WO1995025509A2

WO1995025509A2 - Use of n-acyl derivatives of aminoalcohols in the manufacture of a medicament for practising neuroprotective action in neuropathological states connected with excitotoxicity

Info

Publication number: WO1995025509A2
Application number: PCT/EP1995/001002
Authority: WO
Inventors: Francesco Della Valle; Alberta Leon; Silvana Lorenzi
Original assignee: LifeGroup SpA
Current assignee: LifeGroup SpA
Priority date: 1994-03-21
Filing date: 1995-03-17
Publication date: 1995-09-28
Anticipated expiration: 1996-09-21
Also published as: AU2109095A; JPH09510467A; ITMI940523A1; US5925678A; WO1995025509A3; EP0804179B1; ATE182075T1; ITMI940523A0; EP0804179A2; DE69510825D1; IT1271623B

Abstract

The following description concerns the use of N-acyl derivatives of aminoalcohols with mono and dicarboxylic acids for the prevention and treatment of diseases connected with hyper and prolonged excitation by excitatory amino acids.

Description

USE OFN-ACYL DERIVATIVES OFAMINOALCOHOLS IN THE MANUFACTURE OF A MEDICAMENT FOR PRACTISING NEUROPROTECTIVE ACTION IN NEUROPATHOLOGICAL STATES CONNECTED WITH EXCITOTOXICITY

FIELD OF THE INVENTION

The present invention relates to the use of N-acyl derivatives of aminoalcohols with mono and dicarboxylic acids for the prevention and treatment of neuropathological states connected with excitotoxicity. PRIOR ART DISCLOSURE

Recent research has established that the nervous system is not an isolated entity but a component of a complex intercommunication system together with the main homeostatic systems - immune system and endocrine system - where stimuli from one of the three systems are received and adaptive responses are processed by the other two in order to maintain or regulate homeostatic equilibrium in the body. In fact, although the nervous system, the endocrine system and the immune system utilize languages of their own, they can translate and process the messages received from the other systems.

Scientific literature has recently reported some results suggesting that the mast cell, an immunocompetent cell ubiquitously present in tissues, might be the element providing communication between the three systems: due to the anatomic dislocation - in proximity of nerve endings and in contiguity with the vascular system - and to its functional role being evidenced, said cell might be capable of acting as a "gate keeper" within said complex system.

Following tissue injury, stimuli capable of activating mast cells are produced leading to the prompt release from preformed stores of mediators and other substances with chemotactic, proinflammatory and cytotoxic effects. Cytokines (TNF-α and interleukins), vasoactive amines (serotonin, bradikin and histamine), heparin and PAF are some examples. The presence of mediators and kinins at the site of injury increases the sensitivity to pain in the acute stage; further, the accumulation of IL-1, IL-3 and TNF-α induces the synthesis of NGF which locally increases the proinflammatory agonist stimulus (mast cell and T-lymphocyte proliferation, mast cell degranulation), which is thus amplified and prolonged (U. Otten et al., 1989. "Nerve Growth Factor induces growth and differentiation of human lymphocytes", PNAS 86: 10059-10063; J.S. Marshall et al., 1989. "The role of mast cell degranulation product in mast cell hyperplasia", The J. of Immunology, 144: 1886-1892) bearing at the consequence to induce even modifications in the number of nerve endings and facilitate these inflammatory conditions to become chronic (R. Dubner and M.A. Ruda, 1992. "Activity-dependent neuronal plasticity following tissue injury and inflammation", TINS, 15, 3: 96-103).

These and further evidences for the susceptibility and rapidity of mast cell degranulation phenomena suggested the need for an inhibitory control. In addition to the corticosteroid-mediated pleiotropic control, already characterized, a local control system has been developed by the Applicant, said system being pharmacologically applicable with specific compounds structurally related to endogenous autacoids and chemically definable as N-acyl lipids. as disclosed in European patent applicationsNo. 92121862.4 published with No. 0 550 006 A3 and No. 92121864.0 published with No. 0 550 008 A2.

The experimental evidence obtained by the Applicant for these N-acyl lipids proved the presence of a local antagonist endogenous regulation mechanism, meant to control mast cell degranulation induced by neurogenic and immunogenic supramaximal stimuli (ALIA = Autacoid Local Inflammation Antagonism). Said discovery is of great pharmacological importance, making it possible to synthesize drugs, chemically definable as N-acyl derivatives of mono and polycarboxylic acid with aminoalcohols, which can act as autacoids with the ability to modulate mast cell activation associated to neuroimmunogenic inflammatory processes in autoimmune diesases and other pathological conditions (see the aforementioned patent applications).

SUMMARY OF THE INVENTION

The Applicant has surprisingly found that compounds belonging to the class of N-acyl derivatives of mono and dicarboxylic acids with aminoalcohols which can exert a protective action against the neurotoxicity induced by excitatory amino acids (EAA), such as glutamic acid (hereinafter referred to as Glu), in neuronal cultures, when incubated at the same time or after exposure to the excitotoxic stimulus. The kinetics of this effect makes said compounds of high applicative interest in acute and chronic disorders of the central nervous system. Therefore, the present invention is related to the use of said N-acyl derivatives and of more soluble and/or slow release derivatives thereof as active principles in the preparation of pharmaceutical compositions for the prevention and treatment of acute and chronic diseases of the central nervous system connected with EAA neurotoxicity.

The compounds according to the present invention are defined by the following formulas (I) and (II):

where

is the acyl radical of a linear or branched, saturated or unsaturated aliphatic monocarboxylic acid, containing 2 to 20 carbon atoms , optionally substituted in the aliphatic chain with one of more hydroxyl , aminic , ketonic , carboxyl , cycloalkyl , aryl , heterocyclic, aromatic , heteroaromatic , polycyclic groups ; or the acyl radical of an aromatic , heteroaromatic or heterocyclic monocarboxylic acid;

is the diacyl radical of a saturated or unsaturated aliphatic dicarboxylic acid, optionally substituted with an aminic, hydroxyl or ketonic group; or the diacyl radical of an aromatic, heterocyclic or heteroaromatic dicarboxylic acid;

R₂ and R₅ are alcoholic residues selected from a C₁ -C₂₀ linear or branched hydroxyalkyl, optionally substituted in the aliphatic chain with one or more aryl groups, and a hydroxyaryl optionally substituted with one or more linear or branched alkyl radicals of from 1 to 20 carbon atoms; in both cases, the hydroxyl group is optionally esterified to - 0X, wherein X is the acyl radical of a linear or branched, saturated or unsaturated, aliphatic acid, optionally substituted in the aliphatic chain with one or more aryl groups or with one -COOH optionally salified, or X is the acyl radical of an aromatic acid or -PO₃H₂ optionally salified;

R₃ is H or R₂;

R₆ is H or R₅.

DETAILED DESCRIPTION OF THE INVENTION

The characterization and advantages of N-acyl derivatives of mono and dicarboxylic acids of aminoalcohols as active compounds able to counteract the neuronal death induced by excitotoxic event and, therefore, useful for the treatment of diseases connected with a hyper and prolonged stimulation of EAA receptors will be described in detail hereinafter.

In the derivatives of formula (I), when is the acyl radical of a saturated or unsaturated aliphatic

monocarboxylic acid, it is preferably selected from the group consisting of acetic, caproic. butyric, palmitic, oleic, stearic, lauric, linoleic, linolenic and myristic acid and hydroxyl, aminic and ketonic homologues thereof, glycolic, pyruvic, lactic, caprylic, valeric, valproic, arachidonic acid, gamma-trimethyl-β-hydroxybutyrobetaine and derivatives thereof acylated on the hydroxyl group; when is the acyl radical of an aromatic , heteroaromatic or

heterocyclic monocarboxylic acid, it is preferably selected from the group consisting of salicylic , acetylsalicylic , benzoic , trimethoxybenzoic , isonicotinic , thenoic , phenylanthranilic , retinoic, hydroxyphenylaceric , α-lipoic ( thioctic) and deoxycholic acid. In the derivatives of formula (II) , when is the diacyl radical of a saturated or unsaturated

aliphatic dicarboxylic acid, it is preferably selected from the group consisting of oxalic, fumaric, azelaic, succinic, traumatic, glutaric and muconic acid and hydroxyl, aminic and ketonic homologs thereof, malic, aspartic and tartaric acid; when is the diacyl radical of an aromatic,

heteroaromatic or heterocyclic dicarboxylic acid, it is preferably selected from the group consisting of phthalic, folic and chromoglycic acid.

R₂, R₃, R₅, and R₆, are preferably radicals of aminoalcohols selected from the group consisting of monoethanolamine, diethanolamine, 2-hydroxypropylamine and di-(2-hydroxypropyl)-amine, wherein the hydroxyl group is optionally esterified to aliphatic esters, araliphatic esters, aromatic esters, 0-phosphates, acid hemiesters or salified derivatives thereof.

Therefore, with reference to formula (I), the compounds of the present invention have preferably the following structures:

p

o

where X is H, -PO₃H₂, optionally salified with monovalent or bivalent inorganic ions, or X is the acyl radical of a linear or branched, saturated or unsaturated, aliphatic carboxylic acid, optionally substituted on the aliphatic chain with one or more aryl groups or with one -COOH optionally salified with monovalent or bivalent inorganic ions, and is preferably , and ; or X is the acyl radical of

an aromatic carboxylic acid, preferably benzoic acid.

Said monovalent or bivalent inorganic ions are preferably K, Na, Mg or Ca.

With reference to formula (II), the compounds of the present invention have preferably the following structures:

where X is defined as above.

It is to be noted that chemical group X serves to increase the solubility in water and/or to modify the pharmacokinetic properties of the compound, giving a pro-drug.

It is also to be noted that the derivatives of the aminoalcohols 2-hydroxypropylamine and di-(2-hydroxypropyl)-amine can be racemic or optical isomers.

The compounds according to the present invention are prepared by the different methods described hereinbelow.

Method of synthesis A

High-temperature melting of alkanolamine salt with a carboxylic acid. with formation of the relevant alkanolamide.

Procedure:

a mixture consisting of a carboxylic acid and an alkanolamine (1:1.5 equivalents) is fed to a flask provided with reflux condenser and heated to 130-l60°C, for 4 to 8 hrs, on an oil bath. The alkanolamide obtained is purified by a method or by a combination of methods reported below:

- fractional distillation in vacuo;

- liquid/liquid extraction;

- crystallization from a suitable solvent or mixture of volatile solvents , selected from the classes of alcohols , ketones , esters , ethers , hydrocarbons or chlorinated solvents ;

- liquid chromatography using an ion exchange resin , silica gel or alumina as stationary phase, or a reversed phase adsorbent selected among those available on the market, consisting of polymers or silica.

Method of synthesis B

N-acylation of an alkanolamine with a suitable carboxylic acid activated derivative.

Procedure:

an alkanolamine solution in a suitable solvent or mixture of solvents, selected from the group consisting of water, alcohols, ketones, esters, ethers, chlorinated solvents, dialkylamides, dialkylsulphoxides and heterocycles, is cold stirred. The carboxylic acid activated derivative

(acyl halide, anhydride or alkylester) is added slowly over a period of

30 min to 3 hrs.

Acylation can be carried out in the presence of a suitable base, selected from the group consiting of hydroxides, inorganic carbonates and bicarbonates and organic tertiary amines, at a temperature ranging from - 20°C to +120°C. The alkanolamide obtained is purified by a method or by a combination of methods as per Method A.

Method of synthesis C

Activation of the carboxylic acid with alkylchloroformate, followed by aminolysis of the obtained mixed anhydride with alkanolamine.

Procedure:

a carboxylic acid solution in a suitable organic solvent, selected from the group consisting of ketones, esters, ethers, chlorinated solvents, dialkylamides , dialkylsulphoxides and heterocycles, is cold stirred at a temperature ranging from -20°C to +30°C. An equivalent quantity of alkylchloroformate is added slowly, over a period of 30 min to 3 hrs.

Activation is carried out in the presence of a suitable weak base, selected from the group consisting of inorganic carbonates and bicarbonates and organic tertiary amines, at a temperature ranging from - .20°C to +30°C.

The obtained mixed anhydride is subjected to aminolysis by addition of an equivalent quantity of alkanolamine, still at low temperature.

The alkanolamide obtained is purified by a method or by a combination of methods as per Method A.

Some preparation examples of the compounds of formulas (I) and (II) according to the present invention and their biological activities are reported hereinbelow for illustrative but not limitative purposes.

Example 1: Preparation of N-(2-hydroxyethyl)-palmitoylamide

Following the method described by Roe et al. (J. Am. Chem. Soc . , 74, 3442-3443, 1952), palmitic acid (2.56 g; 1 mmol) was caused to react with ethanolamine (0.9 g; 1.5 mmol) by refluxing in ethyl ether, under nitrogen atmosphere, for 5 to 6 hrs. The product obtained was extracted from the reaction mixture and crystallized from 95% ethyl alcohol at 0°C.

The physico-chemical properties of N-(2-hydroxyethyl)- palmitoylamide were as follows:

Example 2: Preparation of N-(2-acetoxyethyl)-palmitoylamide

N-(2-hydroxyethyl)-palmitoylamide (see Example 1) (3-0 g; 10 mmol) was solubilized in anhydrous pyridine (30 ml) under stirring at 0°C and added with acetic anhydride (1.53 g; 15 mmol). The resulting solution was stirred at 0°C for a period of 15 min and heated to 45°C for 24 hrs. The reaction mixture was evaporated to dryness in vacuo. The residue was taken up with methanol (30 ml) and evaporated to dryness in vacuo. The residue was crystallized from methanol (50 ml) and the crystalline fraction was separated by filtration, washed three times with cold methanol (10x3 ml) and finally dried in high vacuo.

The reaction yield was 93% approx.

The physico-chemical properties of N-(2-acetoxyethyl)-palmitoylamide were as follows:

Example 3: Preparation of N-(2-acetoxyethyl)-benzoylamide

N-(2-hydroxyethyl)-benzoylamide (1.65 g, 10 mmol), prepared according to Example 8 of the European patent application published with No. 0 550 006, was solubilized in anhydrous pyridine (15 nil) under stirring at 0°C and added with acetic anhydride (1.53 g). The resulting solution was stirred at 0°C for a period of 15 min and heated to 45°C for 24 hrs. The reaction mixture was evaporated to dryness in vacuo. The residue was taken up with water (30 ml) and extracted twice with ethyl acetate (20×2 ml). The organic phases were washed twice with 1N C1 (10x2 ml), once with water (10 ml), twice with 5% NaCOH₃ (10×2 ml) and once with water (10 ml). They were then combined, dehydrated with Na₂SO₄, evaporated to dryness in vacuo. The residue was crystallized from tert-butylmethyl ether (20 ml) and the crystalline fraction was separated by filtration, washed twice with cold tert-butylmethyl ether (5×2 ml) and finally dried in high vacuo.

The reaction yield was 85% approx.

The physico-chemical properties of N-(2-acetoxyethyl)- benzoylamide were as follows:

Example 4: Preparation of N,N'-bis(2-acetoxyethyl)-fumaroylamide

N,N'-bis(2-hydroxyethyl)-fumaroyldiamide (2.02 g; 10 mmol), prepared according to Example 1 of the European patent application published with No. 0 550 008, was solubilized in anhydrous pyridine (20 ml) under stirring at 0°C and added with acetic anhydride (3-06 g; 30 mmol). The resulting solution was stirred at 0°C for a period of 15 min and heated to 45°C for 24 hrs. The reaction mixture was evaporated to dryness in vacuo. The residue was taken up with methanol (30 ml) and evaporated to dryness in vacuo. The residue was crystallized from absolute ethanol (50 ml) and the crystalline fraction was separated by filtration, washed three times with cold ethanol (5×3 nil) and finally dried in high vacuo. The reaction yield was 91% approx.

The physico-chemical properties of N,N'-bis(2-acetoxyethyl)- fumaroylamide were as follows:

Example 5: Preparation of N-palmitoylethanolamide phosphate

N-(2-hydroxyethyl)-palmitoylamide (see Example 1) (3-0 g; 10 mmol) was solubilized in anhydrous methanesulphonic acid (10 ml) under stirring at 0°C and added with phosphoric anhydride (2.12 g; 15 mmol). The resulting mixture was stirred at 0°C for a period of 25 hrs. The reaction mixture was added with ether until product precipitation was complete. The precipitate was separated by centrifugation, dried in vacuo, washed with cold water and finally dried in vacuo. The crude product obtained was hot washed with tert-butylmethyl ether (50 ml) and crystallized from isopropanol (50 ml). The crystalline fraction was separated by filtration, washed three times with cold isopropanol (10×3 nil) and finally dried in high vacuo.

The reaction yield was 83% approx.

The physico-chemical properties of N-palmitoylethanolamide phosphate were as follows:

Example 6: Preparation of N,N'-bis(2-hydroxyethyl)-dodecenediamide diphosphate disodium salt

Traumatic acid (2.28 g; 10 mmol) and N-hydroxysuccinimide (2.42 g; 21 mmol) were solubilized in anhydrous pyridine (50 ml) under stirring at 0°C and added with dicyclohexylcarbodiimide (4.33 E , 21 mmol). The resulting mixture was stirred at 0°C for a period of 1 hr and further stirred at room temperature for a period of 20 hrs. The resulting suspension was filtered, the precipitate removed and the solution evaporated to dryness in vacuo. The crude residue was solubilized in DMF (50 ml), added with triethylamine (5.05 g; 50 mmol) and stirred at 0°C. 0-phosphocholamine (2.96 g; 21 mmol) was solubilized in cold water (10 ml) and the resulting solution was added dropwise to the succinimide ester solution over a period of 1 hr. The mixture was further stirred at room temperature for a period of 24 hrs and finally evaporated to dryness in high vacuo. The residue was taken up with water (20 ml) and eluted in a column containing 70 ml of cationic exchange resin Dowex 50×8, generated in the H+ form. The eluate was neutralized to pH 7-0 with 5% Na₂CO₃ solution and concentrated in vacuo to 5 ml by vol. approx. The oily residue was purified by reverse phase chromatography in Lichrosorb RP18 R column, eluting with water. The fractions containing the pure product were combined and lyophilized.

The reaction yield was 78% approx.

The physico-chemical properties of N,N'-bis-(2-hydroxyethyl)- dodecenediamide diphosphate disodium salt were as follows:

Example 1 : Preparation of N-(2-hydroxyethyl)-palmitoylamide succinate acid

N-(2-hydroxyethyl)-palmitoylamide (3-0 g; 10 mmol) (see Example 1) was added with succinic anhydride (1.5 gϊ 15 mmol) and anhydrous sodium acetate (50 mg). The mixture was heated to 120°C with continued stirring, under nitrogen atmosphere, and cooled to room temperature. The crude product obtained was crystallized from a 0 : 30 ethanol-water mixture ( 50 ml ) . The precipitate was separated by filtration , washed three times with cold ethanol ( 10×3 ml ) and finally dried in high vacuo .

The reaction yield was 94% approx.

The physico-chemical properties of N- (2-hydroxyethyl ) - palmitoylamide succinate acid were as follows :

Example 8: Preparation of N,N'-bis(2-hydroxyethyl)-dodecenediamide disuccinate acid

N,N'-bis(2-hydroxyethyl)-dodecenediamide (3.14 g; 10 mmol) prepared according to Example 6 of the European patent application published with No. 0 550 008, was added with succinic anhydride (3.0 g; 30 mmol) and anhydrous sodium acetate (100 mg). The mixture was heated to 120°C for 3 hrs with continued stirring, under nirrogen atmosphere, and cooled to room temperature. The crude product obtained was crystallized from a 70:30 ethanol-water mixture (50 ml). The precipitate was separated by filtration, washed three times with cold ethanol (10×3 ml), and dried in high vacuo.

The reaction yield was 89% approx.

The physico-chemical properties of N,N'-bis(2-hydroxyethyl)- dodecenediamide disuccinate acid were as follows:

Example 9: Preparation of N,N'-bis-(2-hydroxyethyl)-nonandiamide

A mixture of acrylic acid (1.88 g; 10 mmol) and ethanolamine (1.84 g; 30 mmol) was fed to a flask provided with reflux condenser and heated to 160°C, for 6 hrs, on an oil bath.

The reaction mixture was crystallized from isopropanol (50 ml). The crystalline fraction was separated by filtration, washed three times with cold isopropanol and finally dried in high vacuo.

The reaction yield was 78% approx.

The physico-chemical properties of N,N'-bis(2-hydroxyethyl)- nonandiamide were as follows:

Example 10: Preparation of N-(2-hydroxyethyl)-arachidonamide

A mixture of arachidonic acid (3-04 g; 10 mmol) and triethanolamine (10.6 g; 10.5 mmol) in anhydrous THF (100 ml) was stirred under nitrogen atmosphere, added dropwise over a period of 30 minutes to a solution of isobutylchloroformate (1.44 g; 10.5 mmol) in THF (50 ml). The resulting mixture was stirred at -10°C for 2 hrs and then at 0°C for 5 hrs, and added dropwise with ethanolamine (0.9 g; 14.7 mmol). The resulting mixture was stirred at 0°C for over 2 hrs and finally evaporated to dryness. The crude residue was purified by chromatography eluting with a

98:2 v/v chloroform-methanol mixture. The eluate fractions were combined and evaporated to dryness; the residue was dried in vacuo.

The physico-chemical properties of N(2-hydroxyethyl)- arachidonamide were as follows:

solubility in organic

BIOLOGICAL ACTIVITY

In vitro evaluation of the neuroprotective effect against excitotoxicity of Excitatory Amino Acids in primary neuronal cultures of the following compounds was carried out:

Compound a: N-(2-hydroxyethyl)-palmitoylamide (Example 1)

Compound b: N-palmitoylethanolamide phosphate (Example 5)

Compound c: N-(2-hydroxyethyl)-arachidonamide (Example 10)

Compound d: N,N'-bis-(2-hydroxyethyl)-nonanediamide (Example 9)

Materials and Methods

Compounds solubilization:

the compounds under evaluation, referred to as a, b, c, and d, were solubilized in DMSO and culture medium to obtain concentrations of 100 μM (4% DMSO) and 60 μM (3% DMSO) and added to the culture mediums according to different treatment schedules in order to determine the time-effect relationship vs. the incubation time and the exposure to the neurotoxic stimulus.

Cultures preparation:

granular cell cultures were obtained from postnatal day 8-9 mouse Balb-6 cerebellum. The cells were suspended in EBM + 2mM L-glutamine, 100 U/ml penicillin, 50 μg/1 gentamicin, 25 mM KCl and 10% fetal calf serum, plated on polylysine substrate, cultured for 8-10 days and then exposed to Glu 500 μM at room temperature for 5 min. The compounds being evaluated were added to the cultures at the same time of exposure, soon after exposure or 15 min after exposure to Glu, and cultured for 60 minutes; cultures were then washed and brought back to the original medium. The number of survived cells was evaluated by colorimetric method (MTT) 24 hours after excitotoxic stimulation.

Results

The tested compounds exert a protective action against the excitotoxic stimulus at the two concentrations tested (100 and 60 uM), independently of the treatment scheme adopted, that is when incubated at the same time of exposure, soon after exposure or 15 min after exposure to Glu, as shown in Table 1. Furthermore, they do not show any significant intrinsic cytotoxicity.

Said experimental evidences suggest that the aforesaid molecules exert a protective action within very short times and affect not only the cytotoxic events mediated by an overstimulation of NMDA receptor, but above all, being active during post-treatment, the cytotoxic mechanisms following receptor activation, thus concurring for example to limit calcium ions influx into the cell and the consequent processes leading to cellular death.

Conclusions

As a whole, the above experimental evidences show that N-acyl derivatives of mono and dicarboxylic acids with amino alcohols according to the present invention are able, even at low concentrations, to exert a specific protective action against the neurotoxicity of Excitatory Amino Acids on neuronal cells. Particular notice has to be given to the outstanding therapeutic significance of said molecules, in that i) they are characterized by an extremely prompt effect and ii) they are active when administered at the same time or more importantly after exposure to excitatory amino acids, thus affecting not only the short-term neurotoxic mechanisms mediated by the activation of glutamic or kainic acid receptors, but also one or more events downstream of receptor overstimulation. Furthermore, the compounds do not show any significant intrinsic cytotoxicity.

Therefore, the derivatives described herein can be advantageously used in the treatment of CNS disorders of humans and animals, whose etiology/evolution is associated with the hyper stimulation of excitatory amino acid receptors, in particular the NMDA receptor.

In fact, under physiological conditions, Ecitatory Amino Acids (EAA) mediate synaptic transmission, involved in the phenomena of neuronal plasticity underlying behavioural and cognitive processes, and in motor functions. Under particular conditions of hyper stimulation, they are responsible for a neuronal damage that may ultimately result in neuronal death. There is evidence for a correlation between overstimulation of NMDA receptors and CNS damage associated with acute events, such as hypoxia-ischaemia, stroke, hypoglycaemia, perinatal anoxia, epilepsy, brain and spinal cord injuries, neurolathyrism, or in chronic neurodegenerative disorders, such as Hungtington' s Chorea, Alzheimer's and Parkinson's diseases, amyotrophic lateral sclerosis, and pontocerebellar degeneration (J.W. Olney, "Excitotoxic Amino Acids and Neuropsychiatric Disorders", Ann. Rev. Pharmacol. Toxicol., 30: 47-71, 1990) or neurological complications associated with viral diseases, such as HIV-1 infection (AIDS dementia complex) (M.P. Heyes et al., "Quinolinic Acid in Cerebrospinal fluid and serum in HIV-1 Infection: Relationship to Clinical and Neurological Status", Ann. Neuro l., 29: 202-209, 1991). Further disturbances of the glutamatergic system are known to have a remarkable consequence for hypothalamic homeostasis and on processes derived therefrom (A.N. Van den Pol and P.Q. Trombley, "Glutamate Neurons in Hypothalamus regulate Excitatory Transmission", The J. of Neuroscience , 13(7): 2829-2836, 1993).

It should be emphasized that currently available therapies are of limited value in the acute phase of diseases such as cerebral ictus, which have an extremely narrow "therapeutic window" in terms of the time frame during which neuronal cell death can be limited by pharmacological intervention. In this context, it is of great significance that the molecules of the present invention are capable of acting not only within this very short time of damage induction, but also later on when the damage has been already established. Further, since said new derivatives do not act like NMDA-receptor competitive or non-competitive inhibitors, they may effectively be used also to treat chronic diseases such as Hungtington's Chorea, Parkinson's disease and conditions involving dementia without affecting plastic phenomena and thus, unlike NMDA receptor inhibitors, would not be expected to worsen the clinical outcome.

It needs to be remembered that dosages, times and routes of administration will vary depending on the disease type, stage and severity. A distinction is to be made between treatment of:

i) acute conditions (hypoxia-ischaemia, stroke, brain and spinal cord injury, hypoglycaemia, cerebral hypoxic states associated with cardiovascular surgery) or diseases inducing a prompt and massive Glu release, such as epilepsy, transient ischaemic attacks (TIA), neurolathyrism; ii) chronic degenerative diseases such as Hungtington's Chorea, Alzheimer's and Parkinson's diseases, amyotrophic lateral sclerosis and dementia, either primary or associated with other pathologies even of viral origin, such as acquired immunodeficiency syndrome (AIDS dementia complex).

Further, primary retinic diseases even of anoxic nature or associated with eye hypertension, e.g. glaucoma, are to be taken into consideration. For all aforesaid diseases, the compounds according to the present invention can be administered by systemic oral or parenteral routes, or by topical or transdermic routes.

The therapeutic dose varies, depending on the patient's age and weight as well as on the type of disease, from 0.1 to 100 mg/kg/die, preferably from 1 to 30 mg/kg/die, over variable periods depending on the disease, in any case for at least 30 days.

The pharmaceutical compositions are inclusive of all formulations containing pharmaceutically acceptable excipients, that are suitable for the administration of the claimed active ingredients in the forms best suited to the disease to be treated and, in any case, rendering the active ingredients as bioavailable as possible. In particular, injectable solutions for general intravenous, subcutaneous and intramuscular administration and solutions for ophthalmic treatment are to be envisaged. As concerns the formulations per os granular powders, tablets, pills and capsules are the preferred ones. Example 1: Tablets

Every tablet contains:

Example 2: Vials for injection

Every vial contains:

lyophilized N,N'-bis-

Example 3: Gelatin capsules

Every capsule contains:

Example 4: Gel for ophtalmic use

Every tube contains 5 g of product having the following composition: w/w

In conclusion, the compounds of the present invention, when adequately formulated, may be conveniently used in human and animal therapy for the treatment of diseases in which acute or chronic neurological damage is directly or indirectly due to excitotoxic phenomena, such as caused by Glu or related toxins. Said diseases are e.g.: hypoxic and/or ischaemic cerebral insults, hypoxic and/or ischaemic acute or recurrent and transient attacks, such as TIA; brain or spinal cord injuries; neurodegenerative disorders of unknown etiology (Alzheimer's and Parkinson's diseases, Huntington's Chorea, amyotrophic lateral sclerosis), or derived from neuronal disturbances following epilepsy and severe hypoglycaemic states; neurological complications whose primary cause is an infection (e.g. HIV); neurological complications following hypoxic states caused by cardiovascular surgery or heart failure; diseases pertaining to the retina and in general to the visual system, as well as pertaining to other cranial nerves, e.g. nerves afferent to the auditory system, and neurological diseases following excitotoxic damage due to toxic agents e.g. neurolathyrism.

Claims

1. Use of N-acyl derivatives of aminoalcohols of formula (I)

where is

the acyl radical of a saturated or unsaturated aliphatic monocarboxylic acid, containing 2 to 20 carbon atoms, optionally substituted in the aliphatic chain with one of more hydroxyl, aminic, ketonic, carboxyl, cycloalkyl, aryl, heterocyclic, aromatic, heteroaromatic, polycyclic groups, or

the acyl radical of an aromatic, heteroaromatic or heterocyclic monocarboxylic acid;

R₂ is an alcoholic residue selected from a C₁-C₂₀ linear or branched hydroxyalkyl, optionally substituted in the aliphatic chain with one or more aryl groups, and a hydroxyaryl optionally substituted with one or more linear or branched alkyl radicals of from 1 to 20 carbon atoms; the hydroxyl group of R₂ being optionally esterified to -OX, wherein X is the acyl radical of a linear or branched, saturated or unsaturated aliphatic acid, optionally substituted in the aliphatic chain with one or more aryl groups or with one -COOH optionally salified, or X is the acyl radical of an aromatic acid or -PO₃H₂ optionally salified;

R₃ is H or R₂;

as active principles in the preparation of pharmaceutical compositions for the prevention and treatment of neurological disorders connected with excitotoxicity.

2. The use according to claim 1, wherein said aliphatic monocarboxylic acid is selected from the group consisting of acetic, caproic, butyric, lauric, palmitic, myristic, stearic, oleic, linoleic, linolenic, pyruvic, lactic, caprylic, valeric, valproic, arachidonic acids, gamma¬trimethoxybutyrobetaine and derivatives thereof acylated on the hydroxyl group.

3. The use according to claim 1, wherein said aromatic, heteroaromatic or heterocyclic monocarboxylic acid is selected from the group consisting of salicylic, acetylsalicylic, benzoic, trimethoxybenzoic, isonicotinic , thenoic, phenylanthranilic , retinoic, hydroxyphenylacetic , α-lipoic and deoxycholic acids.

4. The use according to claim 1, wherein said aminoalcohol is selected from the group consisting of ethanolamine, diethanolamine, 2-hydroxypropylamine and di-(2-hydroxypropyl)-amine.

5. The use according to claim 4, wherein 2-hydroxypropylamine and di-(2-hydroxypropyl)-amine are racemic or optical isomers.

6. The use according to claim 1, wherein X is selected from the group consisting of ,

, -PO₃H₂, ,

and salified derivatives thereof with K, Na, Mg and Ca.

7. The use according to claim 1, wherein said disorders are selected from the group consisting of hypoxic-ischaemia, stroke, brain and spinal cord injuries, epilepsy, transient ischaemic attacks, neurolathyrism, amyotrophic lateral sclerosis, Hungtington's Chorea, Alzheimer's disease, primary dementia, dementia connected with viral infections and anoxic ischaemic diseases of the retina.

8. The use according to claim 1, wherein said pharmaceutical compositions are orally administered in the form of granular powders, tablets, pills or capsules.

9. The use according to claim 1, wherein said pharmaceutical compositions are administered by intravenous, subcutaneous or intramuscular routes.

10. The use according to claim 1, wherein said pharmaceutical compositions are suitable for ophthalmic use in the form of drops or ointments.

11. The use according to claim 1, wherein said pharmaceutical compositions are topically or transdermically administered.

12. The use according to claim 1, wherein said active principle is administered at a dosage ranging from 0.1 to 100 mg/kg/die, for at least

30 days.

13. The use according to claim 12, wherein said dosage ranges from 1 to

30 mg/kg/die.

14. Use of N-acyl derivatives of aminoalcohols of formula (II)

where is

a diacyl radical of a saturated or unsaturated aliphatic dicarboxylic acid , optionally substituted with an aminic , hydroxyl , ketonic , or a diacyl radical of an aromatic , heterocyclic or heteroaromatic dicarboxylic acid;

R₂ and R₅ are alcoholic residues selected from a C₁-C₂₀ linear or branched hydroxyalkyl, optionally substituted with one or more aromatic groups, and a hydroxyaryl optionally substituted with one or more linear or branched alkyl radicals of from 1 to 20 carbon atoms; the hydroxyl group of R₂ being optionally esterified to -OX, wherein X is the acyl radical of a linear or branched, saturated or unsaturated aliphatic acid, optionally substituted in the aliphatic chain with one or more aryl groups or with one -COOH optionally salified, or X is the acyl radical of an aromatic acid or -PO₃H₂ optionally salified;

R₃ and R₆ are H or have the same meaning as R₂ and R₅;

15. The use according to claim 14, wherein said aliphatic dicarboxylic acid is selected from the group consisting of oxalic, fumaric, azelaic, succinic, traumatic, glutaric, muconic, malic, aspartic and tartaric acid.

16. The use according to claim 14, wherein said aromatic, heteroaromatic or heterocyclic dicarboxylic acid is selected from the group consisting of phthalic, folic and chromoglycic acid.

17. The use according to claims 14 , wherein said aminoalcohol is selected from the group consisting of ethanolamine, diethanolamine, 2-hydroxypropylamine and di-(2-hydroxypropyl)amine.

18. The use according to claim 17, wherein 2-hydroxypropylamine and di-(2-hydroxypropyl)-amine are racemic or optical isomers.

19. The use according to claim 14, wherein X is selected from the group consisting of ,

, -PO₃H₂ , ,

and salified derivatives thereof with K, Na, Mg and Ca.

20. The use according to claim 14, wherein said disorders are selected from the group consisting of hypoxic-ischaemia, stroke, brain and spinal cord injuries, epilepsy, transient ischaemic attacks, neurolathyrism, amyotrophic lateral sclerosis, Hungtington's Chorea, Alzheimer's disease, primary dementia, dementia connected with viral infections and anoxyischaemic diseases of the retina.

21. The use according to claim 14, wherein said pharmaceutical compositions are orally administered in the form of granular powders, tablets, pills or capsules.

22. The use according to claim 14, wherein said pharmaceutical compositions are administered by intravenous, subcutaneous or intramuscular routes.

23. The use according to claim 14, wherein said pharmaceutical compositions are suitable for ophthalmic use, in the form of drops or ointments.

24. The use according to claim 14, wherein said pharmaceutical compositions are topically or transdermically administered.

25. The use according to claim 14, wherein said active principle is administered at a dosage ranging from 0.1 to 100 mg/kg/die, for at least

30 days.

26. The use according to claim 25, wherein said dosage ranges from 1 to 30 mg/kg/die.