AU5953399A

AU5953399A - Remedy for pulmonary heart

Info

Publication number: AU5953399A
Application number: AU59533/99A
Authority: AU
Inventors: Reiji Kasukawa; Hiroshi Koike; Hajimu Kurumatani; Masayuki Miyata; Shintaro Nishio; Yuji Ueno
Original assignee: Toray Industries Inc
Current assignee: Toray Industries Inc
Priority date: 1995-02-27
Filing date: 1999-11-18
Publication date: 2000-02-03
Anticipated expiration: 2016-02-27
Also published as: AU735975B2

Description

AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT: *o Toray Industries, Inc.

*9 o#° ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.

INVENTION TITLE: Remedy for pulmonary heart The following statement is a full description of this invention, including the best method of performing it known to us: Q:%OPERWMKRW7320-96.322 18111199 Q:\OPER\MKR\47320.321 18/11/99 -1A-

DESCRIPTION

AGENT FOR TREATING COR PULMONALE This is a divisional of Application No. 47320/96, the disclosure of which is included herein in its entirety by way of reference.

TECHNICAL FIELD The present invention relates to a method of treating cor pulmonale involving administration of a prostaglandin I2 derivative, for example, beraprost, or a salt thereof as an active ingredient.

BACKGROUND ART Cor pulmonale develops a disease condition in which an S increase in the pulmonary vascular resistance due to an organic or functional abnormality of the lungs causes right ventricular pressure overload, resulting in right ventricular hypertrophy and further right ventricular insufficiency. Cor pulmonale is caused by various diseases, the critical mechanism of ventricular hypertrophy is not clarified, and no curative means is established. Although cor pulmonale is treated by treatment (including oxygen therapy) of a casual disease or using a diuretic and cardiotonic, an effective curative means has not yet been established.

On the other hand, prostaglandin 12 (PGI 2 prostacyclin) which is known as a substance having the strong actions of inhibiting platelet aggregation and dilating the peripheral vessel (refer to "Nature" Vol.

rl- 268, p688, 1976) has an unstable exoenol structure, and thus PGI2 is very unstable in a neutral aqueous solution and is converted into 6-oxo PGF1 a which has substantially no physiological activity. This instability of PGI2 brings about an important problem in utilizing this compound as a medicine. The PGI2 is also unstable in vivo and thus has the fault that its physiological action has no persistency. Japanese Examined Patent Publication No. 1-53672 discloses, as compounds in which the faults of PGI2 are significantly improved, PGI2 derivatives having a skeleton in which the structure of the exoenol ether portion, that is a characteristic structure of PGI2, is converted into an inter-m-phenylene type. However, this publication does not suggest the curative effects of those derivatives on cor pulmonale, and it has not yet been known that the PGI2 derivatives have the curative effects on cor pulmonale.

As a result of extensive research for developing an agent for treating cor pulmonale having excellent efficacy and practicability, the inventors found that the compounds used in the present invention have the significant effect of ameliorating the condition of cor pulmonale, resulting in the achievement of the present invention.

P:\OPER\MKR\SPECI\47320-96.273 30/9/99 -3- DISCLOSURE OF THE INVENTION According to one embodiment of the present invention there is provided a method of treating cor pulmonale comprising administering to a cor pulmonale patient an effective amount of a 5,6,7-trinor-4,8-inter-m-phenylene prostaglandin 12 derivative represented by the following formula

R,

*A

*R2 20

HO

H

20 HO

O

wherein Ri is hydrogen, a carboxyl group or a functional derivative thereof, -CH 2 OH, or a pharmacologically acceptable cation; A is (CH 2

(CH

2 )m-CH=CH- (CH 2 (3)

(CH

2 )p or -CH 2

-O-CH

2 (wherein n is an integer of 0 to 3, and each of m and p is 0 or 1):

R

2 is a straight chain or branched alkyl group having to 10 carbon atoms, -Ct H2t-OR 3 (wherein t indicates an integer of 1 to 5, and R 3 indicates a straight chain or branched alkyl group having 1 to 5 carbon atoms, or a phenyl group), -Ct H2t-CH=C (R 4

(R

5 (wherein t indicates the same as defined above, and R 4 and R 5 each indicate hydrogen, a methyl group, an ethyl group, a propyl group or a butyl group); or -Ct H2t-C=C-Rg (wherein t indicates the same as defined above, and R 6 indicates hydrogen, a methyl group or an P:\OPER\MKR\SPEC\47320-96.273 30/9/99 -4ethyl group); wherein formula indicates 1- and dlforms; or a pharmaceutically acceptable salt thereof.

BEST MODE FOR CARRYING OUT THE INVENTION The inventors of this invention have already found prostaglandin 12 derivatives which are effective as an antiulcer agent, an anti-thrombogenic agent, an antihypertensive agent, and an antiasthmatic agent (Japanese Examined Patent Publication No. 1-53672).

However, this publication does not suggest that these S* derivatives have the curative effect on cor pulmonale, and it has not yet been known that the prostaglandin I2 derivatives have the effect of ameriolating the condition of cor 15 pulmonale. The inventors of this invention first found the effectiveness of the derivatives as an agent for treating cor .pulmonale.

In compounds represented by the above formula RI is preferably a carboxyl group or a functional derivative thereof indicated by -COOR 7 (wherein R 7 is an ester residue, specifically, methyl, ethyl or a pharmacologically acceptable cation such as an alkaline or alkaline earth metal such as sodium, potassium or calcium, an amine such as mono-, di- or trimethylamine, methyl piperidine, mono-, di- or triethanolamine, lysine, or basic amino acid); A is preferably (1) -(CH2)m-CH=CH-(CH2)p-, -(CH)m-CC- (CH2)P- or -CH2-O-CH2- (wherein n is an integer of 2 to 3, and each of m and p is 0 or R2 is a :straight chain or branched alkyl group having 5 to 7 *c carbon atoms, -Ct H2t-OR3 (wherein t indicates an integer of 1 to 3, and R3 indicates a straight chain or branched alkyl group having 2 to 4 carbon atoms, or a phenyl group), -Ct H2t-CH=C (R4) (R 5 (wherein t indicates an integer of 1 to 3, and R4 and R5 each indicate hydrogen, a methyl group, an ethyl group, a propyl group or a butyl group); or -Ct H2t-C=C-R6 •(wherein t indicates an integer of 1 to 3, and R6 indicates hydrogen, a methyl group or an ethyl group).

Formula indicates 1- and dl-forms. In R2, -Ct H2t- represents a straight chain or branched alkylene group.

Of the above-described compounds, the following compound, beraprost, or a salt thereof is preferably used.

COOH

O

Ho

OH

The compounds represented by formula can be produced by, for example, the method disclosed in Japanese Examined Patent Publication No. 1-53672.

Oral or parenteral administration of the compounds represented by formula brings about the significant S. curative effect on cor pulmonale.

Cor pulmonale develops a cardiac disorder secondarily caused by various pulmonary diseases and pulmonary vascular diseases in the pathophysiological Sstate wherein hypoxemia (coexisting with hypercapnemia) resulting from pulmonary insufficiency continues, thereby causing right ventricular pressure overload (an increase in work load of the right ventricle). When this state continues, right ventricular hypertrophy and right ventricular failure arise. Cor pulmonale is classified into acute, subacute and chronic cor pulmonale. Although the compounds represented by formula of the present invention are effective -7against acute, subacute and chronic cor pulmonale, the compounds are particularly effective against chronic cor pulmonale.

A typical causal disease of acute cor pulmonale is pulmonary embolism which causes significant dilation of the right ventricle without right ventricular hypertrophy, resulting in right ventricular failure.

Although causes of subacute cor pulmonale include multiple and repetitive minor pulmonary embolism, dispersion of cancer to the lungs, and compression of 9*o the pulmonary main artery due to a tumor, etc., the condition thereof is similar to acute cor pulmonale.

"Chronic cor pulmonale is frequently caused by a chronic obstructive lung disease.

Examples of causal diseases of cor pulmonale include pulmonary embolism, dispersion of cancer to the lungs, pulmonary tuberculosis, compression of the *"pulmonary main artery due to a tumor, pulmonary infarction, diseases which cause primary disorder of the passage of air through the lungs and pulmonary alveoli (for example, chronic bronchitis, bronchial asthma, pulmonary emphysema, pulmonary fibrosis, pulmonary granulomatosis and humectation, pulmonary abscission, congenital pulmonary cyst, and height hypoxia), diseases causing primary disorder of the thoracic motion (for example, kyphyosis and other thoracic deformity, Hi__ iIi~ifLPG _XIi!IiiflFiii~ 1 pleural fibrosis, chronic nerve-muscular atrophy, obesity accompanied with alveolar hypoventilation, and cataplectic alveolar hypoventilation), diseases causing primary disorder of the pulmonary vessels (for example, primary disorder of the aterial paries, thrombotic diseases, embolism, mediastinal tumor, aneurysm, and compression of the pulmonary main artery and veins due to granulomatosis or fibrosis).

The agent for treating cor pulmonale of the present invention is used not only for treating cor pulmonale o but also for preventing cor pulmonale.

The compound represented by formula is S" administered to an adult one to three times a day in a dosage of 0.01 to 100 mg/person.

The agent for treating cor pulmonale of the.present invention may comprise at least one of the compounds represented by formula or salts thereof, or further *contain the additives below so that the agent in a solid state can orally be administered.

Examples of such additives include excipients such as starch, lactose, sucrose, grape sugar, mannitol, calcium carbonate, calcium sulfate, and the like; binders such as starch, dextrin, gum arabic, traganth, methyl cellulose, gelatin, polyvinyl pyrrolidone, polyvinyl alcohols and the like; disintegrators such as starch, polyvinyl pyrrolidone, crystalline cellulose and I~ the like; lubricants such as magnesium stearate, talc and the like; colorants; flavors; and the like.

The compounds represented by formula used in the present invention can be used in various conventional dosage forms such as tablets, sugar-coated tablets, powders. granules, troches, capsules, pills, syrup, and the like. The compounds may be paTenterally administered in the form of a sterilized solution, and other solutes such as sodium chloride or glucose in an amount sufficient to prepare an isotonic solution can also be used. Since the agent for treating cor pulmonale of the present invention has the stable S" chemical structure, it has no difficult in preparation and can be administered in the foregoing dosage forms for oral administration and a wide verity of other dosage forms such as an injection, a suppository, etc.

[EXAMPLE]

Although it will be described with reference to the following compound 1 beraprost sodium (referred to as "BPS" hereinafter) as an example that the compounds represented by formula have the effect of treating cor pulmonale, the compounds are not limited to this.

X_ (1) EXAMPLE 1 Model Test of Monocrotalin-Induced Disease: Monocrotalin was subcutaneously administered to 7week-old SD male rats, and, 7 days after the Sadministration, compound 1 was then continuously orally administered to the rats for 14 days to examine the effect of treating cor pulmonale. Compound 1 was used as a test compound. After the completion of the test, the rats were killed, and the weight ratio of the right ventricle of the heat, {weight of the right ventricle/(weight of the left ventricle weight of the septum) x was determined.

-11- BPS's action on weight ratio of right ventricle/[left ventricle+septum] of monocrotalin-administered rats mean S.E.M.

C C

U

C C

C

C.

0@ U

U

C S

S.

U

*UC S U. U *5 C S

C.

Normal 26.8 1.1 Control 50.0 2.9 BPS 0.01 mg/kg 42.9 2.7 BPS 0.03 mg/kg 36.1 2.6 BPS 0.1 mg/kg 38.9 3.3 Statistical significant difference: p<0.05, p<0.01 vs. control It was confirmed that compound 1 significantly depress an increase in the weight ratio of the right ventricle induced by monocrotalin, and thus has the effect of treating cor pulmonale.

EXAMPLE 2 Model Test of Interleukin-6-Induced Disease: Interleukin 6 was subcutaneously administered to 7week-old SD male rats for 6 days, and, 2 days after the administration, compound 1 was then continuously orally administered to the rats for 5 days to examine the effect of curing cor pulmonale. Compound 1 was used as a test compound. After the completion of the test, the rats were killed, and the weight ratio of the right ventricle of the heat, {weight of the right 99 .9 9 9 9* 9 p 9 9 9 9.

9. 9 99 9 9 *94 9 9999 9 9.

*9 9999 9 999999 9.

9* 9 *9 999*9* ventricle/(weight of the left ventricle weight of the septum) x was determined.

BPS's action on weight ratio of right ventricle/[left ventricle+septum] of IL-6-administered rats mean S.E.M.

Normal 26.1 0.9 Control 32.2 0.7 BPS 0.01 mg/kg 30.1 BPS 0.1 mg/kg 29.6 1.0 Statistical significant difference: p<0.05, p<0.01 vs. control It was confirmed that compound 1 significantly depress an increase in the weight ratio of the right ventricle induced by interleukin 6, and thus has the effect of treating cor pulmonale.

EXAMPLE 3 Pulmonary Embolism Model Test Collagen (5 gg/head) and epinephrine (0.6 gg/head) were simultaneously injected into the caudal veins of 7week-old ddY male mice (27-30g) obtained from Nippon S.L.C. Co., Ltd. to cause pulmonary embolism. One week after pulmonary embolism was induced, the wet weight/dry weight ratio of the lungs and the weight ratio of the right ventricle, {weight of the right ventricle/(weight -13-' of the left ventricle weight of the septum) x were determined. Compound 1 (0.01 mg/kg, 0.03 mg/kg, 0.1 mg/kg) was orally administered every day for 7 days from the day after inducing pulmonary embolism.

BPS's action on the wet weight/dry weight ratio of the lungs and the weight ratio of the right ventricle of pulmonary embolism model mice simultaneously administered with collagen and epinephrine *9 9 9 9 *999 99 99 9 *9 S 99 9 9 9 9 .9 9 Wet weight/dry weight ratio of lungs mean S.E.M.

Normal Control BPS 0.01 mg/kg BPS 0.03 mg/kg BPS 0.1 mg/kg 3.84 0.01 3.96 0.04 3.92 0.04 3.85 0.02 3.85 0.02 Weight ratio of right ventricle mean S.E.M.

28.2 0.9 32.3 0.9 30.1 1.4 27.8 1.4 27.3 1.1 Statistical significant difference: p<0.05, p<0.01 vs. control Compound 1 significantly depressed the wet weight/dry weight ratio of the lungs and exhibited the effect of inhibiting pulmonary embolism. Compound 1 further significantly depressed the weight ratio of the P:\OPER\MKR\SPEC\47320-96.273 30/9/99 -14right ventricle and was thus confirmed to have the effect of treating cor pulmonale.

INDUSTRIAL APPLICABILITY The agent of treating cor pulmonale of the present invention exhibits excellent pharmaceutical effects in both oral and parenteral administration.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.

*a 9

S

Claims

1. A method of treating cor pulmonale comprising administering to a cor pulmonale patient an effective amount of a 5,6,7-trinor-4,8-inter-m-phenyleneprostaglandin 12 derivative represented by the following formula A R, S R2 HO 20 wherein R, is hydrogen, a carboxyl group or a functional .derivative thereof, -CH20H, or a pharmacologically acceptable cation; A is (CH 2 -(CH2)-CH=CH- (CH2)p- (3) -(CH),-CEC-(CH2)p or -CH2-O-CH,- (wherein n is an integer of 0 to 3, and each of m and p is 0 or 1): R2 is a straight chain or branched alkyl group having to 10 carbon atoms, -Ct H2t-OR3 (wherein t indicates an integer of 1 to 5, and R3 indicates a straight chain or branched alkyl group having 1 to 5 carbon atoms, or a phenyl group), -Ct H2t-CH=C (R4) (Rs) (wherein t indicates the same as defined above, and R4 and R. each indicate hydrogen, a methyl group, an ethyl group, a propyl group or a butyl group); or -Ct H2t-C=C-R (wherein t indicates the same as defined above, and R6 indicates hydrogen, a methyl group or an ethyl group); wherein 35 ethyl group); wherein P:\OPER\MKR\SPECI\47320-96.273 30/9/99 S 4 I -16- formula indicates 1- and dl-forms; or a pharmacologically acceptable salt thereof.

2. A method according to Claim 1, wherein the compound represented by formula is beraprost or a pharmacologically acceptable salt thereof.

3. A method according to Claim 1, wherein cor pulmonale is acute, subacute or chronic cor pulmonale.

4. A method according to Claim 1, wherein cor pulmonale is chronic cor pulmonale. 0

5. A method of treating cor pulmonale substantially as 15 hereinbefore described with reference to the Example. DATED this 18th day of November 1999 20 Toray Industries, Inc. By DAVIES COLLISON CAVE Patent Attorneys for the Applicant