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Application of NMN combined CD38 inhibitor in preparation of medicine for preventing or treating cardiotoxicity caused by adriamycin

A technology of CD38 and cardiotoxicity, applied in the field of biomedicine, can solve the problems of no significant increase in tissue NAD level, low NAD replenishment efficiency, and weakened NAD effect, so as to relieve the limitations of clinical application, increase cardiac NAD content, and weaken DIC. Effect

Pending Publication Date: 2021-12-07
ZHONGSHAN HOSPITAL FUDAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, recent clinical studies have found that supplementing NMN in the human body does not significantly increase the level of NAD in tissues. The low efficiency of NAD supplementation greatly weakens the role of NAD in preventing and treating diseases, thus limiting its wide clinical application

Method used

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  • Application of NMN combined CD38 inhibitor in preparation of medicine for preventing or treating cardiotoxicity caused by adriamycin
  • Application of NMN combined CD38 inhibitor in preparation of medicine for preventing or treating cardiotoxicity caused by adriamycin
  • Application of NMN combined CD38 inhibitor in preparation of medicine for preventing or treating cardiotoxicity caused by adriamycin

Examples

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Embodiment 1

[0021] as per figure 1 The technical route shown is to construct an animal model of doxorubicin cardiotoxicity, specifically: inject 5 mg / kg of doxorubicin or normal saline into the tail vein of 8-week-old C57BL / 6 male mice, and the administration frequency is once a week, For four consecutive weeks, the cumulative dose of doxorubicin was 20 mg / kg, and the end point of the DIC model was 4 weeks after the last administration. Drug combination application: NMN was dissolved in saline, and 78c was dissolved in DMSO. Three hours before doxorubicin injection, mice were injected intraperitoneally with 500 mg / kg NMN and 10 mg / kg CD38 inhibitor 78c. The frequency of NMN administration was once every two days and 78c was once a day until the end of the model. After the end of the model, echocardiography was performed on the mice to detect the heart function of the mice, and the myocardial tissue of the mice was taken to detect the NAD content. The results are as follows: figure 2 –4...

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Abstract

The invention belongs to the technical field of biological medicine, and discloses application of an NMN combined CD38 inhibitor in preparation of a medicine for preventing or treating cardiotoxicity caused by adriamycin, the dosage ratio of the NMN to the CD38 inhibitor is 0.1-100: 1, when the NMN combined CD38 inhibitor 78c and an anti-tumor medicine adriamycin are used in a combined mode, the NMN can effectively increase the NAD content of the heart, remarkably weaken DIC and improve the heart function, and the NMN and the CD38 inhibitor 78c are combined with the anti-tumor medicine adriamycin. Therefore, the limitation of adriamycin clinical application is relieved, and a basis is provided for new drug research and development and innovative therapy.

Description

technical field [0001] The invention belongs to the technical field of biomedicine, and specifically relates to the application of NMN combined with CD38 inhibitors in the preparation of drugs for preventing or treating cardiotoxicity caused by doxorubicin. Background technique [0002] Anthracyclines represented by doxorubicin (DOX) are an important class of chemotherapy drugs, which are widely used in the treatment of solid and hematological malignancies, such as breast cancer, acute leukemia, lymphoma, etc. However, doxorubicin-induced cardiotoxicity (DIC) severely limits its clinical application. Although the new liposomal doxorubicin has improved the targeting of tumors, the cardiotoxicity caused by it has not been completely eliminated. Once congestive heart failure caused by doxorubicin occurs, the lethal rate is as high as 50%. At present, there is no effective treatment for DIC. Dextropropanimine is the only drug approved by the FDA for the prevention of DIC. Howev...

Claims

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Application Information

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IPC IPC(8): A61K45/06A61K31/706A61K31/704A61P9/00
CPCA61K45/06A61K31/706A61K31/704A61P9/00A61K2300/00
Inventor 葛均波罗伟孙爱军张倍健董正翁鑫宇高婷雯蔡赟赵永超邹小乙
Owner ZHONGSHAN HOSPITAL FUDAN UNIV