Claims
- 1. A method of eliciting in a mammal immediate cardiovascular responses similar to those cardiovascular responses elicited by aerobic activity comprising the administration of an exercise simulating agent with beta adrenergic activity which elicits immediate cardiovascular responses similar to those cardiovascular responses elicited by aerobic activity by closed loop drug delivery device.
- 2. A method of eliciting in a mammal adaptive cardiovascular and metabolic responses similar to the adaptive cardiovascular and metabolic responses elicited by aerobic activity comprising the administration of an exercise simulating agent with beta adrenergic activity which elicits adaptive cardiovascular and metabolic responses similar to the adaptive cardiovascular and metabolic responses elicited by aerobic activity to a mammal by means of closed loop transdermal iontophoretic infusion for 0.5 to 4.0 hours daily, for a period of from 1 to 30 days.
- 3. The method of claim 2 wherein said exercise simulating agent has the chemical formula: ##STR9## wherein X.sub.1 and X.sub.2 are independently hydrogen, hydroxy, methoxy or carbamoyl, provided that X.sub.1 and X.sub.2 are not both hydrogen or carbamoyl; one of Y.sub.1 and Y.sub.2 is hydrogen and the other is hydrogen or methyl, provided that if Y.sub.1 is methyl, then X.sub.1 is not carbamoyl; Z is hydrogen or hydroxy; and n is 2 or 3; or a pharmaceutically acceptable acid addition salt thereof.
- 4. The method of claim 3 wherein X.sub.1 is hydrogen, X.sub.2 is hydroxy, Y.sub.1 and Y.sub.2 are hydrogen, Z is hydroxy and n is 3.
- 5. The method of claim 3 wherein X.sub.1 is hydrogen, X.sub.2 is methoxy, Y.sub.1 and Y.sub.2 are hydrogen, Z is hydroxy and n is 2.
- 6. A method of eliciting in a mammal immediate cardiovascular responses similar to those cardiovascular responses elicited by aerobic exercise which comprises
- (a) administering an exercise simulating agent with beta adrenergic activity which elicits immediate cardiovascular responses similar to those cardiovascular responses elicited by aerobic exercise to said mammal by a closed loop drug delivery device;
- (b) controlling infusion of said exercise simulating agent into the bloodstream of said mammal so that a predetermined range of cardiovascular responses of said mammal is obtained;
- (c) monitoring the range of responses of said mammal; and
- (d) changing infusion of said exercise simulating agent as required to maintain said range of responses in said mammal.
- 7. A method of eliciting in a mammal immediate cardiovascular responses similar to those cardiovascular responses elicited by aerobic exercise which comprises
- (a) administering an exercise simulating agent with beta adrenergic activity which elicits immediate cardiovascular responses similar to those cardiovascular responses elicited by aerobic exercise to said mammal by a closed loop drug delivery device;
- (b) controlling infusion of said exercise simulating agent into the bloodstream of said mammal so that a predetermined range of cardiovascular responses of said mammal is obtained;
- (c) monitoring the range of responses of said mammal; and
- (d) changing infusion of said exercise simulating agent as required to maintain said range of responses in said mammal;
- wherein said exercise simulating agent comprises a compound of the formula:
- wherein X.sub.1 and X.sub.2 are independently hydrogen, hydroxy, methoxy or carbamoyl, provided that X.sub.1 and X.sub.2 are not both hydrogen or carbamoyl; one of Y.sub.1 and Y.sub.2 is hydrogen and the other is hydrogen or methyl, provided that if Y.sub.1 is methyl, then X.sub.1 is not carbamoyl; Z is hydrogen or hydroxy; and n is 2 or 3; or a pharmaceutically acceptable acid addition salt thereof.
- 8. The method of claim 7 wherein said predetermined level of response comprises reversible myocardial ischemia when coronary artery disease is present.
- 9. The method of claim 8 wherein said closed loop drug delivery device comprises an intravenous drug delivery device.
- 10. The method of claim 8 wherein said closed loop drug delivery device comprises a transdermal iontophoretic device.
- 11. The method of claim 8 wherein said exercise simulating agent is a compound wherein Z is hydroxy.
- 12. The method of claim 11 wherein said exercise simulating agent is a compound wherein X.sub.1 is hydrogen, X.sub.2 is hydroxy, Y.sub.1 and Y.sub.2 are both hydrogen and n is 3.
- 13. The method of claim 11 wherein said exercise simulating agent is a compound wherein X.sub.1 is hydrogen, X.sub.2 is methoxy, Y.sub.1 and Y.sub.2 are hydrogen and n is 2.
- 14. A method for increasing cardiac contractility in a mammal having depressed cardiac contractility which comprises administering to said mammal an effective amount of a compound of the formula: ##STR10## wherein X.sub.1 and X.sub.2 are independently hydrogen, hydroxy, methoxy or carbamoyl, provided that X.sub.1 and X.sub.2 are not both hydrogen or carbamoyl; one of Y.sub.1 and Y.sub.2 is hydrogen and the other is hydrogen or methyl, provided that if Y.sub.1 is methyl, then X.sub.1 is not carbamoyl; and n is 2 or 3; or a pharmaceutically acceptable addition salt thereof.
- 15. The method according to claim 14 wherein X.sub.1 is hydrogen, X.sub.2 is carbamoyl, Y.sub.1 is methyl, Y.sub.2 is hydrogen and n is 2.
- 16. A method for causing adaptive effects in a mammal which are similar to adaptive responses of said mammal (caused by aerobic exercise over a period of time which comprises administering to said mammal an effective amount of a compound of the formula: ##STR11## wherein X.sub.1 and Y.sub.2 are independently hydrogen, hydroxy, methoxy or carbamoyl, provided that X.sub.1 and X.sub.2 are not both hydrogen or carbamoyl; one of Y.sub.1 and Y.sub.2 is hydrogen and the other is hydrogen or methyl, provided that if Y.sub.1 is methyl, then X.sub.1 is not carbamoyl; and n is 2 or 3; or a pharmaceutically acceptable acid addition salt thereof.
- 17. The method of claim 16 wherein X.sub.1 is hydrogen, X.sub.2 is hydroxy, Y.sub.1 and Y.sub.2 are hydrogen and n is 3.
- 18. The method of claim 16 wherein X.sub.1 is hydrogen, X.sub.2 is methoxy, Y.sub.1 and Y.sub.2 are hydrogen and n is 2.
- 19. The method of claim 16 wherein X.sub.1 is hydrogen, X.sub.2 is carbamoyl, Y.sub.1 is methyl, Y.sub.2 is hydrogen and n is 2.
CROSS REFERENCE TO RELATED APPLICATIONS
This is a divisional of co-pending application Ser. No. 07/308,683 filed on Feb. 9, 1989 U.S. Pat. No. 5,108,363 which is a continuation-in-part of U.S. Ser. No. 157,875, filed Feb. 19, 1988 ABN., the disclosure of which is incorporated herein by reference.
US Referenced Citations (9)
Non-Patent Literature Citations (4)
Entry |
Frucht et al., "Computer-Assisted Control of Blood Pressure by Cardiovascular Drugs:Problems in Developing a Closed-Loop Control System" Aniasth. In.21:331-337 1986. |
Combs et al., "Evaluation of isoproterenol as a method of stress testing." Am. Hear J., 87:711-715 (1974). |
Wexler et al., "Electrocardiographic effects of isoprenaline in normal subjects and patients with coronary atherosclerosis." Br. Heart J., 33:759-764 (1971). |
Manca et al., "Comparison of Five Different Stress Testing Methods in the ECG Diagnosis of Coronary Artery Disease: Correlation with Coronary Arteriography." Cardio, 64:325-332 (1979). |
Divisions (1)
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Number |
Date |
Country |
Parent |
308683 |
Feb 1989 |
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Continuation in Parts (1)
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Number |
Date |
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157875 |
Feb 1988 |
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