Strong MIYARISAN® Probiotics, 90 tablets
- Item No: 831001A
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S$24.41
- Ex GST: S$22.39
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Strong
MIYARISAN® helps maintain gastrointestinal balance for
immune,
digestive and bowel movement health.
Accordingly,
it has established a role in:
·
Managing
constipation
·
Managing
diarrhoea
·
Preventing
antibiotic-associated diarrhoea
·
Managing
Irritable Bowel Disease (IBD)
·
Ameliorating
GI effects of H pylori eradication therapy
Rich Heritage of More Than 80 Years!
It provides the Clostridium butyricum Miyairi® 588 (CBM588®) strain which was first isolated by Dr Chikaji Miyairi in Japan’s Chiba Medical University in 1933.
Once
commercial production began in 1940, it was quickly adopted for use in various
Asian countries (Japan, Korea, and China) for managing diarrhoea and
constipation for more than 80 years now.
The safety of the CBM588® strain of Clostridium butyricum is well established. It is naturally found in the human gut, and it does not carry any genes encoding any toxins and virulence factors associated with Clostridium or other intestinal pathogens.
It is granted GRAS (Generally Regarded as Safe) status for use in US and as a novel food ingredient in EU. 1
Mode of Actions
CBM588® is resistant to stomach acid, heat, and antibiotics, allowing it to reach the intestines undenatured to proliferate.
During the process of proliferation, CBM588® produces butyric acid which brings about various beneficial effects:
1. It increases the abundance of Bifidobacterium, Lactobacillus, and Lactococcus species to improve the gut microbiome balance.2,5
2. Short-chain fatty acids such as butyric acid produced by CBM588® is used as an energy source for the intestinal lining’s epithelial cells and contribute towards strengthening the gastrointestinal barrier.2
3. It modulates inflammatory processes and the intestinal immune response, helping to maintain a stable intestinal environment.2
Application:
to prevent antibiotic-associated diarrhoea
CBM588® has been used to prevent antibiotic-associated diarrhoea in adults and children 3 as it plays an important role in controlling antibiotic-induced dysbiosis.
Specifically, was found to protect the gut mucin layer from the effects of antibiotic-induced dysbiosis. 4
And it promotes mucin production by modulating the gut microbiota. 5
As intestinal epithelial cells under the mucin layer contain absorptive epithelial cells, a dysfunction of these cells leads to diarrhoea induced by incomplete absorption of water in faeces. 6
The investigation of the immunological and metabolic interaction between our body and gut microbiome under antibiotic-induced dysbiosis revealed two novel protective mechanisms of epithelial cells in the colon under CBM588® treatment:
1. Inducing innate immune cells activity in the colonic lamina propria, thus enhancing gut epithelial barrier function.7
2.
Upregulating
anti-inflammatory lipid metabolites such as palmitoleic acid, 15d-prostaglandin
J2, and protectin D1 and reducing expression of inflammatory cytokines.
7
Diagram: Clostridium butyricum CBM588 promotes the thickness of the mucous layer and the integrity of the tight junctions thanks to the stimulation of the release of IL-17 exerted on the intraepithelial T cells, with a reduced permeability of pathogens and lipopolysaccharide. (↑ Increased, ↓ Decreased).
Application: Managing IBD
The gut immune system interacts with the gut microbiota and maintains intestinal homeostasis.
Accumulating evidence supports the idea that imbalance in this complicated network between the immune system and the microbiota is involved in the pathogenesis of gut inflammatory diseases, including IBD. 8
Interleukin 10 (IL-10) is a cytokine with potent anti-inflammatory properties that plays a central role in limiting host immune response, thereby preventing damage to the host and maintaining normal tissue homeostasis.
CBM588® ability to induce IL-10-producing immunoregulatory macrophages is being studied for its potential as an immunomodulatory probiotic for both maintenance and induction of remission in IBD, by targeting intestinal macrophages. 9,10
Application: Ameliorate GI Effects of H pylori Eradication Therapy
H pylori is deeply involved in gastroduodenal ulcer disease and H pylori-positive patients are generally treated using Triple Therapy with a proton pump inhibitor and two antibiotics selected from among the following three: amoxicillin, clarithromycin and metronidazole.
This therapy can achieve a bacterial eradication rate of about 80-90%.
But it also results in a high incidence of gastrointestinal side effects like diarrhoea and loose stools.
Studies
have shown that concomitant supplement with CBM588® during therapy reduced the
change in intestinal flora and prevented gastrointestinal side effects.11,12
Supplement Facts
Serving Size 3
Tablets |
|
Amount Per Serving |
|
Clostridium butyricum
MIYAIRI 588® (CBM588®) |
90 mg |
Other ingredients: lactose hydrate, corn starch, talc,
microcrystalline cellulose, magnesium stearate, sucrose. |
Dosage and Use
·
Take 1 tablet three times daily
after food. For use from 5 years and older.
Storage
Keep the bottle tightly closed in a cool and dry place away from direct sunlight. Refrigeration is recommended. Keep out of reach of children.
Product of Japan
Scientific
References:
1.
The
European Commission Commission Implementing Decision of 11 December 2014 authorising
the placing on the market of Clostridium butyricum (CBM 588) as a novel food
ingredient under Regulation (EC) No 258/97 of the European Parliament and of
the Council (notified under document C (2014) 9345) OJEU. 2014;57:153.
2.
Tadashi
A, Mao H, Motomichi T, Hiroshige M. Effect of Clostridium butyricum on
Gastrointestinal Infections. Biomedicines. 2022 Feb; 10(2): 483.
3.
Seki H. et al. Prevention
of antibiotic-associated diarrhea in children by Clostridium butyricum MIYAIRI.
Pediatr. Int. 2003; 45: 86-90
4.
Hagihara et al. The impact
of Clostridium butyricum MIYAIRI 588 on the murine gut microbiome and colonic
tissue. Anaerobe. 2018; 54: 8-18
5.
Hagihara
M., Yamashita R., Matsumoto A., Mori T., Inagaki T., Nonogaki T., Kuroki Y.,
Higashi S., Oka K., Takahashi M., et al. The impact of probiotic Clostridium
butyricum MIYAIRI 588 on murine gut metabolic alterations. J. Infect.
Chemother. 2019;25:571–577.
6. Merga Y., Campbell
B.J., Rhodes J.M. Mucosal barrier, bacteria and inflammatory bowel disease:
Possibilities for therapy. Dig. Dis. 2014;32:475–483.
7. Kanai, T., Mikami, Y.
& Hayashi, A. A breakthrough in probiotics: Clostridium butyricum regulates
gut homeostasis and anti-inflammatory response in inflammatory bowel disease. J
Gastroenterol 50, 928–939 (2015).
8. Sheehan D, Moran C,
Shanahan F. The microbiota in inflammatory bowel disease. J Gastroenterol.
2015. doi:10.1007/s00535-015-1064-1.
9. Okamoto T, Sasaki M,
Tsujikawa T, et al. Preventive efficacy of butyrate enemas and oral
administration of Clostridium butyricum M588 in dextran sodium sulfate-induced
colitis in rats. J Gastroenterol. 2000;35(5):341–6.
10. Hayashi A, Sato T,
Kamada N, et al. A single strain of Clostridium butyricum induces intestinal
IL-10-producing macrophages to suppress acute experimental colitis in mice.
Cell Host Microbe. 2013;13(6):711–22.
11. Shimbo I, Yamaguchi T,
Odaka T, et al. Effect of Clostridium butyricum on fecal flora in Helicobacter pylori eradication therapy. World J
Gastroenterol. 2005;11(47):7520–4.
12.
Kyoto I et al. Efficacy of Clostridium butyricum
preparation concomitantly with Helicobacter pylori eradication therapy in
relation to changes in the intestinal microbiota. Microbiol Immunol. 2008
Mar;52(3):156-61.
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