Aminergic pharmaceutical compositions and methods
AssigneeBoard of Trustrees of Michigan State University
InventorsPatrick F. Dillon, Robert S. Root-Bernstein
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AssigneeBoard of Trustrees of Michigan State University
InventorsPatrick F. Dillon, Robert S. Root-Bernstein
Estimating the term…
Pharmaceutical compositions and method using aminergic compounds and complement compounds. Compositions are provided comprising: (a) a subefficacious amount of a non-adrenergic aminergic compound or of an adrenergic antagonist; and (b) a safe and effective amount of a complement compound. Methods are also provided comprising the administration of: (a) a low dose of a non-adrenergic aminergic compound or of any adrenergic antagonist; and (b) a safe and effective amount of a complement compound. Non-adrenergic aminergic compounds can comprise a histaminergic, dopaminergic, muscarinergic, serotoninergic, octopaminergic, or trace aminergic compound. Complement compounds include ascorbates, opioids, polycarboxylic acid chelators, resveratrols, cysteines, substituted derivatives and analogs thereof, and mixtures thereof. Preferred complements include ascorbates, particularly ascorbic acid. Methods include the treatment of: neurological and neural disorders; mood and behavior disorders; cardiac, vascular, and cardiovascular disorders; hypertension, headache; respiratory disorders; gastrointestinal disorders; obesity; asthma, allergy; smooth muscle contraction disorders; nasal or nasopharyngeal conditions; genitourinary disorders; ocular disorders, glaucoma; hormone- or neurotransmitter-release or -secretion disorders.
1-277. (canceled)
The pharmaceutical composition according to claim 277, wherein said complement is EDTA.
The pharmaceutical composition according to claim 274, wherein said complement comprises an opioid.
The pharmaceutical composition according to claim 274, wherein said complement comprises a resveratrol family member.
The pharmaceutical composition according to claim 274, wherein said complement comprises a cysteine family member.
The pharmaceutical composition according to claim 274, wherein said composition is suitable for oral administration.
The pharmaceutical composition according to claim 274, wherein said composition is suitable for topical administration.
The composition according to claim 273, wherein said non-adrenergic aminergic compound is a dopaminergic compound selected from the group consisting of quinpirole, carmoxirole, 2-amino-5,6-dihydroxy-1,2,3,4-tetrahydronaphthalene, lisuride, pergolide, apomorphine, haloperidol, domperidone, metaclopramide, spiperone, haloperidol, diphenylbutylpiperidine, ecopipam, fenoldopam, fluphenazine, flupentixol, sulpiride, phenothiazines, thioxanthenes, naloxone, bromocriptine, substituted dopamine derivatives;
The composition according to claim 273, wherein said non-adrenergic aminergic compound is a histaminergic compound selected from the group consisting of 2-(2-pyridyl)ethylamine, histaprodifen (2-[2-(3,3-diphenylpropyl)-1H-imidazol-4-yl]ethylamine), N-methyl-histaprodifen, N-alpha-2-[(1H-imidazol-4-yl)ethyl]histaprodifen, (6-[2-(4-imidazolyl)ethylamino]-N-(4-trifluoromethylphenyl)heptanecarboxamide), dexchlorpheniramine, diphenhydramine;
The composition according to claim 273, wherein said non-adrenergic aminergic compound is a muscarinergic compound, selected from the group consisting of aceclidine, arecoline, atropine, benzhexyl, benztropine, cevimeline, 2-ethyl-8-methyl-2,8-diazaspiro(4.5)decane-1,3-dione, R-(Z)-(+)-alpha-(methoxyimino)-1-azabicyclo[2.2.2]octane-3-acetonitrile, milameline, oxotremorine, pilocarpine, pirenzepine, scopolamine, talsaclidine, telenzepine, trihexyphenidyl, xanomeline, substituted acetylcholine derivatives;
The method according to claim 273, wherein said non-adrenergic aminergic compound is a serotoninergic compound, selected from the group consisting of amphetamines, ergotamine, lysergate derivatives, almotriptan, buspirone, chlorpromazine, clozapine, cisapride, cyanopindolol, cyproheptadine, dexfenfluramine, dextromethorphan, dolasetron, donitriptan, eletriptan, eltoprazine, fenfluramine, fluoxetine, fluvoxamine, gepirone, granisetron, ketanserin, loxapine, meperidine, mesulergine, methiothepin, metergoline, methysergide, metoclopramide, mianserin, naratriptan, 1-naphthylpiperazine, nefazodone, olanzapine, ondansetron, paroxetine, pindolol, propranolol, risperidone, ritanserin, rizatriptan, spiperone, sertraline, sumatriptan, tropisetron, zolmitriptan, 8-hydroxy-dipropylaminotetralin, 2-(2-methyl-4-chlorophenoxy)propanoic acid, substituted 5-hydroxy-tryptamine derivatives;
A pharmaceutical composition comprising:
A pharmaceutical composition comprising:
A method for treating a disorder associated with a non-adrenergic biogenic amine receptor in a human or animal subject, comprising:
A method for treating a disorder associated with a non-adrenergic biogenic amine receptor in a human or animal subject, comprising:
A method for determining a regimen for regulating a biogenic amine receptor in a human or animal subject, comprising:
A pharmaceutical composition comprising:
A pharmaceutical composition comprising:
A method for treating a disorder associated with an adrenergic receptor in a human or animal subject, comprising:
Dependencies are inferred from the claim text.