Patent Application
20110319463
The present invention relates to a preventive or therapeutic agent for an optic nerve disorder, a retinal nerve cell death inhibitor, or a neurofilament light chain expression level recovering agent comprising at least one of 4,6-dichloro-1H-indole-2-carboxylic acid derivatives or salts thereof as an active ingredient.
A retina is a tissue of 0.1 to 0.5 mm in thickness consisting of 10 layers, namely, an inner limiting membrane, a nerve fiber layer, a ganglion cell layer, an inner plexiform layer, an inner nuclear layer, an outer plexiform layer, an outer nuclear layer, an outer limiting membrane, a photoreceptor cell layer and a retinal pigmented epithelial layer, in which there are retinal nerve cells such as a photoreceptor cell, a bipolar cell, a ganglion cell, a horizontal cell and an amacrine cell.
A retinal nerve cell plays an important role in receiving and transmitting a visual information such as converting an optical stimulation into an electric signal which it then transmits to a brain.
In its transmission mechanism, when discussed in detail, a visual information entering an eye is converted by a photoreceptor cell into an electric signal which is transmitted, via a horizontal cell, a bipolar cell and/or an amacrine cell, to a ganglion cell. Then, the electric signal is transmitted, via an optic nerve which is a bundle of optic nerve fibers including a ganglion cell axon, to a brain.
When an optic nerve is impaired by various causes, a homeostasis of the optic nerve can not be maintained, resulting in an interference with the transmission of a visual information to a brain, which leads to a vision disorder such as blindness and constriction of visual fields.
While various causes of an optic nerve impairment are considered, a major cause may for example be 1) a rise of intraocular pressure, 2) a retinal blood circulation impairment/retinal ischemia, 3) an increased excitatory amino acid and the like, and these pathologies are accompanied with an activation of a glutamic acid signal cascade or a retinal ganglion cell axon impairment followed by a retinal nerve cell apoptosis, by which the optic nerve is considered to be impaired.
Accordingly, a drug which protects a retinal nerve cell by blocking a part of the glutamic acid signal cascade whereby inhibiting a retinal nerve cell apoptosis, i.e., a drug such as a glutamic acid neurotoxicity inhibitor, an N-methyl-D-aspartic acid (hereinafter referred to also as “NMDA”) receptor blocker, a nitrogen monoxide synthesis inhibiting agent and the like, is considered to be useful as a preventive or therapeutic agent for an optic nerve disorder or an ophthalmic disease accompanying it, and various studies are undertaken currently.
For example, those disclosed are a retinal nerve cell protecting agent comprising as an active ingredient one of β blockers, namely, nipradilol, in Patent Document 1, an optic ganglion cell protecting agent comprising as an active ingredient an interleukin-1 receptor antagonist protein in Patent Document 2, a optic ganglion cell protecting agent comprising as an active ingredient an αl receptor blocker such as bunazosin in Patent Document 3, a retinal nerve cell protecting agent comprising as an active ingredient a fluorine-containing prostaglandin F2α derivative in Patent Document 4, and a retinal nerve cell protecting agent comprising as an active ingredient an indazole derivative in Patent Document 5.
Representative ophthalmic diseases accompanied with optic nerve disorders may for example be glaucomatous diseases, retinal diseases, ischemic disorders and the like such as glaucoma, glaucomatous constriction of visual fields, glaucomatous optic nerve atrophy, glaucomatous optic neurosis, central retinal artery occlusion, branch retinal arterial occlusion, central retinal vein occlusion, branch retinal venous occlusion, diabetic retinopathy, macular degeneration (age-related macular degeneration such as atrophic age-related macular degeneration, exudative age-related macular degeneration and the like), retinitis pigmentosa, retinopathy of prematurity, retinal detachment, retinal pigment epithelial detachment, Leber disease, ischemic optic neurosis and the like.
On the other hand, sodium (E)-4,6-dichloro-3-(3-oxo-3-(phenylamino)-1-propenyl)-1H-indole-2-carboxylate (GV-150526A) which is one of 4,6-dichloro-1H-indole-2-carboxylic acid derivatives or salts thereof is described in Patent Document 1 and Patent Document 2 as an excitatory amino acid antagonistic agent useful as a therapeutic agent for Alzheimer disease, Huntington disease, amyotrophic lateral sclerosis and the like.
In addition, sodium (E)-4,6-dichloro-3-((2-oxo-1-phenyl-3-pyrrolidinylidene)methyl)-1H-indole-2-carboxylate (GV-196771A) which is one of 4,6-dichloro-1H-indole-2-carboxylic acid derivatives or salts thereof is described in Patent Document 3 as an antagonist of NMDA useful as a therapeutic agent for Alzheimer disease, Huntington disease, amyotrophic lateral sclerosis and the like.
Also in Patent Document 4,4,6-dichloro-1H-indole-2-carboxylic acid derivative or a salt thereof is described as an indole derivative which has a sphingosine-1-phosphate (hereinafter referred to also as “S1P”) receptor agonistic and/or antagonistic activity and is useful as a therapeutic agent for a glaucoma, a dry eye, a vascularization, a cardiovascular disease and the like.
Nevertheless, the preventive or therapeutic effect of a 4,6-dichloro-1H-indole-2-carboxylic acid derivative or a salt thereof on an optic nerve disorder is not described expressly or specifically in these Patent Document.
It is a very interesting objective to discover a compound useful as a preventive or therapeutic agent for an optic nerve disorder, a retinal nerve cell death inhibitor, or a neurofilament light chain expression level recovering agent, especially to discover a compound which exerts said pharmacological effect by an oral administration or an ophthalmic local administration.
Inventors investigated an enormous number of compounds for an efficacy in an NMDA-induced rat retinal disorder model for the purpose of discovering a compound useful as a preventive or therapeutic agent for an optic nerve disorder, a retinal nerve cell death inhibitor, or a neurofilament light chain expression level recovering agent. As a result, it was discovered that a 4,6-dichloro-1H-indole-2-carboxylic acid derivative or a salt thereof is:
1) capable, when given orally in an NMDA-induced rat retinal disorder model, of inhibiting a reduction in the cell count in its retinal nerve cell layer;
2) capable, when given intravitreously in an NMDA-induced rat retinal disorder model, of recovery from a reduction in the expression level of the neurofilament light chain (one of major constituents of the optic nerve axon and a component important in maintaining the morphology of the optic nerve axon) in the retina; and,
3) free of, or capable of reducing, a side effect, such as a weight gain inhibiting effect, observed when using other NMDA receptor blockers such as memantine; thus establishing the present invention.
Thus, the present invention relates to a preventive or therapeutic agent for an optic nerve disorder, especially to a preventive or therapeutic agent which is free of, or capable of reducing, a side effect such as a weight gain inhibiting effect, comprising as an active ingredient at least one of the compound represented by Formula (1):
wherein R1 is a hydrogen atom or a lower alkyl group;
R2 is a hydrogen atom or a lower alkyl group;
R1 and R2 may be joined each other to form an aziridine ring, an azetidine ring, a pyrrolidine ring, a piperidine ring or an azepane ring; and
R3 is a carboxyl group or an ester thereof or an amide thereof, hereinafter being applicable similarly; or a salt thereof (hereinafter referred to as “the present compound”).
The definitions of the terms employed in the specification are described in detail below.
A “halogen atom” refers to a fluorine, chlorine, bromine or iodine atom.
A “lower alkyl group” refers to a straight or branched alkyl group having 1 to 8, preferably 1 to 6, especially 1 to 4 carbon atoms. The typical examples thereof include methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, isopropyl, isobutyl, sec-butyl, tert-butyl, isopentyl groups and the like.
A “halogeno lower alkyl group” refers to a lower alkyl group substituted with one or a plurality of (preferably 2 or 3) halogen atoms. The typical examples thereof include trifluoromethyl, difluoromethyl groups and the like.
An “aryl group” is a residue resulting from removal of one hydrogen atom from a C6-C14 monocyclic aromatic hydrocarbon or dicyclic or tricyclic fused polycyclic aromatic hydrocarbon. The typical examples thereof include phenyl, naphthyl, anthryl, phenanthryl groups and the like.
A “lower alkoxy group” refers to a group resulting from substitution of a hydrogen atom in a hydroxy group with a lower alkyl group. The typical examples thereof include methoxy, ethoxy, n-propoxy, n-butoxy, n-pentoxy, n-hexyloxy, n-heptyloxy, n-octyloxy, isopropoxy, isobutoxy, sec-butoxy, tert-butoxy, isopentoxy groups and the like.
A “halogeno lower alkoxy group” refers to a lower alkoxy group substituted with one or a plurality of (preferably 2 or 3) halogen atoms. The typical examples thereof include trifluoromethoxy, difluoromethoxy groups and the like.
A “lower alkyl group optionally having a substituent” refers to an unsubstituted lower alkyl group and a lower alkyl group having a substituent. The lower alkyl group having a substituent refers to a lower alkyl group substituted with one or a plurality of (preferably 2 or 3) groups selected from the group consisting of a halogen atom, a lower alkyl group, a halogeno lower alkyl group, an aryl group, a lower alkoxy group and a halogeno lower alkoxy group.
An “aryl group optionally having a substituent” refers to an unsubstituted aryl group and a aryl group having a substituent. The aryl group having a substituent refers to an aryl group substituted with one or a plurality of (preferably 2 or 3) groups selected from the group consisting of a halogen atom, a lower alkyl group, a halogeno lower alkyl group, a lower alkoxy group and a halogeno lower alkoxy group.
An “ester of a carboxy group” refers to a group represented by Formula (2):
wherein R4 is a hydrogen atom, a lower alkyl group optionally having a substituent or an aryl group optionally having a substituent.
An “amide of a carboxy group” refers to a group represented by Formula (3):
wherein R5 and R6 are same or different and each is a hydrogen atom, a lower alkyl group optionally having a substituent or an aryl group optionally having a substituent.
As used herein, “plurality” means those which are same to or different from each other, the number of which is preferably 2 or 3, especially 2.
A “salt” in the present compound is not limited particularly as long as it is a pharmaceutically acceptable salt, and may for example be a salt with an inorganic acid such as hydrochloric acid, hydrobromic acid, hydroiodic acid, nitric acid, sulfuric acid, phosphoric acid and the like, a salt with an organic acid such as acetic acid, fumaric acid, maleic acid, succinic acid, citric acid, tartaric acid, adipic acid, gluconic acid, glucoheptoic acid, glucuronic acid, terephthalic acid, methanesulfonic acid, lactic acid, hippuric acid, 1,2-ethanedisulfonic acid, isethionic acid, lactobionic acid, oleic acid, pamoic acid, polygalacturonic acid, stearic acid, tannic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, lauryl sulfate, methyl sulfate, naphthalenesulfonic acid, sulfosalicylic acid and the like, a quaternary ammonium salt with methyl bromide, methyl iodide and the like, a salt with a halogen ion such as bromine ion, chlorine ion, iodine ion and the like, a salt with an alkaline metal such as lithium, sodium, potassium and the like, a salt with an alkaline earth metal such as calcium, magnesium and the like, a metal salt with iron, zinc and the like, a salt with ammonia, a salt with an organic amine such as triethylenediamine, 2-aminoethanol, 2,2-iminobis(ethanol), 1-deoxy-1-(methylamino)-2-D-sorbitol, 2-amino-2-(hydroxymethyl)-1,3-propanediol, procaine, N,N-bis(phenylmethyl)-1,2-ethanediamine and the like.
When the present compound has a geometric isomer and/or an optical isomer, such an isomer is also encompassed within the scope of the present compound.
When the present compound has a proton tautomerism, its tautomers (keto form, enol form) are also encompassed within the scope of the present compound.
When the present compound has a hydrate and/or a solvate, such a hydrate and/or a solvate is also encompassed within the scope of the present compound.
When the present compound has a polymorphism and a polymorphic group (polymorphic system), its polymorphic form and polymorphic group (polymorphic system) are also encompassed within the scope of the present compound. As used herein, the polymorphic group (polymorphic system) means crystal forms in respective stages over a course of change in the crystal form depending on the condition and the state (which includes a formulated state) of crystal production, precipitation, storage and the like, as well as the entire of such a course.
(a) As an example of the present compound, a compound or a salt thereof in which respective groups in a compound represented by Formula (1) or a salt thereof are the groups shown below can be given.
(a1) R1 is a hydrogen atom or a lower alkyl group; and/or,
(a2) R2 is a hydrogen atom or a lower alkyl group; and/or,
(a3) R1 and R2 may be joined each other to form an aziridine ring, an azetidine ring, a pyrrolidine ring, a piperidine ring or an azepane ring; and/or,
(a4) R3 is a carboxyl group or an ester thereof or an amide thereof.
Thus, a compound resulting from every combination selected from the abovementioned (1a), (2a), [or (3a)] and (4a) in a compound represented by Formula (1) or a salt thereof.
(b) As a preferred example of the present compound, a compound or a salt thereof in which respective groups in a compound represented by Formula (1) or a salt thereof are the groups shown below can be given.
(1b) R1 is a hydrogen atom; and/or,
(2b) R2 is a hydrogen atom; and/or,
(3b) and R2 may be joined each other to form a pyrrolidine ring; and/or,
(4b) R3 is a carboxyl group.
Thus, a compound or a salt thereof resulting from every combination selected from the abovementioned (1b), (2b), [or (3b)] and (4b) in a compound represented by Formula (1) or a salt thereof.
A compound or a salt thereof which meets with the combination of these (b) requirements with the abovementioned (a) requirements is within the scope of the present compound.
As a preferred typical example of the present compound, the following compounds and salts thereof can be given.
As an especially preferred typical example of the present compound, the following compounds and salts thereof can be given.
Sodium (E)-4,6-dichloro-3-(3-oxo-3-(phenylamino)-1-propenyl)-1H-indole-2-carboxylate (Compound A′, GV-150526A), or,
sodium (E)-4,6-dichloro-3-((2-oxo-1-phenyl-3-pyrrolidinylidene)methyl)-1H-indole-2-carboxylate (Compound B′,GV-196771A).
A preventive or therapeutic agent for an optic nerve disorder, a retinal nerve cell death inhibitor, or a neurofilament light chain expression level recovering agent containing at least one of the present compounds, preferably one of the present compounds as an active ingredient is the present invention.
An “optic nerve disorder” in the invention means an optic nerve disorder and/or an ophthalmic disease accompanied with an optic nerve disorder.
While an “ophthalmic disease accompanied with an optic nerve disorder” as used herein is not limited particularly as long as it is an ophthalmic disease accompanied with an optic nerve disorder and may for example be glaucomatous diseases, retinal diseases, ischemic disorders and the like, the typical examples thereof include glaucoma, glaucomatous constriction of visual fields, glaucomatous optic nerve atrophy, glaucomatous optic neurosis, central retinal artery occlusion, branch retinal arterial occlusion, central retinal vein occlusion, branch retinal venous occlusion, diabetic retinopathy, macular degeneration (age-related macular degeneration such as atrophic age-related macular degeneration, exudative age-related macular degeneration and the like), retinitis pigmentosa, retinopathy of prematurity, retinal detachment, retinal pigment epithelial detachment, Leber disease, ischemic optic neurosis and the like.
While a “glaucomatous optic nerve disorder” in the invention is not limited particularly as long as it is an optic nerve disorder originated from a glaucoma and typically means a glaucoma and/or an ophthalmic disease accompanying a glaucoma, more typical examples thereof include glaucomatous optic nerve disorders such as glaucoma, glaucomatous constriction of visual fields, glaucomatous optic nerve atrophy, glaucomatous optic neurosis and the like.
A “retinal nerve cell” in the invention means a nerve cell involved in the transmission of a visual signal to a brain, and typically means a photoreceptor cell, a horizontal cell, a bipolar cell, an optic ganglion cell, an amacrine cell and the like.
A “retinal nerve cell death” in the invention means an apoptosis and/or a necrosis of a retinal nerve cell.
A “neurofilament light chain expression level recovering agent” in the invention means an agent which inhibits the reduction of and/or increases the expression level of the neurofilament light chain in a retina. This neurofilament light chain is one of major constituents of the optic nerve axon, and is a component important in maintaining the morphology of the optic nerve axon.
This compound can be administered orally or parenterally. The administration mode may for example be an oral administration, an ophthalmic local administration (instillation, administration into conjunctival sac, intravitreous administration, subconjunctival administration, administration into Tenon's capsule and the like), intravenous administration, percutaneous administration and the like, and a pharmaceutically acceptable additive may appropriately be selected and used if necessary to formulate a dosage form suitable to the administration mode.
The dosage form may for example be a tablet, a capsule, a granule, a powder and the like for an oral formulation and an injection formulation, an eye drop, an ointment, a patch, a gel, an insert and the like for a parenteral formulation.
In case for example of a tablet, a capsule, a granule, a powder and the like, those which can appropriately be selected and used if necessary to formulate a dosage form are excipients such as lactose, glucose, D-mannitol, anhydrous calcium hydrogen phosphate, starch, sucrose and the like; disintegrants such as carboxymethyl cellulose, calcium carboxymethyl cellulose, sodium crosscarmelose, crosspovidon, starch, partially alphatized starch, low-substituted hydroxypropyl cellulose and the like; binders such as hydroxypropyl cellulose, ethyl cellulose, gum arabic, starch, partially alphatized starch, polyvinyl pyrrolidone, polyvinyl alcohol and the like; lubricants such as magnesium stearate, calcium stearate, talc, hydrated silicon dioxide, hardened oil and the like; coatings such as purified sugar, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, methyl cellulose, ethyl cellulose, polyvinyl pyrrolidone and the like; flavors such as citric acid, aspartame, ascorbic acid, menthol and the like.
An injection formulation (aqueous, oily, suspension) can be formulated while selecting and using, appropriately if necessary, an isotonicity-imparting agent such as sodium chloride and the like; a solvent or solubilizing agent such as a soybean oil, Macrogol and the like; a buffering agent such as sodium phosphate and the like; a surfactant such as Polysorbate 80 and the like; a thickening agent such as sodium carmelose, methyl cellulose and the like; an analgesic agent such as benzyl alcohol and the like, and its pH may be any value within a range acceptable for an injection formulation, and is preferably within a range from pH4 to 8.
An eye drop (aqueous, oily, suspension) can be formulated while selecting and using, appropriately if necessary, a solvent or solubilizing agent such as castor oil, glycerol, alcohol, an ether compound between a polyglycerol and an alcohol and the like; an isotonicity-imparting agent such as sodium chloride, conc. glycerin and the like; a buffering agent such as phosphates, carbonates and the like; a surfactant such as polyoxyethylene sorbitan monooleate, polyoxyl stearate 40, polyoxyethylene hardened castor oil and the like; a stabilizer such as sodium citrate, sodium edetate and the like; a preservative such as benzalkonium chloride, paraben and the like; and, in the case of an eye drop suspension, a dispersant such as a water-soluble polymer and the like, an isotonicity-imparting agent such as sodium chloride, conc.glycerin and the like; a buffering agent such as phosphates, carbonates and the like; a surfactant such as Polysorbate 80, polyoxyl stearate 40, polyoxyethylene hardened castor oil 60 and the like; a stabilizer such as sodium citrate, sodium edetate and the like; a preservative such as benzalkonium chloride, paraben and the like, and its pH may be any value within a range acceptable for an ophthalmologic eye drop formulation, and is preferably within a range from pH 4 to 8.
An ophthalmic ointment can be formulated using a commonly employed base material such as a white petrolatum, a liquid paraffin and the like.
An insert can be formulated using a biodegradable polymer such as hydroxypropyl cellulose, hydroxypropyl methyl cellulose, carboxyvinyl polymer, polyacrylic acid and the like while selecting and using, appropriately if necessary, an excipient, a binder, a stabilizer, a pH modifier and the like.
An intraocular implant formulation can be formulated using a biodegradable polymer such as polylactic acid, polyglycolic acid, lactic acid/glycolic acid copolymer, lactic acid-caprolacton copolymer, polyanhydride, polyorthoester, poly ε-caprolacton and the like, while selecting and using, appropriately if necessary, an excipient, a binder, a stabilizer, a pH modifier and the like. Formulation can be accomplished also by using a non-biodegradable polymer such as an ethylene vinyl acetate copolymer and the like, while selecting and using, appropriately if necessary, an excipient, a binder, a stabilizer and the like.
The dose of the present compound can be selected appropriately depending on the dosage form, the condition, age, body weight of the patient and the like. In the case for example of oral administration, a dosage of 0.01 to 5000 mg, preferably 0.1 to 2500 mg, especially 0.5 to 1000 mg can be administered in portions 1 to several times a day. In the case of injection, a dosage of 0.00001 to 2000 mg, preferably 0.0001 to 1500 mg, especially 0.001 to 500 mg can be administered in portions 1 to several times a day. In the case of an eye drop, a dosage of 0.00001 to 10% w/v, preferably 0.0001 to 5% w/v, especially 0.001 to 1% w/v can be administered 1 to several times a day. An eye ointment containing 0.0001 to 2000 mg can be applied. An insert or intraocular implant containing 0.0001 to 2000 mg can be inserted or implanted.
As described below in detail in the section of a pharmacological test, the present compound was capable, when given orally in an NMDA-induced rat retinal disorder model, of inhibiting a reduction in the cell count in its retinal nerve cell layer. Also it was capable, when given intravitreously in the same model, of recovery from a reduction in the expression level of the neurofilament light chain in a retina.
Accordingly, the present compound is useful as a preventive or therapeutic agent for an optic nerve disorder, a retinal nerve cell death inhibitor, or a neurofilament light chain expression level recovering agent, especially useful as a preventive or therapeutic agent for a glaucomatous optic nerve disorder, more typically, a preventive or therapeutic agent for a glaucomatous ophthalmic disease such as a glaucoma, a glaucomatous constriction of visual fields, a glaucomatous optic nerve atrophy, a glaucomatous optic neurosis and the like, and also useful as a preventive or therapeutic agent which is free of, or capable of reducing, a side effect, such as a weight gain inhibiting effect, observed when using other NMDA receptor blockers such as memantine.
The followings are the results of pharmacological tests and the formulation examples according to the invention. These examples are intended to ensure a better understanding of the invention and are not intended to restrict the scope of the invention.
1. Test Using NMDA-Induced Rat Retinal Disorder Model (Evaluation of Retinal Section after Oral Administration of Test Compound)
A NMDA-induced rat retinal disorder model (Invest. Ophthalmol. Vis. Sci., 2003; 44:385-392) employed widely as an optic nerve disorder model was employed to evaluate the usefulness (retinal nerve cell death inhibiting effect) of the present compound.
A rat [Slc:SD, male, about 7 week-old) was allowed to inhale a gas containing 3 to 4% (v/v) vaporized isoflurane at a rate of 1 to 1.5 L air/min to accomplish a systemic introducing anesthesia, followed by a maintaining anesthesia with 2 to 3% (v/v) isoflurane. Thereafter, 5 μl of a solution of NMDA (Sigma, catalog No. M3262) dissolved at 2 mmol/L in a phosphate buffer (hereinafter referred to also as “PBS”) was given intravitreously (10 nmol as NMDA).
The rat 3 days after the intravitreous administration of the NMDA solution was treated with a 100 mg/kg sodium pentobarbital injection solution by an intraperitoneal administration to accomplish a systemic anesthesia and then the eyeballs were enucleated. The enucleated eyeballs were fixed in a 25%(w/v) glutaraldehyde: 10% (w/v) neutral buffered formalin=1:9 mixture. The fixed eyeballs were embedded with a paraffin and then sliced into retinal sections (3 μm in thickness), which were then subjected to a hematoxylin and eosin staining. Eight retinal sections were taken per eyeball at intervals of 45 μm so that the optic nerve papilla was included. Among these 8 sections, 3 sections were selected randomly, and a selected section was photographed for the retina of 700 to 900 μm in width with its center being located about 1.25 mm from the optic nerve papilla, using which the cell count in the retinal ganglion cell layer (hereinafter referred to also as “GCL cell count”) was calculated (average value). From the resultant GCL cell count, a % GCL cell count reduction inhibition of each test substance was calculated according to Equation 1 while assigning 100% to the non-treatment group and 0% to a group of 10 nmol NMDA given intravitreously+base given orally. Each group included 4 animals (7 to 8 eyeballs).
% GCL cell count reduction inhibition=(NX−NO)/(NU−NO)×100 [Equation 1]
wherein NU is a GCL cell count in the non-treatment group, NO is a GCL cell count in the group of 10 nmol NMDA given intravitreously+base given orally, and Nx is a GCL cell count in the group of 10 nmol NMDA given intravitreously+a test compound given orally.
Over a period from the day of the intravitreous NMDA administration through the eyeball enucleation, each individual animal was weighed once a day. Based on the body weight of the individual animal on the day of the intravitreous NMDA administration, the difference from the body weight on the day of the eyeball enucleation was calculated and the weight gain of each individual animal was calculated (average value). Each group included 4 animals.
5 μL of an NMDA solution dissolved in PBS (10 nmol as NMDA) was administered intravitreously. A 0.5% (w/v) aqueous solution of methyl cellulose was given by a repetitive oral administration twice a day in a volume of 10 mL/kg for 3 days from the day of the intravitreous NMDA administration until 2 days later. On the day of the intravitreous NMDA administration, a 0.5% (w/v) aqueous solution of methyl cellulose was given orally two times which were about 1 hour before the intravitreous NMDA administration and 1 to 2 hours.
5 μL of an NMDA solution dissolved in PBS (10 nmol as NMDA) was administered intravitreously. Each test compound suspended in 0.5% (w/v) methyl cellulose solution was given at a dose of 30 mg/kg by a repetitive oral administration twice a day in a volume of 10 mL/kg for 3 days from the day of the intravitreous NMDA administration until 2 days later. On the day of the intravitreous NMDA administration, each test compound suspended in 0.5% (w/v) methyl cellulose solution was given orally at a dose of 30 mg/kg two times which were about 1 hour before the NMDA administration and 1 to 2 hours.
As a control compound, memantine was employed. 5 μL of an NMDA solution in PBS (10 nmol as NMDA) was administered intravitreously. Memantine dissolved in 0.5% (w/v) methyl cellulose solution was given at a dose of 30 mg/kg by a repetitive oral administration twice a day in a volume of 10 mL/kg for 3 days from the day of the intravitreous NMDA administration until 2 days later. On the day of the intravitreous NMDA administration, memantine dissolved in 0.5% (w/v) methyl cellulose solution was given orally at a dose of 30 mg/kg two times which were about 1 hour before the NMDA administration and 1 to 2 hours.
The results of the test using Compound A′ and Compound B′ as test compounds were shown in Table 1. As evident from Table 1, Compound A′, Compound B′ and a control compound memantine inhibited the reduction in the GCL cell count in the retina which is observed usually in the NMDA-induced rat retinal disorder model.
The results of the weight gain test are shown in Table 2. As evident from Table 2, Compound A′ and Compound B′ allowed for a weight gain almost equivalent to that in the non-treatment group, while memantine inhibited the weight gain when compared with the non-treatment group.
Based on the results of the test, the present compounds including Compound A′ and Compound B′ exhibited a preventive or therapeutic effect on the optic nerve disorders and a retinal nerve cell death inhibiting effect without causing the weight gain inhibition as a side effect when given in the administration mode for a systemic exposure such as an oral administration. They have a preventive or therapeutic effect especially on glaucomatous optic nerve disorders. On the other hand, memantine caused the weight gain inhibition as a side effect although it had similar preventive or therapeutic effect on the optic nerve disorders and retinal nerve cell death inhibiting effect, and accordingly the present compounds are suggested to be more useful in terms of the inhibiting effect described above.
2. Test Using NMDA-Induced Rat Retinal Disorder Model (Quantitative Polymerase Chain Reaction (Hereinafter Referred to Also as “PCR”) Evaluation after Intravitreous Administration of Test Compounds)
In the NMDA-induced rat retinal disorder model, the efficacy of the test compounds were evaluated using as an index the expression level in the retinal tissue of the neurofilament light chain (hereinafter referred to also as “NFL”) which is one of major constituents of the optic nerve axon and is considered to be important in maintaining the morphology of the optic nerve axon.
The rat 1 day after the intravitreous administration of NMDA was treated with a 100 mg/kg sodium pentobarbital injection solution by an intraperitoneal administration to accomplish a systemic anesthesia and then the eyeballs were enucleated, and the retina was isolated. The isolated retina was homogenized, and a total RNA was extracted using QIAzol Lysis Reagent (QIAGEN, catalog No. 79306) and RNeasy 96 Kit (250) (QIAGEN, catalog No. 74106), and then cDNA was synthesized using PrimeScript (trademark) RT reagent Kit (TAKARA, catalog No. RR037B). In accordance with the instruction attached to QuantiTect Multiplex PCR Kit (1000) (QIAGEN, catalog No. 204545), QuantiTect Multiplex PCR Master Mix, the synthesized cDNA, the primers/probe for NFL (Sigma, “Ordermade”) and the primers/probe for glycerylaldehyde 3-phosphate dehydrogenase (hereinafter referred to also as “GAPDH”) (Applied Biosystems, Catalog No. 4352338E) were mixed, and a quantitative PCR machine (Applied Biosystems, Catalog No. 7500-03) was employed to conduct a PCR reaction, whereby measuring the expression levels of NFL and GAPDH.
From the NFL and GAPDH expression levels thus obtained, a relative NFL expression level was calculated by correcting the NFL expression level based on the housekeeping gene GAPDH expression level in accordance with Equation 2. Thereafter, a % NFL recovery of the test compound was calculated based on the NMDA-induced NFL reduction according to Equation 3 while assigning 100% to the non-treatment group and 0% to the 10 nmol intravitreous NMDA group. Each group included 1 animal (2 eyeballs).
The sequences of the primers and the probe for NFL employed in the invention are shown below.
% Relative NFL expression level=(NFL expression level/GAPDH expression level) [Equation 2]
% NFL recovery=(EX−EO)/(EP−EO)×100 [Equation 3]
wherein EP is a relative NFL expression level in the non-treatment group, EO is a relative NFL expression level in the group of 10 nmol intravitreous NMDA administration and EX is a relative NFL expression level in the group of intravitreous administration of 10 nmol NMDA mixed with each compound.
5 μL of an NMDA solution dissolved in a 30% (v/v) DMSO-containing purified water (10 nmol as NMDA) was administered intravitreously.
5 μL of a mixture solution of NMDA and a test compound dissolved in a 30% (v/v) DMSO-containing purified water (10 nmol as NMDA, 15 nmol as a test compound) was administered intravitreously.
The results of the test using Compound A′ and Compound B′ as test compounds were shown in Table 4. As evident from Table 4, Compound A′ and Compound B′ recovered the NFL expression level from the reduction occurring in the NMDA-induced rat retinal disorder model. On the other hand, memantine at the same dose resulted in a recovery from the reduction in the NFL expression level, but its potency was markedly lower than those observed with Compound A′ and Compound B′.
Based on the results of the test, the present compounds including Compound A′ and Compound B′ exhibited a preventive or therapeutic effect on the optic nerve disorders and an NFL expression level recovering effect also when given in the mode for a local administration. On the other hand, memantine had a preventive or therapeutic effect on the optic nerve disorders and retinal nerve cell death inhibiting effect, but the local administration of the same dose gave an efficacy which was markedly weaker than those of Compound A′ or Compound B′, suggesting that the present compounds were stronger in terms of the potential possessed by the compounds themselves.
Representative formulations of the invention are described below.
A tablet formulated as shown above was coated with 3 mg of a coating (for example, a coating such as hydroxypropyl methyl cellulose, Macrogol, talc, titanium oxide, silicone resin and the like) to obtain an intended tablet. Alternatively, the types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired tablet.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired capsule.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired aqueous eye drop.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired oily eye drop.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired eye drop suspension.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired aqueous solution for injection.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired oil for injection.
The types and/or the amounts of the present compound and the additives may appropriately be varied to obtain a desired suspension for injection.
The present compound is useful as a preventive or therapeutic agent for an optic nerve disorder, a retinal nerve cell death inhibitor, or a neurofilament light chain expression level recovering agent, especially useful as a preventive or therapeutic agent for a glaucomatous optic nerve disorder, more typically, a preventive or therapeutic agent for a glaucomatous ophthalmic disease such as a glaucoma, a glaucomatous constriction of visual fields, a glaucomatous optic nerve atrophy, a glaucomatous optic neurosis and the like.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-055998 | Mar 2009 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2010/053940 | 3/10/2010 | WO | 00 | 9/9/2011 |
