Composite Pharmaceutical Composition for Treatment of Fibrosis Disease

Abstract

The present disclosure relates to a composite composition of 2-methoxyestradiol and Chir99021 for the treatment of fibrosis. The composition according to the present disclosure inhibits collagen deposition and inflammatory response, and prevents the fibrosis of blood vessels and tissue damage, and thus has excellent preventive and therapeutic effects on fibrosis.

Claims

1. A pharmaceutical composition for the prevention or treatment of fibrosis, the pharmaceutical composition comprising 2-methoxyestradiol or a pharmaceutically acceptable salt thereof; and Chir99021 or a pharmaceutically acceptable salt thereof as an active ingredient.

2. The pharmaceutical composition of claim 1, wherein the fibrosis occurs from any one selected from the group consisting of lung, kidney, liver, heart, brain, blood vessels, joint, intestine, skin, soft tissue, bone marrow, penis, peritoneum, muscle, spine, testis, ovary, breast, thyroid gland, tympanic membrane, pancreas, gallbladder, bladder and prostate.

3. The pharmaceutical composition of claim 1, wherein the fibrosis is radiation-induced lung fibrosis.

4. The pharmaceutical composition of claim 1, wherein the fibrosis is idiopathic pulmonary fibrosis.

5. The pharmaceutical composition of claim 1, wherein the fibrosis is liver fibrosis.

6. The pharmaceutical composition of claim 3, wherein the radiation-induced lung fibrosis is accompanied by damage to blood vessels, tissue inflammation, or tissue fibrosis by radiation exposure.

7. The pharmaceutical composition of claim 5, wherein the liver fibrosis is nonalcoholic liver fibrosis.

8. The pharmaceutical composition of claim 1, wherein the composition is formulated for oral administration agents or injections.

9. A food composition for the prevention or improvement of fibrosis, the food composition comprising 2-methoxyestradiol or a food acceptable salt thereof; and Chir99021 or a food acceptable salt thereof as an active ingredient.

10. (canceled)

11. A method for the prevention or treatment of fibrosis, the method comprising administering a pharmaceutically effective dose of 2-methoxyestradiol or a pharmaceutically acceptable salt thereof; and Chir99021 or a pharmaceutically acceptable salt thereof to a subject in need thereof.

12. (canceled)

Description

DESCRIPTION OF DRAWINGS

[0060] FIG. 1 is a schematic diagram of the preparation of a radiation-induced lung fibrosis mouse model prepared by irradiating the chest of a mouse with radiation at an intensity of 4 mm and 90 Gy, and drug administration timing and dose.

[0061] FIG. 2 is a diagram showing results of confirming an inflammatory response and a degree of fibrosis at a tissue damage site according to drug administration in a radiation-induced lung fibrosis mouse model through hematoxylin and eosin staining.

[0062] FIG. 3 is a diagram statistically illustrating the degree of fibrosis according to drug administration in a radiation-induced lung fibrosis mouse model.

[0063] FIG. 4 is a schematic diagram of the preparation of a bleomycin-induced lung fibrosis mouse model and a drug administration timing.

[0064] FIG. 5 is a diagram illustrating results of confirming an inflammatory response and a degree of fibrosis at a tissue damage site according to drug administration in a bleomycin-induced lung fibrosis mouse model through hematoxylin and eosin staining.

[0065] FIG. 6 is a diagram illustrating results of confirming an inflammatory response and a degree of fibrosis at a tissue damage site according to drug administration in a bleomycin-induced lung fibrosis mouse model through trichrome staining.

[0066] FIG. 7 is a diagram statistically illustrating the degree of fibrosis according to drug administration in a bleomycin-induced lung fibrosis mouse model.

[0067] FIG. 8 is a schematic diagram of the preparation of a nonalcoholic liver fibrosis mouse model induced by intraperitoneal injection of CCl.sub.4 (1.5% CCl.sub.4:1 mg/kg) twice a week into the liver of a mouse, and drug administration timing and dose.

[0068] FIG. 9 is a diagram illustrating results of confirming a change in an inflammatory response and a degree of fibrosis at a tissue damage site according to drug administration in a nonalcoholic liver fibrosis mouse model through hematoxylin and eosin staining and trichrome staining.

[0069] FIG. 10 is a diagram statistically illustrating the degree of collagen deposition according to drug administration in a nonalcoholic liver fibrosis mouse model.

BEST MODES OF THE INVENTION

[0070] Hereinafter, the present disclosure will be described in more detail with reference to Examples. However, these Examples are only illustrative of the present disclosure, and the scope of the present disclosure is not limited to these Examples.

Example 1: Radiation-Induced Lung Fibrosis Inhibition Test According to Combined Administration of 2-Methoxyestradiol and Chir99021

[0071] Radiation was irradiated to the chest of a mouse at an intensity of 4 mm and 90 Gy to induce radiation-induced lung fibrosis. After irradiation, a drug was orally or not administered over a total of 6 times once every 2 days from the 4th day. For drug administration, 2-methoxyestradiol (2-Me) (30 mg/kg), Chir99021 (CHIR) (30 mg/kg), 2-Me+CHIR (30 mg/kg+30 mg/kg), Nintedanib (30 mg/kg), Pirfenidone (30 mg/kg) or Vehicle (non-administered) was administered to experimental animals. A solvent composition for drug administration was used under conditions of 5% DMSO, 30% PEG, and 1% Tween 80, and for Chir99021, a composition of 5% DMSO and 30% PEG was used.

[0072] On day 21 after irradiation, the experimental animals were sacrificed and autopsied to confirm specifically whether lung fibrosis was alleviated. A schematic diagram of the experimental process was shown in FIG. 1.

[0073] H&E staining was used to confirm an inflammatory response and fibrosis of a tissue damage site in a radiation-induced lung fibrosis mouse model. After fixing lung tissue with 10% formalin, paraffin sections were made and stained with hematoxylin and eosin. Specifically, the slid mouse tissue first reacted with xylene 3 times for 5 minutes each as a process of removing paraffin penetrated into the tissue, reacted with 100% ethanol twice, reacted with 95%, 70%, and 50% ethanol solutions for 3 minutes, respectively, and was washed with running water for 10 minutes after the 50% ethanol process was completed. The mouse tissue reacted with a hematoxylin solution for 2 minutes to stain a nucleus and was washed with running water for 10 minutes. Then, the mouse tissue reacted with an eosin solution for 30 seconds to stain a cytoplasm, reacted with 50%, 70%, 95%, and 100% ethanol processes for 1 minute, respectively, and finally reacted with a xylene solution, and then was added with a drop of mounting solution, and then covered with a cover slide and observed under a microscope.

[0074] In addition, using a trichrome staining method, fibrosis grades for living tissue were measured according to the following measurement standards.

TABLE-US-00001 Score Histological features 0 Normal lung 1 Minimal fibrous thickening of alveolar or bronchiolar walls 2 Moderate thickening of walls without obvious damage to lung 3 architecture 4 Increased fibrosis with definite damage to lung structure and 5 formation of fibrous bands or smallfibrous masses 6 Severe distortion of structure and large fibrous areas 7 8 Total fibrous obliteration of the field

[0075] Through hematoxylin and eosin staining, the cell nucleus may be observed in blue and the cytoplasm may be observed in pink.

[0076] The analyzed results were illustrated in FIGS. 2 and 3, respectively.

[0077] As can be seen in FIG. 2, it was found that tissue damage appeared in a non-administered group (Vehicle) after irradiation through hematoxylin and eosin staining. On the other hand, the treatment of 2-Me+CHIR significantly improved the degree of tissue damage, which exhibited a more excellent effect than not only 2-methoxyestradiol alone and Chir99021 alone, but also Nintedanib (30 mg/kg) and Pirfenidone (30 mg/kg) as positive controls.

[0078] In addition, as shown in FIG. 3, as a result of statistically confirming the degree of fibrosis and the degree of collagen deposition, considering the grade of fibrosis and the degree of collagen deposition, the treatment of 2-Me+CHIR greatly improved the lung fibrosis through a synergistic effect according to a combination thereof.

Example 2: Bleomycin-Induced Lung Fibrosis Inhibition Test According to Combined Administration of 2-Methoxyestradiol and Chir99021

[0079] 1.25 U/kg of bleomycin was injected into the respiratory tract of a mouse to induce bleomycin-induced lung fibrosis. After injection of bleomycin, a drug was intraperitoneally or not administered over a total of 7 times from the 7th day. For drug administration, 2-methoxyestradiol (2-Me) (60 mg/kg), Chir99021 (CHIR) (30 mg/kg), and 2-Me+CHIR (60 mg/kg+30 mg/kg) were administered to experimental animals or not administered thereto. A solvent composition for drug administration was used under conditions of 5% DMSO, 30% PEG, and 1% Tween 80, and for Chir99021, a composition of 5% DMSO and 30% PEG was used.

[0080] On day 21 after bleomycin injection, the experimental animals were sacrificed and autopsied to confirm specifically whether lung fibrosis was alleviated. A schematic diagram of the experimental process was shown in FIG. 4.

[0081] H&E staining was used to confirm an inflammatory response and fibrosis of a tissue damage site in a bleomycin-induced lung fibrosis mouse model. After fixing lung tissue with 10% formalin, paraffin sections were made and stained with hematoxylin and eosin. Specifically, the slid mouse tissue first reacted with xylene 3 times for 5 minutes each as a process of removing paraffin penetrating into the tissue, reacted with 100% ethanol twice, reacted with 95%, 70%, and 50% ethanol solutions for 3 minutes, respectively, and was washed with running water for 10 minutes after the 50% ethanol process was completed. The mouse tissue reacted with a hematoxylin solution for 2 minutes to stain a nucleus and was washed with running water for 10 minutes. Then, the mouse tissue reacted with an eosin solution for 30 seconds to stain a cytoplasm, reacted with 50%, 70%, 95%, and 100% ethanol processes for 1 minute, respectively, and finally reacted with a xylene solution, and then was added with a drop of mounting solution, and then covered with a cover slide and observed under a microscope. Through hematoxylin and eosin staining, the cell nucleus may be observed in blue and the cytoplasm may be observed in pink.

[0082] In addition, using a trichrome staining method, fibrosis grades for living tissue were measured. In the case of trichrome staining, the mouse tissue was fixed with 10% formalin for 5 days and a paraffin block was made. In order to remove paraffin in the tissue, the mouse tissue reacted with xylene 3 times for 5 minutes each, and reacted with 100%, 95%, 75%, and 50% ethanol solutions for 3 minutes, respectively, and was washed with running water for 10 minutes after the last reaction was completed. First, the mouse tissue reacted with a Bouin's solution in a water bath at 60° C. for 1 hour. After the reaction, the mouse tissue was washed in running water for 10 minutes, mixed with Weigert's hematoxylins A and B at a 1:1 ratio, reacted for 10 minutes, and then was washed in running water for 10 minutes. Then, the mouse tissue reacted with red staining for 3 minutes and was rinsed once with tertiary distilled water, and then reacted with phosphhotunstic/phosphomolydic acid for 20 minutes and aniline blue for 30 minutes, rinsed 3 times with tertiary distilled water, and then sequentially reacted with 1% acetic acid for 1 minute. Finally, after the dehydration process and the xylene solution were finished, a drop of mounting solution was dropped, and then covered with a cover glass, and observed under a microscope. Collagen deposition may be observed in blue through trichrome staining.

[0083] The analyzed results were illustrated in FIGS. 5, 6, and 7.

[0084] As can be seen in FIG. 5, it was found that tissue damage appeared in a non-administered group (Bleomycin) after bleomycin injection through hematoxylin and eosin staining. On the other hand, the treatment of 2-Me+CHIR(Bleomycin+2-Me+CHIR) significantly improved the degree of tissue damage, which exhibited a more excellent effect than treatment of 2-methoxyestradiol alone and Chir99021 alone, respectively.

[0085] In addition, as illustrated in FIG. 6, it was found that tissue damage and collagen deposition were shown in the non-administered group (Bleomycin) after administration of bleomycin through trichrome staining. On the other hand, the administration of 2-methoxyestradiol (2-ME) and Chir99021 (CHIR) significantly improved the tissue damage and collagen deposition.

[0086] Specifically, as shown in FIG. 7, as a result of statistically confirming the degree of fibrosis and the degree of collagen deposition, considering the grade of fibrosis and the degree of collagen deposition, the treatment of 2-Me+CHIR greatly improved the lung fibrosis through a synergistic effect according to a combination thereof.

Example 3. Nonalcoholic Liver Fibrosis Inhibition Test According to Combined Administration of 2-Methoxyestradiol and Chir99021

[0087] Nonalcoholic liver fibrosis was induced by intraperitoneal injection of CCl.sub.4 (1.5% CCl.sub.4:1 mg/kg) twice a week into the liver of a mouse. After 4 weeks of CCl.sub.4 administration, 2-methoxyestradiol (2-ME) and Chir99021 (CHIR) (30 mg/kg+30 mg/kg), obeticholic acid (OBC) (10 mg/kg), 2-ME (30 mg/kg) or vehicle (non-administered) was administered, and then liver tissue damage and fibrosis were observed after 6 weeks.

[0088] The schematic diagram thereof was illustrated in FIG. 8.

[0089] In order to confirm the inflammatory response and fibrosis of a tissue damage site in a nonalcoholic liver fibrosis mouse model, hematoxylin and Eosin staining and trichrome staining were used similarly to Examples 1 and 2. After fixing liver tissue with 10% formalin, paraffin sections were made and stained with hematoxylin and eosin and trichrome. Through hematoxylin and eosin staining, the cell nucleus may be observed in blue and the cytoplasm may be observed in pink, and through trichrome staining, the collagen deposition may be observed in blue.

[0090] The results thereof were illustrated in FIGS. 9 and 10.

[0091] As can be seen in FIG. 9, it could be seen that tissue damage and collagen deposition were shown in a non-administered group (Vehicle) after irradiation through hematoxylin and eosin staining and trichrome staining.

[0092] On the other hand, the administration of 2-methoxyestradiol (2-ME) and Chir99021 (CHIR) significantly improved the tissue damage and collagen deposition.

[0093] In particular, as can be seen in FIG. 10, administration of 2-methoxyestradiol (2-ME) and Chir99021 (CHIR) significantly improved collagen deposition. Furthermore, the combined administration of 2-methoxyestradiol (2-ME) and Chir99021 (CHIR) greatly inhibited the tissue damage and the collagen deposition through a synergic effect to greatly improve fibrosis of liver tissue.

[0094] When combining the results, the combined administration of 2-methoxyestradiol and Chir99021 inhibits the collagen deposition in fibrosis, inhibits the inflammatory response, prevents the fibrosis of blood vessels and prevents the tissue damage, thereby exhibiting an excellent effect on fibrosis. In particular, the combination of these two compounds greatly improved the symptoms of fibrosis through a synergistic effect.

[0095] In addition, through animal experiments, it was confirmed that administration of 2-methoxyestradiol and Chir99021 had excellent preventive and therapeutic effects on fibrosis by inhibiting radiation-induced lung fibrosis in vivo, drug (such as bleomycin)-induced lung fibrosis, and nonalcoholic liver fibrosis.

[0096] Accordingly, the 2-methoxyestradiol or the pharmaceutically acceptable salt thereof; and the Chir99021 or the pharmaceutically acceptable salt thereof may be very usefully used for preventing or treating fibrosis.

[0097] It will be appreciated by those skilled in the art that the present disclosure as described above may be implemented into other specific forms without departing from the technical spirit thereof or essential characteristics. Thus, it is to be appreciated that embodiments described above are intended to be illustrative in every sense, and not restrictive. The scope of the present disclosure is represented by claims to be described below rather than the detailed description, and it is to be interpreted that the meaning and scope of the claims and all the changes or modified forms derived from the equivalents thereof come within the scope of the present disclosure.