The present disclosure relates to the use of angiotensin II in therapeutic methods for the treatment of hypotension.

The present disclosure relates to the use of angiotensin II in therapeutic methods for the treatment of hypotension.

Provided herein are methods of stabilizing blood pressure in severe sepsis/septic shock and other types of distributive shock using TRPV1 agonists. Also provided are pharmaceutical formulations for increasing blood pressure in septic shock the formulation including at least one TRPV1 agonist in a dosage form for parenteral administration, wherein the TRPV1 agonist is selected from capsaicin, daphane TRPV1 agonists, vanillotoxin, N-oleoyl dopamine, N-arachidonyl dopamine, BrP-LPA, and derivatives and analogues thereof. Also provided are TRPV1 agonists co-lyophilized with adrenergic agonists and/or angiotensins in a dosage form for reconstitution and parenteral administration.

Provided herein are methods of stabilizing blood pressure in severe sepsis/septic shock and other types of distributive shock using TRPV1 agonists. Also provided are pharmaceutical formulations for increasing blood pressure in septic shock the formulation including at least one TRPV1 agonist in a dosage form for parenteral administration, wherein the TRPV1 agonist is selected from capsaicin, daphane TRPV1 agonists, vanillotoxin, N-oleoyl dopamine, N-arachidonyl dopamine, BrP-LPA, and derivatives and analogues thereof. Also provided are TRPV1 agonists co-lyophilized with adrenergic agonists and/or angiotensins in a dosage form for reconstitution and parenteral administration.

Subject matter of the present invention is an angiotensin-receptor-agonist and/or a precursor thereof for use in the treatment of a disease in a subject, ⋅wherein said disease is selected from the group comprising heart failure, chronic heart failure, acute heart failure (AHF), myocardial infarction (MI), stroke, liver failure, burn injuries, traumatic injuries, severe infection (microbial, viral (e.g. AIDS), parasitic diseases (e.g. Malaria)), SIRS or sepsis, cancer, acute kidney injury (AKI), CNS disorders (e.g. seizures, neurodegenerative diseases), autoimmune diseases, vascular diseases, hypotension and shock, and ⋅wherein said subject has an amount of DPP3 protein and/or DPP3 activity in a sample of bodily fluid that is above a predetermined threshold.

Subject matter of the present invention is an angiotensin-receptor-agonist and/or a precursor thereof for use in the treatment of a disease in a subject, ⋅wherein said disease is selected from the group comprising heart failure, chronic heart failure, acute heart failure (AHF), myocardial infarction (MI), stroke, liver failure, burn injuries, traumatic injuries, severe infection (microbial, viral (e.g. AIDS), parasitic diseases (e.g. Malaria)), SIRS or sepsis, cancer, acute kidney injury (AKI), CNS disorders (e.g. seizures, neurodegenerative diseases), autoimmune diseases, vascular diseases, hypotension and shock, and ⋅wherein said subject has an amount of DPP3 protein and/or DPP3 activity in a sample of bodily fluid that is above a predetermined threshold.

The invention relates to the pharmaceutical industry, particularly to the pharmaceutical industry related to biological drugs, biomacromolecules, biopharmaceuticals, or biologics. More particularly, the invention relates to a method for the manufacture of a highly controlled and stable dosage form with mucoadhesive properties for buccal administration of biologics such as lymphokines, hormones, hematopoietic factors, growth factors, antibodies, enzymes, inhibitors, vaccines, DNA, and RNA derivatives, among others. Based on inkjet printing, the invention uses inks comprising the biologic(s) included in a nanosystem, particularly in polymeric nanoparticles.

The present disclosures provides methods for decreasing injuries associated with intraoperative hypotension by intravenously administering to a subject a therapeutically effective amount of a fat emulsion, following a period of intraoperative hypotension and after the subject's mean arterial blood pressure has recovered. The disclosure also provides methods for preventing injuries associated with intraoperative hypotension, particularly for surgical candidates that have an increased risk for intraoperative hypotension. Non-limiting examples of injuries contemplated herein include myocardial injury, myocardial infarction, and acute kidney injury.

A medical composition for treatment of a peripheral vascular disease is provided. The medical composition may include a dosage of a GABA-a agonist, a dosage of an Angiotensin II modulator, and a dosage of a Direct Oral Anticoagulant. The Angiotensin II modulator may include at least one of an ARB and an ACE Inhibitor, the ARB being an Angiotensin II, type 1 receptor antagonist. A method for treating a patient with a microvascular disease condition is provided. The patient may be provided, the medical composition may be provided, and the medical composition may be administered. The step of providing the patient may include providing a patient with at least one of systemic sclerosis, vascular insufficiency, distal ischemia, COVID-19 infection, and sepsis.

A medical composition for treatment of a peripheral vascular disease is provided. The medical composition may include a dosage of a GABA-a agonist, a dosage of an Angiotensin II modulator, and a dosage of a Direct Oral Anticoagulant. The Angiotensin II modulator may include at least one of an ARB and an ACE Inhibitor, the ARB being an Angiotensin II, type 1 receptor antagonist. A method for treating a patient with a microvascular disease condition is provided. The patient may be provided, the medical composition may be provided, and the medical composition may be administered. The step of providing the patient may include providing a patient with at least one of systemic sclerosis, vascular insufficiency, distal ischemia, COVID-19 infection, and sepsis.