49 results about "Right ventricular hypertrophy" patented technology

In some aspects, the invention teaches pharmaceutical compositions that include a TGF-beta ligand trap, and methods of using a TGF-beta ligand trap to treat, prevent, or reduce the progression rate of pulmonary hypertension (PH). The invention also provides methods of using a TGF-beta ligand trap to treat, prevent, or reduce the progression rate of a variety of conditions including, but not limited to, pulmonary vascular remodeling, pulmonary fibrosis, right ventricular hypertrophy, diseases associated with excessive TGF-beta signaling, diseases associated with excessive GDF15 signaling, and diseases associated with excessive PAI-1 signaling. The invention further provides methods of using a TGF-beta ligand trap to reduce right ventricular systolic pressure in a subject.

The invention discloses application of hydroxysafflor yellow A in preparation of health care drugs or functional food for treating hypoxic pulmonary hypertension. The hydroxysafflor yellow A has the function of inhibiting pulmonary vascular structure remodeling and right ventricular hypertrophy caused by anoxia. The invention further relates to a method for extracting hydroxysafflor yellow A from traditional Chinese medicine safflower. According to the invention, a new technological means for researching and developing the safflower medicinal resource is provided, a research is made on the function of the effective component hydroxysafflor yellow A of safflower for inhibiting pulmonary hypertension, and the result indicates that the hydroxysafflor yellow A can effectively improve the pulmonary artery remodeling of hypoxic pulmonary hypertension rats and reduce pulmonary arterial pressure, so the hydroxysafflor yellow A is expected to be used in the prevention and treatment of pulmonary hypertension.

Methods are provided for preventing and treating pulmonary hypertension and right ventricular hypertrophy involving administering to a patient a caveolin peptide coupled to a cell permeating compound such as a cell permeating peptide.

The invention relates to novel pharmacological action of traditional Chinese medicine salvianolic acid A and application thereof in the preparation of products for preventing, relieving and/or treating pulmonary arterial hypertension and its complications. The salvianolic acid A has the advantages that the salvianolic acid A has the pharmacological action of relieving pulmonary circulation pressure rise, the pharmacological actions of relieving right heart failure due to pulmonary arterial hypertension, improving right ventricular hypertrophy and right ventricular enlargement, improving heart injury due to pulmonary arterial hypertension, and restoring from heart failure, and the pharmacological actions of lowering endothelin-1 level in pulmonary tissues, relieving pulmonary arterial remodeling and improving pathologic damage of pulmonary tissues; the salvianolic acid A is a monomer compound extracted from Salvia miltiorrhiza, has low toxicity, has a wide source range of material, has promising application and development prospect, is an ideal novel traditional Chinese medicine monomer for treating pulmonary arterial hypertension and its complications, and may be applied to prepare products for preventing, relieving and treating pulmonary arterial hypertension and its complications, such as chronic obstructive pulmonary emphysema, chronic pulmonary heart disease and heart failure.

Myocardial hypertrophy is a pathological change of a plurality of kinds of angiocardiopathy. The main mode is the heart remodeling comprising cardiac muscle cell hypertrophy and change of the interstitial tissue component mainly. In the present invention, the nitrate medicine is used in treatment for myocardial hypertrophy caused by various reasons and excellent therapy effect is obtained. Currently the nitrate medicine is extensively applied in treatment for the coronary heart disease, the heart colicky pain and heart failure. Preload of the heart and myocardial consumption of oxygen are reduced by extension of the venous system. The drugs used in clinical field currently comprise Nitroglycerin, Amyl Nitrite, dicho nitric acid sorbite, sorbide dinitrate, 5-isosorbide dinitrate, Nitroglycerin, pentanitrol ters and itramine tosylate.

The invention discloses a construction method of a diabetic cardiomyopathy animal model. An SD (Sprague Dawley) rat under high-sugar and high-fat feeding is subjected to multiple abdominal injection with STZ (streptozocin); after the diabetics diagnosis standard is reached, subcutaneous injection with isoprenaline is performed; after 2 weeks of continued feeding, left ventricular cannulation and three-lead electrocardiogram test of ventricular hemodynamic parameters and electrocardiogram parameters shows that the rat experiences cardiac dysfunction; heart weight index and left ventricular index show that the rat experiences evident ventricular hypertrophy; biochemical analysis on rat blood shows that the rat has evident myocardial damage; HE (hematoxylin-eosin) pathological staining satisfies pathological changes in diabetic cardiomyopathy; Masson collagen staining satisfies myocardial connective tissue proliferation of diabetic cardiomyopathy. The construction method has the advantages of good operational simplicity, short construction time, low mortality in construction phase, high construction success rate and the like, and the pathological process of myocardial damage due to human type 2 diabetes mellitus can be well simulated.

The invention provides application of icariin to the preparation of medicaments for preventing or treating pulmonary artery hypertension and complications thereof. The icariin can reduce pulmonary artery pressure and improve right ventricular hypertrophy, pulmonary heart disease and pulmonary vascular remodeling which are caused by pulmonary artery pressure increase.

The invention relates to a preparation method of saponin of radix adenophorae as well as an application of the saponin of radix adenophorae, which is prepared in accordance with technical scheme of the invention, in treating medicines for treating pulmonary arterial hypertension and related cardiovascular diseases caused by the pulmonary arterial hypertension. Based upon experimental studies, the saponin of radix adenophorae provided by the invention can take an obvious effect on reducing mean pulmonary arterial pressure (MPAP), right ventricle systolic pressure (RVSP) and right ventricular hypertrophy index (RVHI) of the pulmonary arterial hypertension. The saponin of radix adenophorae can be used for preventing and treating one or more diseases of special pulmonary arterial hypertension, heritable pulmonary arterial hypertension, drug and poison related pulmonary arterial hypertension, risk factor or disease related pulmonary arterial hypertension, pulmonary arterial hypertension caused by pulmonary veno-occlusive disease and (or) pulmonarycapillary hemangiomatosis, and neonatal persistent pulmonary arterial hypertension.

The present invention discloses uses of WNK kinase inhibitors in prevention and/or treatment of pulmonary hypertension, and particularly uses of WNK 463 in the prevention and / or treatment of pulmonary hypertension and complications thereof. Experiments by inventors of the present application find that the WNK kinase inhibitors (especially the WNK 463) show relatively good effects on protection of pulmonic circulation-right-heart pressure and function, right ventricular hypertrophy, etc. of monocrotaline (MCT)-induced pulmonary hypertension in rats, and have potential value of being developedinto drugs for the prevention and treatment of pulmonary hypertension and complications thereof.

The invention discloses a bisindole alkaloid compound as well as a synthesis method and application thereof. The compound has a structure as shown in formula I. In the formula I, R1 is independently selected from C1-C4 alkoxy or hydrogen; if R1 is alkoxy, n is 1 or 2; R2 is independently selected from C1-C4 alkyl groups or hydrogen; R3 is independently selected from a group consisting of C1-C4 alkoxy carbonyl groups or hydrogen; R4 is hydrogen; R5 is independently selected from a C1-C4 alkyl group or a C1-C4 hydroxyalkyl group; and R6 is independently selected from carbonyl, hydroxyl or hydrogen. The bisindole alkaloid compound can selectively relax pulmonary artery, inhibit proliferation of pulmonary artery endothelial cells and vascular smooth muscle cells, reduce right ventricular diastolic pressure of mice with pulmonary arterial hypertension and inhibit right ventricular hypertrophy. The bisindole alkaloid compound can resist drug addiction in a dose-dependent manner, has a chemical structure type different from that of an existing anti-addiction drug, and is expected to be developed into a novel anti-addiction drug.

The invention belongs to the field of medicinal chemistry and provides an application of ciglitazone in preparing drugs for treating pulmonary arterial hypertension. An experiment of the invention proves that ciglitazone is capable of effectively reducing average pulmonary artery pressure and pulmonary vasculature resistance of pulmonary arterial hypertension rats, increasing cardiac output, reducing right ventricular hypertrophy index, improving pulmonary vasculature remodeling and increasing protein expression of Gamma(peroxisome proliferation activated receptor, PPAR Gamma). The experimentproves that ciglitazone has a therapeutic effect on pulmonary arterial hypertension.

The invention discloses application of tetrahydrocannabivarinic in prevention and/or treatment of pulmonary arterial hypertension, and particularly relates to application of a composition containing tetrahydrocannabivarinic in prevention and/or treatment of pulmonary arterial hypertension and complications thereof. The tetrahydrocannabivarinic, especially a composition containing the tetrahydrocannabivarinic and other cannabinoid Cannabinoids, can significantly reduce right ventricular systolic pressure and right ventricular hypertrophy index of pulmonary arterial hypertension model mice, improve pulmonary edema and hepatic edema, can improve pulmonary arterial hypertension diseases, and especially, the combined administration can enhance the improvement effect on hepatic edema, and has important value for the development of drugs for treating pulmonary arterial hypertension.

The invention relates to a pulmonary hypertension marker and application thereof as a therapeutic target, in particular to the application of a NOC4L gene as the pulmonary hypertension marker and thetherapeutic target. The marker reveals the correlation between the NOC4L gene and pulmonary hypertension for the first time, uses NOC4L overexpression, NOC4L knockout mice and wild type mice to carryout continuous hypoxic environmental treatment, establishes a mouse pulmonary hypertension model, and finds that NOC4L gene overexpression significantly reduces a right ventricular systolic pressure,and significantly increases a right ventricular hypertrophy index and a pulmonary vascular remodeling rate, a right ventricular systolic pressure, a right ventricular hypertrophy index and a pulmonaryvascular remodeling rate of the NOC4L knockout mice. The marker provides a novel target for the research and development of novel drugs for the treatment of the pulmonary hypertension.

The invention discloses application of golden larch bark acetic acid in preparation of a medicine for treating pulmonary arterial hypertension. The invention belongs to the technical field of biological medicine. A pulmonary arterial hypertension disease mouse model is constructed through hypoxia (10%) induction. After the golden larch bark acetic acid is injected into the intraperitoneal cavity, the conditions of fur, diet, activity, death and the like of the pulmonary arterial hypertension mouse model are observed. Results show that the golden larch bark acetic acid (as shown in the formula I) has the effects of remarkably improving pulmonary vascular remodeling of animals with pulmonary hypertension, relieving right ventricular hypertrophy and right heart failure, improving the life quality of the animals with pulmonary hypertension (improving feeding and water inflow) and increasing the survival rate of the animals with pulmonary hypertension. Therefore, the golden larch bark acetic acid has a wide application prospect in the aspect of preventing and treating the pulmonary arterial hypertension disease.