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65results about How to "Improve pathological damage" patented technology

Bifidobacterium adolescentis and application thereof

The invention relates to the technical field of microorganisms, and discloses bifidobacterium adolescentis and an application thereof. The collection number of the bifidobacterium adolescentis CCFM8630 is CGMCC No.14395. The bifidobacterium adolescentis CCFM8630 has the advantages that the level of neurotransmitter 5-hydroxytryptamine in peripheral blood of rats can be remarkably upgraded by the bifidobacterium adolescentis CCFM8630; the increased level of hormones such as testosterone in the peripheral blood of the rats due to high-glucose and high-fat diet and anomaly of abundance of Blautiaand Turicibacter in intestinal floras of the rats can be recovered; simulated gastrointestinal fluid can be tolerated, the bifidobacterium adolescentis can be quickly colonized in intestinal tracts,accordingly, rat livers with metabolic syndromes, pathological injury of duodenums and increase of the contents of triglyceride and total cholesterol in serum due to the high-glucose and high-fat dietand oral glucose tolerance can be remarkably improved, and the bifidobacterium adolescentis can be used for preventing, relieving or treating metabolic disorder such as the metabolic syndromes, irritable bowel syndromes and psychological illnesses such as anxiety and depression which are related to the metabolic syndromes.
Owner:INFINITUS (CHINA) CO LTD

Application of bifidobacterium adolescentis CCFM1061 in preparation of functional microbial agents, foods and/or medicines

ActiveCN110354148AImprove fasting blood sugarImprove Total Cholesterol ElevationMetabolism disorderUnknown materialsBifidobacterium adolescentisPerfluorooctanoic acid
The invention discloses application of bifidobacterium adolescentis CCFM1061 in preparation of functional microbial agents, foods and / or medicines. The bifidobacterium adolescentis CCFM1061 can be rapidly colonized in the intestinal tracts, can remarkably improve fasting blood glucose and oral glucose tolerance of type 2 diabetes induced by STZ and high-fat diet and decrease the area under a curvewhen glucose tolerance is reduced, can remarkably alleviate the increase of total cholesterol and the decrease of high-density lipoprotein cholesterol in serum of the type 2 diabetes caused by STZ and high-fat diet, can remarkably alleviate the insulin resistance of the type 2 diabetes, can remarkably improve the level of inflammation in liver tissues of the type 2 diabetes, and can remarkably alleviate the pathological damage of the pancreas, liver and other tissues of the type 2 diabetes. In addition, the bifidobacterium adolescentis CCFM1061 has strong adsorption capacity on perfluorooctanoic acid (PFOA), and has the capacity of relieving PFOA toxicity.
Owner:JIANGNAN UNIV

Application of inhibitor of histone deacetylase HDAC 6 in preparing drugs for preventing and treating acute kidney injury

The invention provides an application of inhibitor of histone deacetylase HDAC 6 in preparing drugs for preventing and treating acute kidney injury. Furthermore, the histone deacetylase HDAC 6 is Tubastatin A. The selective inhibitor of HDAC 6 can lighten the renal pathology damage of acute kidney injury induced by cis-platinum and improve the kidney function. The HDAC6 inhibitor TA can lower the release of inflammatory factors and lighten the oxidative stress reaction through regulating an AKT signal access, an NF-KB inflammation access, an autophagy level and an E-cadherin expression; thus the apoptosis of kidney tubule cell and necrosis of tubule expansion are reduced, the renal pathology damage and kidney function are improved; the inhibitor can protect the kidney structure and function in the acute kidney injury. Therefore, HDAC6 is likely to be an important target point to prevent and treat the acute kidney injury.
Owner:SHANGHAI EAST HOSPITAL

Traditional Chinese medicine composition for treating diabetic nephropathy and application thereof

The invention relates to a traditional Chinese medicine composition for treating diabetic nephropathy. The traditional Chinese medicine composition is prepared from the following raw material medicines in parts by weight: 25-35 parts of astragalus membranaceus, 15-25 parts of cordyceps cicadae, 8-12 parts of taxus chinensis, 1-5 parts of saffron, 10-15 parts of Chinese wolfberry, 10-20 parts of lucid ganoderma, 15-25 parts of radix puerariae, 15-25 parts of gynostemma pentaphylla, 10-20 parts of wine-treated rhubarb and 3-9 parts of liquorice. The invention further provides an application of the traditional Chinese medicine composition. The traditional Chinese medicine composition disclosed by the invention has a very good protection effect on the kidney of a rat with diabetic nephropathy,and can effectively reduce kidney weight index, blood sugar, serum creatinine and urea nitrogen, reduce proteinuria and improve pathological injury of kidney tissues of the rat with diabetic nephropathy. According to the application disclosed by the invention, the effects of reducing proteinuria and protecting kidneys are achieved by down-regulating the expression of TGF-beta1, p-Smad2, p-Smad3 and alpha-SMA proteins in kidney tissues of DN rats.
Owner:SHANGHAI PUDONG NEW AREA PEOPLES HOSPITAL

Compound for treating pneumonia and application thereof

The invention discloses a compound for treating pneumonia and application thereof, and relates to the technical field of medicines. The compound for treating pneumonia is a heterocyclic compound, a pharmaceutically acceptable salt of the heterocyclic compound and / or a pharmaceutically acceptable carrier of the heterocyclic compound. The compound for treating pneumonia has a significant improvementeffect on bacterial pneumonia, viral pneumonia, fungal pneumonia, immune pneumonia, mycoplasma pneumonia, chlamydia pneumonia and other pathogen pneumonia, and especially can significantly improve pathological damage of viral bacterial pneumonia. The heterocyclic compound involved in the compound for treating pneumonia is simple in synthesis method, is suitable for industrial production, and is more stable than natural analogues; the activity of the compound is remarkably superior to that of ribavirin, oseltamivir, cefazolin and penicillin G which are clinically first-line medicines, and theactivity of the compound is also remarkably superior to that of purine analogues A, B and C.
Owner:WEST CHINA HOSPITAL SICHUAN UNIV

Application of niclosamide ethanolamine salt in preparing diabetes type 1 treating medicines

The invention relates to a novel application of niclosamide ethanolamine salt, and in particular to the application of the niclosamide ethanolamine salt in preparing medicines for preventing and treating diabetes type 1 and complications thereof; and the invention also conducts studies on the protective effect and the action mechanism of the niclosamide ethanolamine salt on the diabetes type 1 and the complications thereof. Results show that the niclosamide ethanolamine salt can improve symptoms of polyuria, polydipsia and polyphagia in a mouse with the diabetes type 1, reduce blood glucose, glycosylated hemoglobin and urine glucose levels, increase a serum insulin level and improve pancreas pathological damage. In the aspect of protecting a kidney target organ, the niclosamide ethanolamine salt can reduce a urinary albumin excretion rate, lower a creatinine clearance rate, diminish the area of glomerular vascular loops, reduce NAG and NGAL discharge in urine and inhibit activation of Akt / mTOR / 4E-BP1 signaling pathways in kidney tissues. In addition, the niclosamide ethanolamine salt can also take an obvious protecting effect on liver and achieve a significant improving effect on muscle functions. Therefore, the niclosamide ethanolamine salt has a significant protective effect on the diabetes type 1 and the complications thereof.
Owner:SHENZHEN TRADITIONAL CHINESE MEDICINE HOSPITAL

New application of isorhamnetin

The invention discloses a new application of isorhamnetin, and the new application means that isorhamnetin is taken as an active component for preparation of medicaments or health food for treating enteritis. Research results show that: isorhamnetin is capable of obviously improving symptoms such as body weight loss, bloody stools, colon shortening and tissue pathological damage and the like of ulcerative colitis mice, and inhibiting expression of colon tissue inflammatory cytokines TNF-alpha and IL-6. Therefore isorhamnetin can be taken as the active component expected to be developed as the medicaments or health food for treating enteritis, and especially is expected to be developed as medicaments or health food for treating ulcerative colitis.
Owner:SHANGHAI UNIV OF T C M

Use of dencichine

The invention relates to the technical field of medicine, and especially relates to a use of dencichine. The invention discloses the use of dencichine, prodrugs and pharmaceutical salts or plant extracts containing dencichine in preparation of drugs or health-care products for prevention or treatment of ulcerative colitis. The dencichine disclosed for the first time can significantly improve the experimental ulcerative colitis mice weight reduction, bloody stool, shortening of colon, tissue pathological damage and other symptoms, provides a new choice for clinical treatment of ulcerative colitis, and has a good application prospect.
Owner:SHANGHAI UNIV OF T C M

Application of TRPV4 ion channel as drug target in organophosphorus compound poisoning

The invention discloses an application of a TRPV4 ion channel as a drug target in organophosphorus compound poisoning. A medicine is a TRPV4 inhibitor. The medicine comprises: pharmacological antagonists of TRPV4 including GSK2193874, HC-067047, GSK205, GSK3395879, RN-1734 and GSK2798745, a blocking type antibody of the TRPV4, siRNA of the TRPV4 and the like. The important point of the invention is that the TRPV4 is found to be closely related to brain injury caused by the organophosphorus compound poisoning; and the TRPV4 antagonists or the siRNA inhibits intracellular calcium flow caused bythe organophosphorus compound poisoning and NMDA receptor-mediated excitatory toxicity, so that the nervous system toxic effect induced by poisoning of two organophosphorus compounds including oxophosphorus and soman is remarkably reduced at both in-vivo and in-vitro levels. Therefore, the invention provides a new drug target for prevention and treatment of the organophosphorus compound poisoning,and provides a new strategy for clinical treatment of the organophosphorus compound poisoning.
Owner:ACADEMY OF MILITARY MEDICAL SCI

Application of bicyclol to preparation of diabetes drug

InactiveCN107115338ALower fasting blood sugar levelsImprove pancreatic histopathological damageMetabolism disorderHeterocyclic compound active ingredientsDrugDiabetes mellitus
Owner:INST OF MATERIA MEDICA AN INST OF THE CHINESE ACAD OF MEDICAL SCI

Application of phloretin to preparation of colitis preventing and treating drug

InactiveCN109364048AGain weightLower disease activity indexDigestive systemKetone active ingredientsDrugSide effect
The invention discloses an application of phloretin to preparation of an ulcerative colitis preventing and treating drug. According to the application of phloretin to the ulcerative colitis preventingand treating drug, the phloretin can prevent and treat ulcerative colitis, has no adverse reactions or side effects and has a maintained effect.
Owner:XINXIANG MEDICAL UNIV

Medicine for preventing and/or treating alcoholic intestinal injury

The invention discloses a medicine for preventing and / or treating alcoholic intestinal injury, and belongs to the technical field of microorganisms and medicines. The invention provides a medicine forpreventing and / or treating alcoholic intestinal injury or alcoholic liver injury. The effective component of the medicine is lactobacillus helveticus CCFM1121, and the effective component of the medicine is lactobacillus helveticus CCFM1121. The lactobacillus helveticus CCFM1121 can effectively relieve alcoholic intestinal injury and alcoholic liver injury, and is specifically embodied in that (1) the mRNA expression quantity of intestinal tight junction protein of an alcohol modeling mouse is remarkably increased; (2) the content of endotoxin (LPS) in serum of alcohol modeling mice is remarkably reduced; (3) the activity of glutamic-pyruvic transaminase (ALT) and glutamic oxalacetic transaminase (AST) in serum of alcohol modeling mice is remarkably reduced; and (4) the pathological injury of the liver tissue of the alcohol modeling mouse is obviously improved.
Owner:JIANGNAN UNIV

Drug for treating renal-deficiency humid-heat type chronic nephritis

The invention discloses a drug for treating renal-deficiency humid-heat type chronic nephritis. The drug is prepared from the following material medicines in parts by weight: 20-40 parts of astragalus membranaceus, 8-12 parts of white atractylodes rhizome, 8-12 parts of pulp of dogwood fruit, 10-30 parts of eucommia ulmoides, 10-20 parts of rhizoma alismatis, 10-30 parts of herba pyrrosiae, 10-30 parts of oldenlandia diffusa and 3-7 parts of pseudo-ginseng. After being proved by a pharmacological experiment, the drug disclosed by the invention has a better function in treating chronic nephritis, is safe to take, suitable for preventing and treating chronic nephritis. The invention further discloses a preparation method and an application of the drug.
Owner:NANJING HOSPITAL OF T C M

Product capable of regulating CYP1A1 gene expression

PendingCN111869879AImprove human gut healthHigh application prospectMilk preparationDigestive systemBacilliRegulator gene
The invention discloses a product capable of regulating CYP1A1 gene expression, and belongs to the technical field of microorganisms. The invention provides a product, the effective component of the product is Lactobacillus plantarum CCFM8661, and the Lactobacillus plantarum CCFM8661 can effectively regulone the human body CYP1A1 gene expression, which is specifically reflected in thon (1) ponhological damage of benzopyrene exposed mouse colonic tissue is significantly improved; (2) the mRNA expression level of the CYP1A1 gene in the colon of the mouse exposed by benzopyrene is remarkably improved, so that the product provided by the invention has an extremely high application prospect in regulating the expression of the CYP1A1 gene of a human body and improving the intestinal health of the human body.
Owner:JIANGNAN UNIV

Use of orientin

The invention relates to the technical field of medicine, and especially relates to a use of orientin. The invention discloses the use of orientin, prodrugs and pharmaceutical salts or plant extracts containing orientin in preparation of drugs or health-care products for prevention or treatment of ulcerative colitis. The orientin disclosed for the first time can significantly improve the experimental ulcerative colitis mice bloody stool, shortening of colon, tissue pathological damage and other symptoms, provides a new choice for clinical treatment of ulcerative colitis, and has a good application prospect.
Owner:SHANGHAI UNIV OF T C M
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