US 5,037,848 AGrant
Aryl-Cycloalkyl-Alkanolamines for Treatment of Epilepsy
Issue Date:1991-08-06
•2 Claims
Abstract
A compound and method are disclosed for reducing the effects of epilepsy, especially temporal lobe epilepsy. The treatment disclosed by the subject invention is provided by administering an aryl-cycloalkyl-alkanolamine substance having the general formula: ##STR1## The compounds procyclidine, biperiden, and trihexyphenidyl fall within this class of compounds. Although not previously recognized to be effective against epilepsy, all three representative compounds were tested against soman and pilocarpine, two cholinergic neurotoxins used in animal research on epilepsy. All three of those compounds were shown to be highly effective in providing protection against the seizures and neurological damage caused by cholinergic neurotoxins, even when administered only after the onset of convulsions.
Metadata
Assignee
- Washington University
Inventor
- John W. Olney
Application Information
Application Number:US 3987531
Filing Date:1989-08-25
Priority Date:1989-08-25
Art Unit:125
Classifications
IPC:
A61K 3140A61K 3155A61K 31445A61K 3116
Field of Search:
514400;408;212;319;428;625;630;653
Patent Drawings
This patent does not have any drawings.
Description
FIELD OF THE INVENTION
This invention is in the fields of pharmacology and neurology. It relates specifically to compounds and methods for preventing or suppressing epileptic seizures and for protecting against brain damage associated with severe epilepsy.
BACKGROUND OF THE INVENTION
A pattern of brain damage is often found at autopsy in individuals whose clinical history includes frequent episodes of prolonged epileptic seizures (Corsellis et al 1976; a list of complete citations is provided below). Such epilepsy-related brain damage occurs most frequently in association with a type of epilepsy known as temporal lobe epilepsy (also referred to as psychomotor epilepsy or complex partial seizures). In this type of epilepsy, episodes of seizure activity may be quite prolonged (i.e., they may last for several hours), and they are often very difficult to control with any drugs currently available. The mechanism by which prolonged seizures give rise to brain damage was unknown until recent animal studies provided evidence linking such damage to excitatory transmitter systems in the brain, primarily the glutamate transmitter system (Olney et al 1986).
It is impossible to demonstrate with certainty that any seizure or seizure-related brain damage in a non-human animal falls within the proper definition of "epilepsy." Therefore, seizures and brain damage in lab animals which appear to be comparable to human epilepsy are referred to as "epileptiform" rather than "epilepsy." In lab animals, epileptiform seizures and brain damage can be induced by convulsant drugs, as discussed below. They also occur spontaneously in some strains of lab animals which are specially bred to exhibit epileptiform symptoms. Despite limitations, animal models offer the only methods available to researchers for studying epilepsy, short of tests on humans. Therefore, researchers use animal models to test drugs for anti-convulsant potential, and a great deal of research has been devoted to identifying drugs which generate epileptiform manifestations (i.e., seizure activity) and consequences (particular types of brain damage) that most closely resemble the manifestations and consequences of epilepsy in humans.
Three of the convulsant drugs that are of interest to researchers studying epilepsy are (1) kainic acid, a glutamate agonist (Nadler 1981); (2) pilocarpine, a cholinergic agonist (Clifford et al 1987); and (3) soman, a cholinesterase inhibitor (McLeod et al 1984). In several important respects, both the manifestations and the consequences of severe cases of epilepsy, especially temporal lobe epilepsy, resemble the manifestations and consequences of each of those convulsant drugs. Each of those substances can cause continuous seizure activity which can persist for hours, similar to "status epilepticus" in humans. In addition, each of those substances causes disseminated brain damage which resembles the damage observed during autopsies of humans who suffered from severe epilepsy.
A number of efforts to treat lab animals against convulsions induced by kainic acid, pilocarpine, and soman have focused on tranquilizers and sedatives. Diazepam (sold under the trade name Valium) suppresses seizures induced by these agents, but only at relatively high doses which are overly sedating (Clifford et al 1982; Fuller et al 1981). This makes such agents undesirable, especially as a long-term preventive measure.
Braitman et al 1988 states that a substance referred to as MK-801 (a glutamate antagonist, discussed below) provides some degree of protection against soman, if administered before soman exposure and if used in conjunction with other protective agents. However, recent research by the inventor of the subject application has discovered that when MK-801, phencyclidine, or ketamine were used in an effort to protect lab animals against pilocarpine, the seizure activity was made worse and the outcome was rapidly lethal. Although the reasons for these apparently conflicting results are not entirely clear, both sets of results suggest that interactions between the cholinergic and glutamate receptor systems may be relevant to efforts to provide an effective method for protecting the brain against epileptic seizures and against brain damage which can result from such seizures. The following sections provide information on both the cholinergic and glutamate receptor systems.
Receptors, messenger molecules, agonists, and antagonists
The surfaces of nerve cells in the brain contain various types of receptor molecules. In general, a receptor molecule is a polypeptide which straddles a cell membrane. When a messenger molecule interacts with the exposed extracellular portion of the membrane receptor molecule, it triggers a difference in the electrochemical status of the intracellular portion of the receptor, which in turn provokes some response by the cell. The messenger molecule does not bond to the receptor; instead, it usually disengages from the receptor after a brief period and returns to the extracellular fluid. Most receptor molecules are named according to the messenger molecules which bind to them.
An "agonist" is any molecule, including the naturally occurring messenger molecule, which can temporarily bind to and activate a certain type of receptor. An agonist can cause the same effect as the natural messenger molecule, or in some cases it can cause a more intense effect (for example, if it has a tighter affinity for the receptor molecule and remains bound to the receptor for a prolonged period).
By contrast, an "antagonist" is a molecule which can block or reduce the effects exerted by the natural messenger molecule. This can happen in several different ways. A "competitive antagonist" binds to a certain type of receptor without triggering it, thereby preventing the natural messenger molecule from reaching and activating the receptor. A "non-competitive antagonist" functions in other ways. For example, a receptor referred to as the PCP receptor, which is triggered by molecules such as PCP or MK-801, apparently can override the effects of a different type of receptor, the NMDA receptor (both receptors are discussed below). Therefore, PCP and MK-801 are regarded as non-competitive antagonists for the NMDA receptor.
Whether a given molecule is classified as an agonist or antagonist depends on the receptor context. For example, while MK-801 is an antagonist for the NMDA receptor, it is an agonist for the PCP receptor. Most agonists and antagonists are xenobiotic drugs, i.e., they do not exist naturally in the body.
For more information on neurotransmitters, receptors in the brain and central nervous system, and agonists and antagonists which interact with brain cell receptors, see Adelman 1987.
The two classes of excitatory receptor molecules that are of interest with respect to the subject invention are referred to as "cholinergic" receptors and "glutamate" (also called "EAA") receptors, discussed below. Both types of receptors are present in the synaptic junctions that serve as pathways for impulses between nerve cells in the brain. They are believed to be the two main classes of excitatory receptors. Most other types of receptors in the brain involve inhibitory neurotransmitters.
Cholinergic receptors
Cholinergic receptors are activated by acetyl choline, a relatively small molecule released by certain types of brain cells. Cholinergic receptors are divided into two main classes: the muscarinic receptors (which are further subdivided into M1 and M2 receptors), and the nicotinic receptors.
After a molecule of acetyl choline performs its neurotransmitter function, it is quickly degraded by an enzyme called cholinesterase. Some types of toxins, including the nerve gas soman and some types of insecticides, generate toxic effects by inhibiting the cholinesterase enzyme. If that enzyme is disabled, an excess of acetyl choline accumulates in the extracellular fluid, where it causes uncontrolled firing of the nerve cells and results in severe neural damage, typically ending in death.
Pilocarpine acts in a different manner, as an agonist at cholinergic receptors. It can cause a severe syndrome consisting of continuous "clonic" seizure activity (seizure activity manifested by shaking; a "tonic" seizure is manifested by muscle rigidity) that often terminates in death. After an hour of such seizure activity, acute neuronal degeneration is evident (Clifford et al 1987). A high dose of pilocarpine (400 mg/kg subcutaneously) is usually required to cause this syndrome, and rats show considerable individual variability in sensitivity. However, it is possible to produce this cholinotoxic syndrome consistently with a low dose of pilocarpine (30 mg/kg) if it is preceded by a priming dose of lithium (Honchar et al 1983). Therefore, the lithium/pilocarpine syndrome has become a useful animal model for studying cholinergic neurotoxic mechanisms and seizure-related brain damage.
Glutamate receptors
Glutamic acid and aspartic acid are amino acids. Each contains two carboxylic acid groups. Either of those amino acids, and various analogs of those molecules, can trigger a class of receptors referred to as "excitatory amino acid" (EAA) receptors.
EAA receptors are also referred to as "glutamate" receptors, for several reasons. At the normal pH which exists in the brain, glutamic acid dissociates to form its ion, glutamate, which is naturally present in high concentrations inside the brain cells. Glutamate was the first molecule shown to trigger EAA receptors, and glutamate has been shown to trigger all three known subtypes of EAA receptors. It is suspected of being the natural transmitter at all EAA receptors.
There are three known types of glutamate receptors. One type is called the kainic acid (KA) receptor, since it can be triggered (in lab conditions) by kainic acid, a glutamate agonist which normally does not exist inside the brain. As mentioned above, kainic acid, a potent convulsant, is used in lab animals to study the mechanisms of epileptic seizures and epilepsy-related brain damage.
Another type of glutamate receptor is called the quisqualate (QUIS) receptor, since it can be triggered by quisqualic acid, another convulsant drug.
The third known type of glutamate receptor is called the NMDA receptor. The molecule N-methyl aspartate (NMA) is an analog of glutamate. Like all amino acids except glycine, it exists in two different isomers, the D and L forms. The D isomer of NMA--referred to as NMDA--exerts a powerful agonist effect on some glutamate receptors. Therefore, those receptors are referred to as NMDA receptors.
Each type of glutamate receptor controls a set of ion channel. For example, when an NMDA receptor is triggered by a glutamate molecule or a related agonist, it opens an ion channel which causes sodium and calcium to enter the cell while potassium is transported out of the cell.
Some molecules block the effects of glutamate on NMDA receptors, but they apparently do not act by directly blocking or occupying NMDA receptors; instead, they appear to activate other receptors (PCP receptors) which block the opening of the NMDA-receptor-controlled ion channels. In effect, they override the effects of the NMDA receptors, acting as "non-competitive antagonists." Such molecules include phencyclidine (PCP) and ketamine (see Anis et al 1983), and various phencyclidine derivatives (Berry et al 1983). Phencyclidine and ketamine reduce the excitatory effects of NMDA receptors, while they have no direct effect on the ion channels controlled by KA and QUIS receptors (Anis 1983).
The drug {(+)-5-methyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5,10-imine maleate)}, commonly referred to as MK-801, is also a non-competitive antagonist of the NMDA receptor site (Wong 1986). It is a highly competitive agonist for the PCP receptor.
PCP, ketamine, and MK-801 are of interest because they can cross the blood-brain barrier and reach brain cells. Other NMDA antagonists such as D-.alpha.-amino-5-phosphonopentanoate are also glutamate antagonists; however, since they cannot cross the blood-brain barrier, they are of little interest to neurologists.
Glutamate neurotoxicity
Glutamate normally exists at relatively high concentration (roughly 10 millimolar (mM)) inside axons. It is released by axon terminals very sparsely and in a very controlled manner, so that it directly enters a synaptic cleft and contacts a synaptic glutamate receptor. The only known mechanism for terminating the excitatory action of glutamate is to remove it from the synaptic cleft. This is normally achieved by energy-dependent transport systems that transport the extra-cellular glutamate back inside the axon terminals.
Certain types of low energy conditions can impair the ability of the glutamate transport system to control the amount of extracellular glutamate. Such conditions can include hypoglycemia (low blood sugar), ischemia (reduced blood flow, such as caused by stroke or heart attack), and hypoxia (low oxygen levels, caused by problems such as severe anemia, hemoglobin defects, carbon monoxide poisoning, and asphyxia). Under those conditions, brain cells release glutamate and, because of the energy deficiency, the transport systems are unable to move the glutamate back into the cells at an adequate rate. When present in abnormal concentrations in the extracellular fluid, glutamate is in continuous contact with and hyper-stimulates its receptors. This can cause "excitotoxic" degeneration of nerve cells bearing such receptors. "Excitotoxic" is a term referring to the specific type of excitatory neurotoxicity that glutamate or related EAA's possess (Olney et al 1983).
This problem can be severely aggravated by the fact that initial glutamate release can stimulate further release of glutamate, which results in a cascade of extracellular glutamate accumulation and neurotoxic injury. It is believed that some of the neurotoxic injury associated with hypoxia or ischemia involves the action of glutamate at NMDA receptors, since such injury can be reduced or prevented by administering NMDA antagonists such as PCP, ketamine, and MK-801 (Lawrence et al 1987; Olney et al 1989).
It is also believed that in either the pilocarpine or soman cholinotoxic syndromes, persistent seizure activity is triggered by the excitatory activation of muscarinic cholinergic receptors, but much of the brain damage which ensues may be caused by seizure-mediated release of excessive glutamate at NMDA receptors. However, when NMDA antagonists such as phencyclidine, MK-801 or ketamine, which protect the brain against damage associated with kainic acid-induced seizures (Labruyere et al 1986), were administered to lithium/pilocarpine-treated rats by the inventor of the subject invention, a reaction was seen in which the seizure activity was made worse and the outcome was rapidly lethal. This unexpected finding suggests that an unknown mechanism operates in which phencyclidine, ketamine, or MK-801 interact with the cholinergic transmitter system to potentiate cholinergic activity.
Another potential disadvantage of using PCP, ketamine, or MK-801 for protecting against seizure-related neuropathology is that phencyclidine, the prototypic compound in this class, induces psychotomimetic effects in humans (Goodman et al 1975). Moreover, the inventor of the subject invention has recently discovered that phencyclidine, MK-801 and ketamine induce a neurodegenerative reaction in the posterior cingulate and retrosplenial cerebral cortex when administered in relatively low doses to adult rats (Olney et al 1989).
Prior to this invention, there has been no effective way for protecting mammals (including humans) against cholinergic neurotoxins such as soman or pilocarpine. The subject invention provides the most effective and reliable method discovered to date for treating mammals against those convulsant drugs. Because the effects of these convulsants are similar to the effects of certain types of epilepsy, in terms of both seizure activity and histological brain damage, there is a strong indication that an agent which can provide useful and effective protection against soman and pilocarpine may also be capable of providing at least some degree of protection against at least some types of epilepsy which have previously been regarded as intractable.
Aryl-cycloalkyl-alkanolamine compounds
Several aryl-cycloalkyl-alkanolamine drugs, including procyclidine, biperiden, and trihexyphenidyl, are known to have anti-cholinergic actions and have been identified for treatment of Parkinson's disease. Such compounds ameliorate the muscle rigidity and akinesia associated with Parkinsonism and extrapyramidal symptoms associated with neuroleptic drug treatment (Goodman et al 1975).
Some of these compounds have also been shown to have some degree of NMDA receptor antagonist properties, in that they reduce NMDA-induced neuronal degeneration in isolated chick embryo retinas (Olney et al 1987). Although these agents apparently compete with phencyclidine receptor ligands for binding at the PCP receptor, they are quite weak in PCP receptor activity compared to phencyclidine receptor ligands such as phencyclidine itself and MK-801.
The compound .alpha.-cyclohexyl-.alpha.-phenyl-1-pyrrolidinepropanol, commonly known as procyclidine, is described in U.S. Pat. No. 2,891,890 (Adamson 1959) as an anti-Parkinsonian drug. It is marketed under the trade name Kemadrin by Burroughs-Wellcome.
The compound commonly known as biperiden, .alpha.-bicyclo[2.2.1]-hept-5-en-2-yl-.alpha.-phenyl-1-piperidine-propanol , has been studied for its mood altering effects (Fleischhacker et al 1987) and for its interaction with brain muscarinic cholinoceptors (Syvalahti et al 1987). The hydrochloride salt of biperiden has been studied for its interaction with nicotine and oxotremorine in rat diaphragm (Das et al 1977). Biperiden is marketed under the trade name "Akineton" by Knoll.
The compound .alpha.-phenyl-.alpha.-tricyclo[2.2.1.02,6]-hept-3-yl-1-piperidinepropanol , commonly known as triperiden, is an anti-Parkinsonism agent which also reportedly has anti-viral properties (Schroeder et al 1985). It is marketed in Europe under the trade name "Norakin" by VEB Fahlberg-List (Magdeburg, West Germany).
The compound .alpha.-cyclohexyl-.alpha.-phenyl-1-piperidinepropanol, commonly known as trihexyphenidyl, is a known anti-Parkinsonian which has been studied for its effects in schizophrenic patients (Hitri et al 1987) and for its effects on memory in elderly patients McEvoy et al 1987). It is marketed under the trade name "Artane" by Lederle.
Various other aryl-cycloalkyl-alkanolamine compounds have also been studied for varying purposes. For example, U.S. Pat. No. 4,031,245 mentions the compound .alpha.-cyclopropyl-.alpha.-[3-(trifluoromethyl)phenyl]-1-piperidinepropan ol and its hydrochloride derivative in a description of alkenyl and alkanylamines for treating depression. U.S. Pat. No. 3,553,225 mentions the compound .alpha.-phenyl-.alpha.-tricyclo[3.3.1.13,7]-dec-1-yl-1-piperidine-butanol in a description of adamantane derivatives as tranquilizers West German Offen. No. 1, 951,614, in a description of benzyl alcohol derivatives having sedative and ulcer-preventing properties, mentions the compounds .alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-cyclohexyl-1-piperidinebutanol , .alpha.-(4-amino-3-chlorophenyl)-.alpha.-cyclo-hexylhexahydro-1H-azepine- 1-butanol, .alpha.-(4-amino-3,5-dichlorophenyl)-.alpha.-cyclohexahydro-1H-azepine-1-b utanol, and .alpha.-(4-amino-3,5-dibromopheny .alpha.-cyclohexyl-1,8,8-trimethyl-3-azabicyclo[3,2,1]octane-3-butanol. The compound .alpha.-[1,1'-biphenyl]-4-yl-.alpha.-cyclohexyl-1-piperidine propanol hydrochloride was mentioned in a study of the potential analgetic activity of some reduced biphenyl Mannich bases (Mann et al 1976).
It has not been proposed that any of these drugs could or should be useful either in animals or humans as a treatment to prevent epileptic seizures or seizure-related brain damage. Prior to this invention, there has been no adequate method or pharmacological agent for preventing or controlling seizures caused by temporal lobe epilepsy, or for minimizing brain damage suffered from such seizures.
SUMMARY OF THE INVENTION
A compound and method are disclosed for reducing the effects of epilepsy, especially temporal lobe epilepsy. The treatment disclosed by the subject invention is provided by administering an aryl-cycloalkyl-alkanolamine substance having the general formula: ##STR2##
The compounds procyclidine, biperiden, and trihexyphenidyl fall within this class of compounds. Although not previously recognized to be effective against epilepsy, all three representative compounds were tested against soman and pilocarpine, two cholinergic neurotoxins used in animal research on epilepsy. All three of those compounds were shown to be highly effective in providing protection against the seizures and neurological damage caused by cholinergic neurotoxins, even when administered only after the onset of convulsions.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
This invention relates to a compound and method for reducing the effects of epilepsy. As used herein, the effects of epilepsy include (1) manifestations such as seizure activity, and/or (2) consequences such as neurological or brain damage, which are associated with one or more types of epilepsy.
The treatment disclosed by this invention can be provided by administering to a susceptible mammal an aryl-cycloalkylalkanolamine represented by Formula I: ##STR3## wherein R.sup.1 is one or more groups independently selected from hydrido, halo, alkyl, acyl, hydroxyalkyl, haloalkyl, aminoalkyl, alkoxy, amino, alkylamino and acylamino; wherein R.sup.2 is selected from hydrido, cycloalkyl, cycloalkenyl, halocycloalkyl, alkylcycloalkyl, acylcycloalkyl, hydroxycycloalkyl, haloalkylcycloalkyl, aminoalkylcycloalkyl, alkoxycycloalkyl, aminocycloalkyl, bicycloalkyl, bicycloalkenyl and tricycloalkyl wherein the bicycloalkyl, bicycloalkenyl and tricycloalkyl groups may be substituted with one or more groups selected from alkyl, halo, acyl, hydroxy, hydroxyalkyl, haloalkyl, acyl, alkoxy, amino and alkylamino; wherein each of R.sup.3 and R.sup.4 is independently selected from hydrido, alkyl, acyl, alkenyl, cycloalkyl, phenylalkyl, phenyl, aminoalkyl and alkylaminoalkyl; and wherein R.sup.3 and R.sup.4 may be taken together to form a cyclic group including the nitrogen atom of Formula I, and n is an integer selected from one through five.
Several compounds covered by Formula I are commercially available, including:
.alpha.-cyclohexyl-.alpha.-phenyl-1-pyrrolidinepropanol (common name "procyclidine"), which has the following structure: ##STR4##
.alpha.-cyclohexyl-.alpha.-phenyl-1-piperidinepropanol (common name "trihexyphenidyl"), which has the following structure: ##STR5##
.alpha.-bicyclo[2.2.1]hept-5-en-2-yl-.alpha.-phenyl-1-piperidinepropanol (common name "biperiden"), which has the following structure: ##STR6##
.alpha.-phenyl-.alpha.-tircyclo [2.2.1.02,6]hept-3-yl-1-piperidinepropanol (common name "triperiden") which has the following structure: ##STR7##
The following compounds also have chemical structures within the parameters described in Formula I:
3,3,5-trimethyl-.alpha.-phenyl-.alpha.-[2-(1-piperidinyl)ethylcyclohexaneme thanol;
4-hydroxy-.alpha.-4-diphenyl-.alpha.-tricyclo[2.2.1.02,6]hept-1-yl-1-piperi dinepropanol;
.alpha.-cyclopropyl-.alpha.-[3-(trifluoromethyl)phenyl]-1-piperidinepropano l
.alpha.-phenyl-.alpha.-tricyclo[3.3.1.13,7]dec-1-yl-1-piperidinebutanol;
.alpha.-phenyl-.alpha.-tricyclo[2.2.1.02,6]hept-3-yl-1-piperidinepropanol
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-cyclohexyl-1-piperidinebutanol;
.alpha.-(p-chlorophenyl)-.alpha.-cyclohexyl-1-piperidinepropanol
.alpha.-(4-amino-3-chlorophenyl)-.alpha.-cyclohexylhexahydro-1H-azepine-1-b utanol;
.alpha.-cyclohexyl-.alpha.-(p-methoxyphenyl)-1-piperidinepropanol;
.alpha.-(4-amino-3,5-dichlorophenyl)-.alpha.-cyclohexylhexahydro-1H-azepine -1-butanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-cyclohexyl-1,8,8-trimethyl-3-az abicyclo[3.2.1]octane -3-butanol;
.alpha.-[1,1'-biphenyl]-4-yl-.alpha.-cyclohexyl-1-piperidine-propanol;
.alpha.-phenyl-.alpha.-tricyclo[3.3.1.13,7]dec-1-yl-1-pyrrolidinepropanol
.alpha.-(3,3-dimethylbicyclo[2.2.1]hept-2-yl)-.alpha.-phenyl-1-piperidinepr opanol;
.alpha.-cyclohexyl-4-hydroxy-.alpha.-4-diphenyl-1-piperidinepropanol
.alpha.-cyclopropyl-.alpha.-[3-(trifluoromethyl)phenyl]-1-piperidinepropano l;
.alpha.-cyclohexyl-.alpha.-phenyl-3-azabicyclo[3.2.2]nonane-3-propanol
.alpha.-[2-(diethylamino)ethyl]-.alpha.-phenylcyclohexanemethanol;
.alpha.-cyclopentyl-.alpha.-(3-(dimethylaminopropyl]-p-methoxybenzyl alcohol;
.alpha.-[3-(dimethylamino)propyl]-.alpha.-(.alpha.,.alpha.,.alpha.-trifluor o-m-tolyl)-cyclohexanemethanol;
.alpha.-[3-(dimethylamino)propyl]-.alpha.-m-tolylcyclohexanemethanol;
.alpha.-(p-bromophenyl)-.alpha.-[3-(dimethylamino)propyl]cyclohexanemethano l;
.alpha.-(p-chlorophenyl)-.alpha.-[3-(dimethylamino)propyl]cyclohexanemethan ol;
m-chloro-.alpha.-cyclopentyl-.alpha.-[3-(dimethylamino)propyl]benzyl alcohol;
.alpha.-cyclopentyl-.alpha.-[3-(dimethylamino)propyl]benzyl alcohol;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-methoxyphenyl)cyclohexanemethan ol
.alpha.-[2-(diethylamino)ethyl]-.alpha.-(p-methoxyphenyl)cyclohexanemethano l;
.alpha.-(p-chlorophenyl)-.alpha.-[2-(dimethylamino)ethyl]cyclohexanemethano l;
.alpha.-(p-chlorophenyl)-.alpha.-[2-(diethylamino)ethyl]cyclohexanemethanol ;
.alpha.-(p-bromophenyl)-.alpha.-[2-(dimethylamino)ethyl]cyclohexanemethanol
.alpha.-(p-bromophenyl)-.alpha.-[2-(diethylamino)ethyl]cyclohexanemethanol
.alpha.-[2-(diethylamino)ethyl]-o-phenylcyclohexanemethanol
.alpha.-(3-dimethylaminopropyl)-.alpha.-phenylcyclohexanemethanol
.alpha.-(2-dimethylaminoethyl)-.alpha.-phenyl-1-cyclohexene-1-methanol;
.alpha.-[5-[(2-diethylaminoethyl)methylaminolpentyl]-.alpha.-phenylcyclohex anemethanol;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-propoxyphenyl)cyclohexanemethan ol;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-methoxyphenyl)cyclohexanemethan ol;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-ethoxyphenyl)cyclohexanemethano l;
.alpha.8 2-(dimethylamino)ethyl]-.alpha.-(p-isopropoxyphenyl)cyclohexanemethanol;
.alpha.-(p-butoxyphenyl)-.alpha.-[2-(dimethylamino)ethyl]cyclohexanemethano l;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-isobutoxyphenyl)cyclohexanemeth anol;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-isopentyloxy)phenylcyclohexanem ethanol;
.alpha.-[2-(dimethylamino)ethyl]-.alpha.-(p-pentyloxy)phenyl]cyclohexanemet hanol;
.alpha.-(4-amino-3-bromophenyl)-.alpha.-[3-diethylamino)propyl]cyclohexanem ethanol;
.alpha.-(4-amino-3-chlorophenyl)-.alpha.-[3-diethylamino)propyl]cyclohexane methanol;
.alpha.-(4-amino-3,5-dichlorophenyl)-.alpha.-[3-dimethylamino)propyl]cycloh exanemethanol;
.alpha.-(4-amino-3,5-dichlorophenyl)-.alpha.-[3-diethylamino)propyl]cyclohe xanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-dimethylamino)propyl]cyclohe xanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(ethylmethylamino)propylcycl ohexanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(diethylamino)propyl]-cycloh exanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(dipropylamino)propylcyclohe xanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(diallylamino)propylcyclohex anemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(dibutylamino)propylcyclohex anemethanol;
.alpha.-['4-amino-3,5-dibromophenyl)-.alpha.-[3-(cyclohexylmethylamino)prop yl]cyclohexanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(benzylmethylamino)propyl]cy clohexanemethanol;
.alpha.-(4-amino-3,5-dibromophenyl)-.alpha.-[3-(N-methylanilino)propyl]cycl ohexanemethanol;
N-[2,6-dichloro-4-[1-cyclohexyl-4-(diethylamino)-1-hydroxybutyl]phenyl]acet amide;
.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]benzenemethanol;
.alpha.-cyclopropyl-.alpha.-[3-(dimethylamino)propyl]benzenemethanol;
.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]-4-methoxybenzenemethan ol
.alpha.-cyclopropyl-.alpha.-(2-(dimethylamino)ethyl]-3-(trifluoromethyl)ben zenemethanol
.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]benzenemethanol;
.alpha.-cyclopropyl-.alpha.-[3-(dimethylamino)propyl]benzenemethanol;
.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]-4-methoxybenzenemethan ol;
.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ehtyl]-3-(trifluoromethyl)-be nzenemethanol;
N-[3-cyclopropyl-3-hydroxy-3-[3-(trifluoromethyl)phenyl]propyl-N-methylacet amide;
3-chloro-.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]benzenemethano l
.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]-4-(trifluoromethyl)ben zenemethanol
.alpha.-cyclopropyl-.alpha.-[2-(diethylamino)ethyl]-3-(trifluoromethyl)benz enemethanol
.alpha.(dimethylamino)methyl]-.alpha.-(2-methylcyclopropyl)benzenemethanol;
.alpha.-cyclopropyl-.alpha.-2-(dimethylamino)ethyl]-4-(trifluoromethyl)benz enemethanol;
.alpha.-cyclopropyl-.alpha.-[2-(diethylamino)ethyl]-3-(trifluoromethyl)benz enemethanol;
3-chloro-.alpha.-cyclopropyl-.alpha.-[2-(dimethylamino)ethyl]benzenemethano l;
.alpha.-(2-diethylaminoethyl)-.alpha.-phenyl-5-norbornene-2-methanol;
.alpha.-(2-diethylaminoethyl)-.alpha.-phenyl-1-cyclohexene-1-methanol;
.alpha.-(3-dimethylaminopropyl)-.alpha.-phenyl-cyclohexanemethanol.
Any compound listed above may be tested by a routine screening process, as described in the Examples, to assess the effectiveness of that particular compound against cholinergic toxins used as laboratory models to simulate epilepsy.
The term "hydrido" denotes a single hydrogen atom (H) which may be attached, for example, to a carbon atom or to an oxygen atom to form an hydroxyl group. The term "alkyl" embraces linear or branched radicals having one to about ten carbon atoms. The term "cycloalkyl" embraces radicals having three to about ten carbon atoms, such as cyclopropyl and cyclobutyl. The term "haloalkyl" embraces radicals wherein one or more of the alkyl carbon atoms is substituted with one or more halo groups, preferably selected from bromo, chloro and fluoro. Dihaloalkyl and polyhaloalkyl groups may be substituted with two or more of the same halo groups, or may have a combination of different halo groups. The terms "alkylol" and "hydroxylalkyl" embrace linear or branched alkyl groups having one to ten carbon atoms, any one of which may be substituted with one or more hydroxyl groups. The term "alkenyl" embraces linear or branched radicals having two to about ten carbon atoms and containing at least one carbon-carbon double bond. The terms "alkoxy" and "alkoxyalkyl" embrace linear or branched oxy-containing radicals having alkyl portions of one to ten carbon atoms, such as methoxy group. The "alkoxy" or "alkoxyalkyl" radicals may be further substituted with one or more halo atoms, such as fluoro, chloro or bromo, to provide haloalkoxy or haloalkoxyalkyl groups. Examples of other substituents forming compounds of Formula I are as follows:
Alkenyl and alkynyl groups may have one unsaturated bond, such as an allyl group, or a plurality of unsaturated bonds, with such bonds adjacent, such as allene-type structures, in conjugation, or separated by several saturated carbons.
Included within the family of compounds of Formula I, are the tautomeric forms of the described compounds, isomeric forms including diastereomers, and the pharmaceutically-acceptable salts thereof.
The term "pharmaceutically-acceptable salts" embraces salts commonly used to form alkali metal salts and to form addition salts of free acids or free bases. Since the compounds of Formula I contain basio nitrogen atoms, such salts are typically acid addition salts. The nature of the salt is not critical, provided that it is pharmaceutically acceptable, and acids which may be employed to form such salts are well known to those skilled in this art. Examples of acids which may be employed to form pharmaceutically acceptable acid addition salts include such inorganic acids as hydrochloric acid, sulphuric acid and phosphoric acid, and organic acids such as maleic acid, succinic acid and citric acid. Other salts include salts with alkali metals or alkaline earth metals, such as sodium, potassium, calcium and magnesium. All of these salts may be prepared by conventional means from the corresponding compound of Formula I by reacting, for example, the appropriate acid with the compound of Formula I.
Methods of synthesis of representative compounds of Formula I are known. For example, synthesis of procyclidine and its salts are shown in U.S. Pat. No. 2,891,890 and U.S. Pat. No, 2,826,590. Synthesis of trihexyphenidyl hydrochloride is described in U.S. Pat. No. 2,682,543. Synthesis of biperiden is described in U.S. Pat. No. 2,789,110.
Administration of compounds within Formula I to humans can be by any technique capable of introducing the compounds into the bloodstream of a human patient, including oral administration, and by intravenous, intramuscular and subcutaneous injections. The active compound is usually administered in a pharmaceutically-acceptable formulation, although in some acute-care situations a compound of Formula I may be administered alone. Such formulations may comprise the active compound together with one or more pharmaceutically-acceptable carriers or diluents. Other therapeutic agents may also be present in the formulation. A pharmaceutically-acceptable carrier or diluent provides an appropriate vehicle for delivery of the active compound without introducing undesirable side effects. Delivery of the active compound in such formulations may be by various routes including oral, nasal, topical, buccal and sublingual, or by parenteral administration such as subcutaneous, intramuscular, intravenous and intradermal routes.
EXAMPLES
Example 1:
Pilocaroine assay using procyclidine as pre-treatment
Adult male Sprague Dawley rats (300-400 g) were treated with lithium chloride (3 meq/kg subcutaneous (sc)), to potentiate the pilocarpine effect and reduce individual variability among the rats. One day later the experimental group was treated with procyclidine (75 mg/kg intraperitoneal (ip)). The control group was treated with an equivalent volume of saline. Thirty minutes later, both groups received a single treatment with pilocarpine (30 mg/kg sc).
Rats were observed over a 4 hour period for behavioral signs of neurotoxicity, including preconvulsive signs such as facial grimacing, head nodding, eye blinking, wet dog shakes, or evidence of convulsions, including rearing on hind limbs with clonic movements of the head and forelimbs. After 4 hours, they were anesthetized and perfused through the left cardiac ventricle and ascending aorta with an aldehyde fixative solution for 15 minutes, then the brains were removed from the skull and processed for histopathological evaluation by methods previously described for light and electron microscopy (Olney 1971).
The results were as follows: all of the rats in the saline control group, i.e., rats that received lithium/pilocarpine but not procyclidine, displayed the full behavioral syndrome of preconvulsive and convulsive symptoms with persistent seizure activity being present for the majority of the 4 hour observation period. All of these rats in the saline control group (n=6) had severe brain damage affecting the cerebral cortex, hippocampus, amygdala, piriform cortex, thalamus, lateral septum and substantia nigra. None of the treated rats (lithium/pilocarpine and procyclidine) displayed either preconvulsive or convulsive signs, and none (n=6) sustained brain damage.
EXAMPLE 2
Pilocarpine assay using procyclidine as post-treatment
In a second experiment, all conditions were the same except that the procyclidine (75 mg/kg i.p.) or saline was not administered until 30 min after pilocarpine. All of the rats in the saline control group (n=6) exhibited a full behavioral syndrome, including persistent seizures and disseminated brain damage.
Most of the rats in the treatment group had begun to seize before procyclidine was administered, but all convulsive behavior disappeared within 10 minutes after procyclidine administration and all of these rats (n=6) escaped brain damage.
Prior research on receptor binding data had suggested that procyclidine interacts weakly with phencyclidine receptors (Olney et al 1987). In addition, recent research by the inventor of the subject application (Olney 1989) indicated that phencyclidine and MK-801 can cause vacuolar cytopathological changes in the posterior cingulate and retrosplenial cerebral cortices. The correlation of those findings suggests that procyclidine might also cause some degree of PCP-like toxicity. To evaluate that possibility, the affected brain regions were examined in the rats (n=12) from the treatment groups in both of the the experiments described above (i.e., rats that received procyclidine either before or after the pilocarpine). There was no evidence of the vacuolar cytopathology that occurs following phencyclidine or MK-801 treatment.
EXAMPLE 3
Soman assay using procyclidine as post-treatment
A major problem in studying the soman cholinotoxic syndrome is the marked individual variation in sensitivity of experimental animals. Some adult rats develop status epilepticus (persistent seizures) within 5-15 minutes after receiving a dose of soman in the range of 90-125 ug/kg (micrograms/kilogram) i.p. Those animals typically sustain severe brain damage and die within 1 to hours. However, other rats can tolerate much higher doses of soman without exhibiting seizures or brain damage and such animals survive treatment without any apparent untoward effects. Administering lithium chloride 24 hours prior to soman causes a moderate, but consistent, increase in the percentage of animals susceptible to soman neurotoxicity.
In a study to evaluate the possibility that procyclidine might protect against the neurotoxic effects of soman, adult male Sprague Dawley rats (350-425 g) were pretreated with lithium chloride (3 mg/kg sc) and 24 hrs later given soman (125 ug/kg sc) and observed for symptoms. Animals that began convulsing were treated immediately either with saline (control group) or a single dose (75 mg/kg i.p.) of procyclidine (treatment group). Animals that did not convulse received no further treatment.
All animals were anesthetized and killed 4 hours after soman treatment and their brains examined histologically by methods described above. Rats that did not seize (n=28) did not have any brain pathology. All rats that seized and received saline (n=8) had severe disseminated brain damage. Rats that seized and received procyclidine (n=2), stopped seizing within 5 to 15 minutes; all of these rats escaped brain damage.
In a separate experiment, atropine, which like procyclidine is classified as an anti-cholinergic drug, was substituted for procyclidine in the above protocol. At doses up to 100 mg/kg i.p., atropine conferred no protection against soman neurotoxicity.
EXAMPLE 4
Soman assay using selected susceptible rats
In an additional experiment, the neuroprotective properties of procyclidine were exploited to establish a colony of rats selectively bred for increased susceptibility to soman neurotoxicity. Adult male and female rats were challenged with soman. Those that responded with seizures (n=8) were identified as soman-sensitive and were treated with procyclidine which protected them, allowing them to survive and serve as breeding stock.
The first generation offspring of soman-sensitive male/female matings were challenged with soman and found to have a substantially increased rate of soman sensitivity (increased from 40% to 80%), even though lithium pretreatment was not used. Administration of procyclidine to these animals (n=8) when they started seizing, consistently caused cessation of seizures and protection against brain damage.
Thus, if experimental animals from the above studies are combined, the total number of rats protected against soman neurotoxicity by administration of procyclidine following onset of convulsive symptoms is 28. Although lithium pretreatment was employed in the first experiment, rats in the latter two experiments (n=16) received soman without lithium pretreatment. Therefore, either in the presence or absence of lithium, procyclidine provides effective protection against soman neurotoxocity.
EXAMPLE 5
Treatment with Biperiden or Trihexyohenidyl
Preliminary tests using a small number of rats were performed to determine whether biperiden or trihexyphenidyl were effective against a cholinergic neurotoxin. Rats were subjected to lithium priming and pilocarpine exposure as described in Example 2, and rats that showed seizure activity were treated with either biperiden or trihexyphenidyl. In all such rats, seizure activity ceased, and histological examination did not indicate any brain damage.
The positive results described above indicate that these compounds will be at least partially effective against temporal lobe epilepsy, and possibly against other forms of epilepsy as well.
Although this invention has been described with respect to specific embodiments, the details of these embodiments are not to be construed as limitations. Various equivalents and modifications may be made without departing from the spirit and scope of this invention, which is limited only by the claims which follow.
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Claims
What is claimed is:
1. A method for reducing the effects of temporal lobe epilepsy, which method comprises treating a mammal subject to seizure activity comparable to the symptoms of temporal lobe epilepsy with a therapeutically-effective amount of a compound of the formula: ##STR17## wherein R.sup.1 is one or more groups independently selected from hydrido, halo, alkyl, acyl, hydroxyalkyl, haloalkyl, aminoalkyl, alkoxy, amino, alkylamino and acylamino; wherein R.sup.2 is selected from hydrido, cycloalkyl, cycloalkenyl, halocycloalkyl, alkylcycloalkyl, acylcycloalkyl, hydroxycycloalkkyl, haloalkylcycloalkyl, aminoalkylcycloalkyl, alkoxycycloalkyl, aminocycloalkyl, bicycloalkyl, bicyclo-alkenyl and tricycloalkyl wherein the bicycloalkyl, bicycle-alkeny and tricycloalkyl groups may be substititued with one or more groups selected from alkyl, halo, acyl, hydroxy, hydroxyalkyl, haloalkyl, acyl, alkoxy, amino and alkylamino; wherein each of R.sup.3 and R.sup.4 is independently selected from hydrido, alkyl, acyl, alkenyl, cycloalkyl, phenylalkyl, phenyl, aminoalkyl and alkylaminoalkyl; and wherein R.sup.3 and R.sup.4 may be taken together to form a cyclic group including the nitrogen atom of Formula I, and n is an integer selected form one through five.
2. The method of claim 1, wherein said compound comprises an analog of .alpha.-cyclohexyl-.alpha.-phenyl-1-pyrrolidinepropanol (common name "propcyclidine") which is effective in reducing the effects of temporal lobe epilepsy.
Patent Citations (1)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US4945097 | 1990-07-01 | Olney |
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