Use of angiotensin II (AII) receptor agonists to prevent or reduce hemodialysis-associated skeletal muscle cramps

Abstract

Disclosed herein is a therapeutic intervention to prevent, reduce, or treat hemodialysis-associated skeletal muscle cramps by administering All receptor agonists or other pharmacologic agents that augment homeostatic responses to hemodialysis while preventing derecruitment of skeletal muscle capillaries.

Claims

1. A method of preventing, reducing, or treating cramping during hemodialysis, said method comprising administering to a subject an effective amount of angiotensin II.

2. The method of claim 1, wherein the effective amount of angiotensin II is between 0.1 and 250 ng/kg of body weight of the subject.

Description

DESCRIPTION OF THE DRAWING

(1) FIG. 1 is a diagram showing the proposed pathogenesis of hemodialysis-associated skeletal muscle cramps and mechanism by which angiotensin II agonists can prevent them. Mannitol, saline, and hypertonic glucose are believed to work by reducing plasma volume contraction but undesirably increase solute load. No integrated pharmacologic rationale has been proposed for other interventions that have been attempted.

DETAILED DESCRIPTION OF THE INVENTION

(2) Muscle cramping during hemodialysis has been observed for several decades. These cramps are often severe, extremely unpleasant, and a leading cause of patient non-compliance to prescribed hemodialysis. In spite of this, there are no approved drug-based treatments for cramping during dialysis.

(3) The present invention features the insight that dialysis cramps can be prevented, reduced, or treated by angiotensin II agonists, such as angiotensin II itself. Without wishing to be bound by theory, it is believed that, because angiotensin II (AII) acts on postcapillary as well as precapillary resistances, it is able to increase peripheral vascular resistance while maintaining capillary patency. This provides an advantage over agents that activate the sympathetic nervous system, releasing norepinephrine, because such activation only effects precapillary resistances and results in capillary derecruitment. Concomitant activation of both the sympathetic nervous system and renin-angiotensin system can prevent capillary derecruitment during hemodialysis. Conversely, a further insight of the invention is that patients who cramp frequently during hemodialysis have a sympathetic nervous system response to this volume stress that is not modulated by concomitant renin-angiotensin response and this results in derecruitment of skeletal muscle capillaries and cramping. Without wishing to be bound by theory, it is likely that administration of exogenous AII agonists can augment blood pressure homeostasis during hemodialysis and that its dual action on precapillary as well as postcapillary resistances can modulate sympathetic nervous system responses, thereby preventing intradialytic skeletal muscle cramps.

(4) Further, the action of AII agonists which distinguishes them from the adrenergic agents employed to treat hemodialysis-associated hypotension also makes them a preferred treatment for this hemodialysis complication and for patients with septic and other forms of shock.

(5) Angiotensin II (AII) is an octapeptide having a molecular weight of 1046.2 Daltons and the following structure:
H-Asp-Arg-Val-Tyr-Ile-His-Pro-Phe-OH (SEQ ID NO:2)

(6) AII is the classical effector of the renin-angiotensin cascade and is formed endogenously from angiotensinogen by two successive hydrolytic reactions. Several AII polypeptide metabolites of AII also act on angiotensin receptors, and it is likely that small molecule agonists can also be developed and employed. AII is available commercially for clinical research as a sterile dry powder supplied in glass vials. It is intended to be administered intravenously after reconstitution in physiological saline.

(7) Although AII has been administered to human subjects both by injection and infusion, it is the prior experience with infusions that is most relevant to the current use of this agent. AII infusions generally have been used to probe physiological responses in normal subjects and in patients, but in a few instances have been administered as therapy to treat patients with septic shock that has become refractory to catecholamines, during cesarean section to maintain blood pressure during spinal anesthesia, and to deliver intra-arterial chemotherapy more selectively.

(8) Proposed Clinical Use of Angiotensin II (AII) and/or Other AII Receptor Agonists

(9) Depending on the specific application, angiotensin II will generally be administered as infusions to patients beginning at the start of hemodialysis and continuing through this procedure. It is convenient to administer these infusions through the injection port in the hemodialysis circuit that returns blood to the patient after passing through the dialyzer. An effective dose is 5 ng/kg.Math.min but this dose may have to be adjusted in individual patients. During administration, the dose may be increased if cramping occurs to maintain skeletal muscle capillary patency by preventing capillary derecruitment while augmenting blood pressure homeostatic mechanisms, or decreased to prevent excessive increments in blood pressure.

(10) Angiotensin II is superior to catecholamines to maintain blood pressure in patients who would otherwise suffer from hemodialysis-associated hypotension. Other angiotensin II agonists such as metabolites or orally active small molecules that are angiotensin receptor agonists may be used.

(11) Because of the effect of angiotensin II agonists on the circulatory system, it is often useful to consider several factors when prescribing or administering an angiotensin II agonist. Such factors include: Concomitant therapy with angiotensin receptor blocking drugs Any known (history or presence of any) aortic or peripheral arterial aneurysm Congestive heart failure, myocardial infarction, or cerebrovascular infarct or hemorrhage within the previous 3 months Symptomatic cardiac arrhythmias or angina pectoris Termination of a treadmill test for reasons other than claudication (eg, arthritis, lung disease, exercise-limiting cardiac disease, or skin or foot lesions that limit walking) Uncontrolled hypertension; supine arterial systolic BP>140 mmHg or diastolic BP>100 mmHg at screening Current treatment with anticoagulants (e.g. heparin or heparin-like compounds, warfarin) Known bleeding disorder Platelet count<50,000, bilirubin or AST or ALT>2 the upper limit of normal Pregnancy, lactation or plans to become pregnant during the course of treatment Morbid obesity, such as a body mass index greater than 40
Manufacture, Formulation, and Administration of Therapeutic Agents

(12) The methods of manufacturing angiotensin II agonists vary depending on the agonist to be used. For example, the methods for manufacturing peptides such as angiotensin II itself are well known in the art of synthetic organic chemistry and biotechnology.

(13) In one embodiment, glass vials containing 50 g angiotensin II (AII) packaged under inert gas (for example, supplied by Bachem) are used, along with pumps for administering AII infusions. AII is reconstituted in 5% D/W and added to a 250 mL glass bottle of 5% D/W to give a final concentration of Dose x Patient Weight (in kg) per mL, where Dose initially is 1 ng/kg or 2 ng/kg, but may subsequently be between 1 and 5 ng/kg or 1 and 10 ng/kg (for example, 3, 5, or 10 ng/kg), as specified by the protocol. The infusion pump delivers infusions at a rate of 0.5 mL/min or 1 mL/min but may be altered to deliver less than 0.5 mL/min or as much as 2 mL/min, as needed. The infusion rate may be lowered to 0.5 mL/min should systolic pressure rise more than 15 mm Hg. It may be preferred to use infusion pumps that are accurate at lower infusion rates, in which case the dissolved Dose would be correspondingly increased.

EXAMPLE

(14) The following example is provided for the purpose of illustrating the invention and should not be construed as limiting.

(15) Example 1

(16) Treatment of a Patient with an Angiotensin II Agonist During Hemodialysis

(17) A typical hemodialysis patient at risk for dialysis-associated cramping is treated as follows. The patient is administered a 1 ng/kg.Math.min angiotensin II infusion through the venous port of their hemodialysis line. Blood pressure is monitored before hemodialysis and during the infusion at 15-minute intervals. The infusion rate is increased to 2 ng/kg.Math.min if systolic blood pressure has not increased by more than 10 mm Hg above pre-dialysis levels. The infusion rate is increased in increments of 1 ng/kg.Math.min every 15 minutes to a maximum infusion rate of 5 ng/kg.Math.min if the increase in systolic pressure remains less than 10 mm Hg above pre-dialysis levels and the infusion rate is well tolerated by the patient. At any point the infusion rate is decreased by an increment of 1 ng/kg.Math.min if systolic pressure rises more than 10 mm Hg or is increased by an increment of 1 ng/kg.Math.min if systolic pressure falls more than 10 mm Hg below pre-dialysis levels. The infusion is tapered in decrements of 1 ng/kg.Math.min or discontinued if an increase of the systolic pressure is greater than 15 mm Hg or the patient reports headaches or other symptoms attributable to excess angiotensin II. The infusion rate is again increased by increments of 1 ng/kg.Math.min to a maximum infusion rate of 5 ng/kg.Math.min every 15 minutes if systolic pressure falls below its pre-dialysis levels. Tolerability of the final selected infusion rate is confirmed during the next hemodialysis session. Blood is optionally obtained just before the conclusion of such a dialysis session for measurement of AII plasma concentrations and estimation of AII elimination clearance.

Other Embodiments

(18) While the present invention has been described with reference to what are presently considered to be the preferred examples, it is to be understood that the invention is not limited to the disclosed examples. To the contrary, the invention is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.

(19) All publications, patents, and patent applications are herein incorporated by reference in their entirety to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety. Where a term in the present application is found to be defined differently in a document incorporated herein by reference, the definition provided herein is to serve as the definition for the term.

(20) Other embodiments are in the claims.