US2001016582A1PendingUtilityA1

Method and composition for the treatment of lipid and glucose metabolism disorders

Priority: Apr 28, 1997Filed: Apr 28, 1997Published: Aug 23, 2001
Est. expiryApr 28, 2017(expired)· nominal 20-yr term from priority
A61K 31/55A61K 31/58
31
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Claims

Abstract

Disclosed are methods for modifying or regulating at least one of glucose or lipid metabolism disorders which comprises administering to a human or vertebrate subject a D 1 dopamine agonist in conjunction with a dopamine D 2 agonist where the conjoined administration is effective to improve at least one of the following lipid and glucose metabolic indices: body weight, body fat, plasma insulin, plasma glucose and plasma lipid, and plasma lipoprotein. In preferred embodiments, the administration of the D 1 dopamine agonist and the D 2 dopamine agonist is conducted at a predetermined time.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A method for modifying or regulating at least one of glucose or lipid metabolism disorders which comprises administering to a human or vertebrate animal subject in need of such modification or regulation a D 1  dopamine agonist in conjunction with a dopamine D 2  agonist wherein the conjoined administration is effective to improve at least one of the following lipid and glucose metabolic indices: body weight, body fat, plasma insulin, plasma glucose and plasma lipid, and plasma lipoprotein.  
     
     
         2 . The method of    claim 1    wherein the D 2  agonist is an ergot alkaloid is selected from the group consisting of 2-bromo-alpha-ergocriptive, 6-methyl 8 beta-carbobenzyloxyaminoethyl-10-alpha-ergoline, 8-acylaminoergoline, pergolide, lisuride, 6-methyl-8-alpha-(N-acyl) amino-9-ergoline, 6-methyl-8-alpha-(N-phenyl-acetyl)amino-9-ergoline, ergocomine, 9,10-dihydroergocomine, and D-2-halo-4-alkyl-8-substituted ergolines, D-2-bromo-6-methyl-8-cyanomethylergoline.  
     
     
         3 . The method of    claim 1    wherein the D 1  agonist comprises SKF38393.  
     
     
         4 . The method of    claim 2    wherein the ergot alkaloid comprises bromocriptine.  
     
     
         5 . The method of    claim 1    wherein the D 2  agonist is administered at a predetermined time of day.  
     
     
         6 . The method of    claim 5    wherein the D 1  agonist is administered at about the same time as the D 2  agonist.  
     
     
         7 . A method for modifying or regulating at least one of glucose or lipid metabolism disorders which comprises administering to a human or vertebrate animal subject in need of such modification or regulation a D 1  agonist in conjunction with at least one member selected from the group consisting of an adrenergic α 1  antagonist, an adrenergic α 2  agonist and a serotonergic inhibitor wherein the amount of the combination is sufficient to effect at least one of the following lipid and glucose metabolic indices: body weight, body fat, circulating insulin, plasma or blood glucose, plasma lipid and plasma lipoprotein.  
     
     
         8 . The method of    claim 7    wherein the D 1  agonist and the member of said group is administered at a predetermined time of day.  
     
     
         9 . The method of    claim 8    wherein the D 1  agonist is administered at about the same time as member of said group.  
     
     
         10 . A method for modifying or regulating at least one of glucose or lipid metabolism disorders which comprises administering to a human or vertebrate animal subject in need of said modification or regulation a D 1  agonist in conjunction with at least one of a α 2  agonist, a α 1  antagonist and a serotonergic inhibitor, and further in conjunction with a D 2  agonist sufficient to improve at least one of the following lipid and glucose metabolic indices: body weight, body fat, plasma insulin, plasma glucose and plasma lipid.  
     
     
         11 . A therapeutic agent combination for modifying or regulating at least one of glucose and lipid metabolism disorders comprising: 
 a first amount of a dopamine D 1  agonist; and    a second amount of at least one member selected from the group consisting of: 
 (i) a dopamine D 2  agonist; and  
 (ii) at least one of an adrenergic α 1  antagonist, an adrenergic α 2  agonist and a serotonergic inhibitor.  
   
     
     
         12 . A method for modifying or regulating at least one of glucose or lipid metabolism disorders comprising: 
 administering to a subject in need of said modification or regulation: 
 (i) a D 2  agonist in a first amount; and  
 (ii) at least one of an adrenergic α 1  antagonist, an adrenergic α 2  agonist and a serotonergic inhibitor in a second amount;  
 said first and second amounts being sufficient to improve at least one of the following indices of glucose or lipid metabolism: body weight, body fat, plasma insulin, plasma glucose and plasma lipid.

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