跳至主要内容

Microbiome-Lax May Relieve Constipation

 So great a need for constipation relief, so few constipation remedies. If only the estimated 4 million Americans who suffer from constipation had more options, particularly since dietary interventions so often fail. Additional options, new research suggests, may finally be on their way, in the form of genetically engineered probiotics.

According to researchers at the Mayo Clinic Center for Individualized Medicine, synthetic bacteria may spur the transit of food through the digestive system. The researchers add that synthetic bacteria may work better than generic probiotics, which don’t work for everyone because the gut microbiome – the community of bacteria found within the stomach and intestines – is unique to each person.

digestive system model

The synthetic bacteria produced by the Mayo scientists are genetically engineered to produce large amounts of the chemical tryptamine. These bacteria, the Mayo scientists report, “accelerated gastrointestinal transit” in a mouse model of constipation.

Medicilon can provide various animal models (including renal failure model, anemia animal model, gastric acid secretion animal model, and gastric ulcer model) to test drug effectiveness according to client needs. We can conduct tests on typical digestive system diseases, including gastric acid secretions, gastric ulcers, and renal failure, using rats as subjects.

Details of the scientists’ work appeared in the journal Cell Host & Microbe, in an article entitled “Gut Microbiota-Produced Tryptamine Activates an Epithelial G-Protein-Coupled Receptor to Increase Colonic Secretion.” This article describes how the scientists genetically engineered Bacteroides thetaiotaomicron, introduced colonies of this bacterium to colonoids from germ-free (GF) and humanized (ex-GF colonized with human stool) mice, and observed the physiologic effect of tryptamine in the gastrointestinal tract.

“…we show that the biological effects of tryptamine are mediated through the 5-HT4 receptor (5-HT4R), a G-protein-coupled receptor (GPCR) uniquely expressed in the colonic epithelium,” wrote the article’s authors. “Tryptamine increases both ionic flux across the colonic epithelium and fluid secretion in colonoids.”

Tryptamine helps food pass through the intestines with potentially less risk of side effects than other constipation drugs. “Tryptamine is similar to the chemical serotonin, which is produced in our gut,” said the article’s lead author Purna C. Kashyap, M.B.B.S., associate director of the Center for Individualized Medicine Microbiome Program.

The Mayo scientists determined that the tryptamine-induced effect is mediated by the 5-HT4 receptor, a G-protein-coupled receptor uniquely expressed in the colonic epithelium. When the 5HT4 receptor is activated by tryptamine, the cAMP level increases and fluid secretion is enhanced.

“In this study, we found tryptamine can activate a receptor in the mouse gut that normally responds to serotonin, causing increased secretion of fluid from the lining of the colon,” Dr. Kashyap explained. “Bacteria can direct the colon to secrete water via tryptamine acting on a host receptor in mice. This accelerates the movement of food through the digestive system.”

Bacterially produced tryptamine quickly degrades in the intestine and does not appear to increase in the bloodstream. That reduces the risk of side effects outside the gastrointestinal tract. Other drugs for constipation can affect different areas of the body, including the heart.

“Our goal with this research is to find treatments that act only in the GI tract without creating problems in other parts of the body,” Dr. Kashyap added.

The findings are also important to the study of gastrointestinal disorders such as irritable bowel syndrome.

Additional preclinical studies will be done to verify the findings. A clinical trial with humans is likely at least three years away, Dr. Kashyap indicated.

评论

此博客中的热门博文

What is preclinical testing?

In the process of  preclinical testing  of a compound or biological agent into a drug, the compound involved must go through the testing phase. First, we need to identify potential targets that can treat the disease. Then, a variety of compounds or preparations are screened out. Any compound that has shown potential as a drug for the treatment of this disease needs to be tested for toxicity before clinical testing to reduce the possibility of injury. preclinical testing What is the basis of preclinical testing? According to US Food and Drug Administration (FDA) regulations, a series of tests are required before a new drug is approved for use. In the first stage, basic research determines a hypothetical target for the treatment of a certain disease, and then screens small molecules or biological compounds to discover any substance with the potential to treat the disease. Then, a  preclinical research  phase followed, before which, as described above, the potential toxicity of the compou

Inventory of the three major in vitro pharmacokinetic research methods

  The metabolic properties of a compound are an essential factor in whether or not it can be used as a drug in the clinical setting, so pharmacokinetic studies of newly synthesized compounds are required in drug development. In vitro incubation with liver microsomes, recombinant CYP450 enzyme lines, and in vitro incubation with hepatocytes are some of the more common in vitro drug metabolism methods. 1. In vitro incubation method with liver microsomes The metabolic stability and metabolic phenotypes of candidate compounds in different species of liver microsomes are good predictors of the metabolic properties of compounds in vivo. They are practical tools for evaluating candidate compounds in the pre-development phase of drug development. Liver microsomes include rat liver microsomes, human liver microsomes, canine liver microsomes, monkey liver microsomes, and mouse liver microsomes. In in vitro incubation of the liver, microsomes are the "gold standard" for in vitro d

Enzyme Activity Assay Service

  Enzymatic assay Lance Assay Alphascreen Assay Z’-LYTE Assay Adapta Assay Kinase-Glo Assay ADP-Glo Assay Ligand Binding Assay ELISA Assay HTRF Assay Enzyme activity assays  are laboratory methods for measuring enzymatic activity. They are vital for the study of enzyme kinetics and enzyme inhibition. Enzyme units : Amounts of enzymes can either be expressed as molar amounts, as with any other chemical, or measured in terms of activity, in enzyme units. Medicilon provides various  enzyme activity assays  for  kinases , phosphatases, proteinases, deacetylase, peptidase, esterase, and other enzymes. Our line of well-characterized immunoassays and biochemical kits ensures accurate and reproducible results. Enzyme is a  large category of bio-molecules  that catalyze various biological processes including metabolic processes, cellular signaling and regulation, cell division and apoptosis. Enzymatic reactions convert substrate molecules into chemically modified molecules products with high sp