Patents
Literature
Patsnap Eureka AI that helps you search prior art, draft patents, and assess FTO risks, powered by patent and scientific literature data.

21 results about "Cardioprotection" patented technology

Cardioprotection includes all mechanisms and means that contribute to the preservation of the heart by reducing or even preventing myocardial damage. Cardioprotection encompasses several regimens that have shown to preserve function and viability of cardiac muscle cell tissue subjected to ischemic insult or reoxygenation. Cardioprotection includes strategies that are implemented before an ischemic event (preconditioning, PC), during an ischemic event (perconditioning, PerC) and after the event and during reperfusion (postconditioning, PostC). These strategies can be further stratified by performing the intervention locally or remotely, creating classes of conditioning known as remote ischemic PC (RIPC), remote ischemic PostC and remost ischemic PerC. Classical (local) preconditioning has an early phase with an immediate onset lasting 2–3 hours that protects against myocardial infarction. The early phase involves post-translational modification of preexisting proteins, brought about by the activation of G protein-coupled receptors as well as downstream MAPK's and PI3/Akt. These signaling events act on the ROS-generating mitochondria, activate PKCε and the Reperfusion Injury Salvage Kinase (RISK) pathway, preventing mitochondrial permeability transition pore (MTP) opening. The late phase with an onset of 12–24 hours that lasts 3–4 days and protects against both infarction and reversible postischemic contractile dysfunction, termed myocardial stunning. This phase involves the synthesis of new cardioprotective proteins stimulated by nitric oxide (NO), ROS and adenosine acting on kinases such as PKCε and Src, which in turn activate gene transcription and upregulation of late PC molecular players (e.g., antioxidant enzymes, iNOS).

Cardiac protective lipids and methods of use

The present invention includes a method of reducing or eliminating cardiac toxic effects or cardiac pathological effects of one or more active agents comprising administering to a subject in need thereof an effective amount of one or more lipids that reduce or eliminate cardiac toxic effects of one or more active agents wherein the lipids have the formula: # imgabs0 #.
Owner:SIGNPATH PHARMA INC

Traditional Chinese medicine composition for treating acute myocardial infarction, pharmaceutical preparation and application thereof

The invention discloses a traditional Chinese medicine composition for treating acute myocardial infarction, a pharmaceutical preparation and application thereof and belongs to the technical field of traditional Chinese medicine. The traditional Chinese medicine composition is prepared from, by weight, 9-18 parts of ginseng, 3-6 parts of pseudo-ginseng, 9-18 parts of ligusticum wallichii, 12-24 parts of radix achyranthis bidentatae, 6-12 parts of fructus forsythiae and 9-18 parts of radix curcumae. Compared with the prior art, the traditional Chinese medicine composition disclosed by the invention has the beneficial effects that (1) the traditional Chinese medicine composition provided by the invention can reduce the myocardial infarction area after ischemia, inhibit myocardial fibrosis and improve heart structure and function changes caused by acute ischemic injury; and (2) the traditional Chinese medicine composition provided by the invention can effectively inhibit oxidative stress reaction and relieve mitochondrial injury, thereby playing a role in protecting the heart. And (3) the traditional Chinese medicine composition has the advantage of good safety and can be taken for a long time.
Owner:XIYUAN HOSPITAL OF CHINA ACAD OF CHINESE MEDICAL SCI

Proteins with cardioprotective activity

A protein selected from the group consisting of Chrdl1, Fam3c, Fam3b and a fragment thereof, or a polynucleotide encoding therefor, for use in treating or reducing the risk of heart disease.
Owner:INT CENT FOR GENETIC ENG & BIOTECH

Compound composition for enhancing heart protection function of NMN by small molecule peptide

The invention relates to the technical field of biological medicine, in particular to a compound formula capsule for enhancing the heart protection function of NMN through small molecule peptide. The active ingredients of the capsule comprise NMN and specific small molecule peptides shown in SEQ NO 01-05, and the mass ratio of the NMN to the specific small molecule peptides shown in SEQ NO 01-05 is 7: 1.5: 1.5: 1.5: 1.5: 1.5. The five small molecule peptides respectively contain basic / acidic amino acids, Gly-Pro structures, disulfide bonds and other characteristic sequences and are prepared through solid-phase synthesis or recombinant expression, and the purity is greater than or equal to 95%. A capsule carrier is gelatin or plant cellulose, auxiliary materials comprise microcrystalline cellulose and magnesium stearate, a dry granulation process is adopted, particles with the particle size of 80-120 meshes are prepared, the filling amount of each particle is 0.5 g, and the disintegration rate in simulated intestinal juice within 1 hour is larger than or equal to 85%. The formula can form a uniform dispersion system, and is suitable for various dosage forms such as capsules, tablets and the like.
Owner:BEIJING ZHICHOU TECHNOLOGY CO LTD

Lispiraceae exosome as well as preparation method and application of Lispiraceae exosome

The invention belongs to the technical field of biology, and particularly relates to a hispidobium exosome as well as a preparation method and application of the hispidobium exosome. The application is the application of the hispidobium exosome in preparation of medicines for treating myocardial infarction. The hispidobium exosome provided by the invention has a heart protection effect and can effectively relieve myocardial infarction, meanwhile, the preparation method is simple and easy to control, in addition, the hispidobium source is wide, and the sustainability of exosome preparation is ensured. Therefore, the trichospirillum exosome is expected to become a safe and effective new strategy for treating myocardial infarction.
Owner:CHINA AGRI UNIV

Pharmaceutical compositions suitable for intravenous administration

This invention is directed to compositions comprising bisantrene, particularly formulations of bisantrene dihydrochloride, wherein the formulations are suitable for intravenous administration into peripheral veins as well as methods for their use and methods for preparation of such compositions. The compositions according to the present invention eliminate the need to administer bisantrene by central venous catheter administration. The compositions can be used to treat malignancies and other conditions, and may be used for cardioprotection in patients undergoing chemotherapy with anthracycline-based anti-neoplastic agents. The inclusion of α-hydroxy acids in compositions according to the present invention improves the stability of such compositions and prevents precipitation of the bisantrene.
Owner:RACE ONCOLOGY LTD

Application of naringenin in preparation of medicine for preventing and treating tacrolimus-induced cardiotoxicity

The invention discloses application of naringenin in preparation of a medicine for preventing and treating cardiotoxicity induced by tacrolimus. The naringenin disclosed by the invention is a natural active matter, is non-toxic to cells, and has a potential heart protection effect of reversing, preventing and treating tacrolimus-induced cardiotoxicity; naringenin reduces expression of Cav1.2 on a membrane so as to influence a calcium signal channel and reverse calcium overload and cell apoptosis caused by tacrolimus; cav1.2 can be used as a target spot for preventing and treating cardiotoxicity induced by FK506, and the invention also prompts that overload calcium can be treated by using a corresponding calcium chelating agent, so that a theoretical basis is provided for the naringenin as a potential auxiliary medicine for tacrolimus application; the further deep research is expected to be beneficial to deep understanding of the action mechanism of the naringenin and provide more support for clinical application of the naringenin.
Owner:NANJING NORMAL UNIVERSITY

Compositions and methods for treating ischemic heart disease

The present disclosure is directed to the treatment of ischemic heart disease and clinical conditions associated with ischemic heart disease. A composition containing a monoclonal antibody directed against gastric inhibitory polypeptide is administered. This results in cardioprotective effects against acute myocardial infarction, such as a decrease in circulating triglycerides, total cholesterol, and low-density lipoproteins, and an increase in the ratio of high-density lipoprotein to total cholesterol.
Owner:METROHEALTH VENTURES LLC

Method for screening anti-inflammatory cardiac protection active components of Siji decoction

PendingCN121856432ADefining anti-inflammatory cardioprotective effectsComponent separationCardioprotectionMetabolite
The invention discloses a method for screening anti-inflammatory heart protection active components of Siji decoction. The method comprises the following steps: 1, finding eicosanoic acid related to the drug effect of the Siji decoction and measuring the content of eicosanoic acid; 2, identification of components absorbed into blood by the Siji decoction and determination of relative peak intensity; and 3, analyzing the correlation between the content of the eicosanoic acid metabolite related to the drug effect of the Siji decoction and the relative peak intensity of the component absorbed into blood by the Siji decoction, and screening the anti-inflammatory heart protection active component of the Siji decoction. The method comprises the following steps: by taking an eicosanoic acid metabolic profile as a drug effect target, constructing a correlation model of quantitative information of eicosanoic acid metabolites in a rat with heart failure at different time points and blood-entering component intensities of Siji decoction at different time points; through screening, it is determined that the four components of songorine, neoline, talasamine and isoliquiritigenin have the definite anti-inflammatory heart protection effect, and the method is accurate and efficient.
Owner:FOURTH MILITARY MEDICAL UNIVERSITY

Methods of treating fibrosis and arrhythmia with a neuregulin-1 fusion protein

The present invention relates to a recombinant fusion protein comprising a fragment of the cardioprotective protein neuregulin-1 (NRG-I) fused to a HER3 monoclonal antibody (mAb) backbone and to a method of treating atrial fibrillation and / or cardiac fibrosis in a subject in need thereof comprising administering a therapeutically effective amount of the recombinant fusion protein or the pharmaceutical composition comprising the recombinant fusion protein disclosed herein.
Owner:SALUBRIS BIOTHERAPEUTICS INC

Application of cornua cervi pantotrichum tissue-derived exosome-like nanoparticles in preparation of medicine for preventing and treating senile cardiovascular diseases

The invention discloses application of cornua cervi pantotrichum tissue-derived exosome-like nanoparticles in preparation of a medicine for preventing and treating senile cardiovascular diseases. A sterile, stable and high-purity cornua cervi pantotrichum tissue exosome is obtained by adopting an enzyme digestion-differential centrifugation-ultra-high-speed centrifugation combined method, the physiological efficacy of the cornua cervi pantotrichum tissue exosome in heart protection is studied, and it is found that the cornua cervi pantotrichum tissue exosome can significantly improve cardiac dysfunction of acute aging mice induced by D-galactose (D-Gal). The cardiac ejection function, the cardiac fibrosis and the inflammation invasion level are remarkably improved. The compound has treatment potential in preparation of medicines for preventing heart protection and treating heart diseases, and provides a new strategy and a treatment method for treating cardiovascular diseases of old people.
Owner:XINJIANG UNIVERSITY

Cardioprotective compositions and methods for atrial fibrillation

PCT designated stage expiredWO2025155918A1Peptide/protein ingredientsGenetically modified cellsHeart cellsCells heart
The present technology provides compositions and methods for gene therapy and / or cell therapy for treatment of heart diseases, e.g., atrial fibrillation. In particular, the present technology provides transgenes, expression cassettes, vectors, recombinant AAV (rAAV) viral genomes, rAAV viruses or virions, and pharmaceutical compositions for overexpressing synaptopodin 2 like (SYNPO2L), isoform A (SYNPO2LA) in a cardiac cell in a subject, as well as methods of using the same in the prevention or treatment atrial fibrillation.
Owner:TENAYA THERAPEUTICS INC

Cardioprotective heart disease therapies

The present disclosure relates to compositions and methods for the treatment or prevention of heart disease (e.g., cardiomyopathy) in a subject. In some aspects, the present disclosure relates to vectors encoding, and compositions comprising, a therapeutic gene product, such as an MMP11 polypeptide, SYNPO2L polypeptide, or an oligonucleotide for inhibiting expression of MTSS1, that confers a cardioprotective effect, e.g., in a TTN mutant genetic background. The present disclosure also relates to the treatment of heart disease (e.g., cardiomyopathy, heart failure or related disorders) using such vectors or compositions.
Owner:TENAYA THERAPEUTICS INC

Method for analyzing vibration mode and weak interaction of veratric acid and derivatives thereof based on terahertz spectrum and DFT theory

Veratric acid is one of main benzoic acids separated from vegetables and fruits, and has certain anti-inflammatory activity. The vanillic acid is one of antioxidants from herbal medicines and fruits and has a heart protection effect as a phenolic compound, and the vanillic acid and the phenolic compound have similar molecular structures. The terahertz time-domain spectroscopy (THz-TDS) is used for measuring the absorption spectrum of the veratric acid and the vanillic acid in the range of 0.5-3.0 THz, the corresponding theoretical spectrum is calculated and predicted through the solid density functional theory (ss-DFT), and the absorption spectrum and the theoretical spectrum are highly matched. The vibration modes and weak interactions of veratric acid and vanillic acid are analyzed using a vibration mode automatic correlation determination method and an interaction area indicator (IRI), respectively. According to the method, THz-TDS and ss-DFT are combined, and the vibration mode and weak interaction of veratric acid and vanillic acid can be analyzed, so that reference is provided for future drug design.
Owner:GUILIN UNIV OF ELECTRONIC TECH

Substituted indole compounds as well as preparation method and application thereof

The invention discloses a polysubstituted indole compound as well as a preparation method and application thereof, and particularly relates to the field of medical chemistry, the structure of the polysubstituted indole compound is shown in a general formula I, and the definition of each substituent group is shown in the specification. The polysubstituted indole compound can be used for researching the MPO activity inhibition mechanism and can be used for preparing drugs for preventing and treating heart diseases. For myocardial H9c2 cells, the compound shows a concentration-dependent heart protection effect (Cpd.S1) at a low concentration (1-25 [mu] M), the protection effect is the strongest when the concentration is 25 [mu] M, and the cell survival rate reaches 66.19%. Therefore, the compound has good application prospect and value in treatment of heart diseases.
Owner:ANHUI MEDICAL UNIV