicates the specificity of

  the response increases in production of these cytokines to TJ-9. TNF-alpha

  and G-CSF are known to play important roles in the biological defence

  mechanism. Administration of TJ-9 may, therefore, be beneficial for patients

  afflicted with intractable liver diseases because it could mildly induce

  these cytokines.

 

<40>

Authors

  Matsuzaki Y.  Kurokawa N.  Terai S.  Matsumura Y.  Kobayashi N.  Okita K.

Institution

  First Department of Internal Medicine, Yamaguchi University School of

  Medicine, Japan.

Title

  Cell death induced by baicalein in human hepatocellular carcinoma cell lines.

Source

  Japanese Journal of Cancer Research.  87(2):170-7, 1996 Feb.

Abstract

  We examined the action of baicalein, a flavonoid contained in the herbal

  medicine sho-saiko-to (TJ-9), on three cell lines of human

  hepatocellular carcinoma (HCC). Treatment with baicalein strongly inhibited

  the activity of topoisomerase II and suppressed the proliferation of all

  three HCC cell lines. But the mode of cell death induced by baicalein

  differed according to the cell line. Baicalein induced apoptosis in a

  concentration-dependent manner in only one cell line, and an increased

  concentration of baicalein produced cell death via necrosis in the other two

  lines. These results suggest that the inhibition of topoisomerase II is not

  by itself sufficient for induction of apoptosis, and that there is a more

  important mechanism which can account for the difference in susceptibility of

  cells to apoptosis induced by baicalein.

 
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