IP Library Granted Patent US 9,596,834
Granted Patent B2
US 9,596,834 · App. 14/191,942 · Granted Mar 21, 2017

Steatohepatitis-liver cancer model animal

Inventors: Hiroyuki Yoneyama (Tokyo, JP); Masato Fujii (Tokyo, JP)
Assignee: Stelic Institute of Regenerative Medicine, Stelic Institute & Co.
A01K67/027A01K2207/20A01K2207/25A01K2227/10A01K2267/0331
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Quick Facts
Patent No.
US 9,596,834
App. No.
14/191,942
Granted
Mar 21, 2017
Kind
B2
Abstract

Fatty liver was induced by administering agents for inducing organ inflammation to experimental animals to evoke insulin resistance and by rearing them with high-fat diets. As a result, steatohepatitis was successfully induced in the animals. The animals show pathological findings similar to those of humans. By using these model animals, substances for treating or preventing diseases can be efficiently screened and the efficacy of medicinal substances can be effectively evaluated.

Claims (17)

1. A non-human animal model, which is produced by:

(a) administering to a non-human mammal of one to five days old an N-acetyl-β-D-glucosaminidase inhibitor in an amount sufficient to induce organ inflammation wherein the inhibitor is selected from the group consisting of streptozotocin and Pugnac;

(b) rearing the mammal with a high-fat diet over a period of time sufficient to induce liver cirrhosis; and

(c) further rearing the mammal with a high-fat diet over a period of time sufficient to induce liver cancer caused by cirrhosis, developed such that it displaces normal liver cells of the mammal.

2. The non-human animal model of claim 1 , wherein the non-human mammal is a mouse.

3. The non-human animal model of claim 1 , wherein, in step (a), the mammal is two days old.

4. The non-human animal model of claim 1 , wherein the ratio of fat-derived calories to total calories of the high-fat diet is 50% or more.

5. A non-human animal model, which is produced by:

(a) administering to a non-human mammal of one to five days old an N-acetyl-β-D-glucosaminidase (O-GlcNAcase) inhibitor in an amount sufficient to induce organ inflammation wherein the inhibitor is a nucleic acid sequence suppressing expression of an O-GlcNAcase gene;

(b) rearing the mammal-with a high-fat diet over a period of time sufficient to induce liver cirrhosis; and

(c) further rearing the mammal with a high-fat diet over a period of time sufficient to induce liver cancer caused by cirrhosis, developed such that it displaces normal liver cells of the mammal.

6. The non-human animal model of claim 5 , wherein the non-human mammal is a mouse.

7. The non-human animal model of claim 5 , wherein, step (a), the mammal is two days old.

8. The non-human animal model of claim 5 , wherein the ratio of fat-derived calories to total calories of the high-fat diet is 50% or more.

9. The non-human animal model of claim 5 , wherein the nucleic acid sequence is an siRNA sequence.

10. The non-human animal model of claim 5 , wherein the nucleic acid sequence is an antisense sequence.

11. The non-human animal model of claim 5 , wherein the nucleic acid sequence is a ribozyme that targets an O-GlcNAcase gene.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded Mar 12, 2020
From: SMC ASSET, INC.; SMC PARTNERS, INC.; SMC GLOBAL ASSET, INC.
To: SMC GLOBAL ASSET, INC.
Reel/Frame 052159/0170 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2017
From: STELIC INSTITUTE OF REGENERATIVE MEDICINE, STELIC INSTITUTE & CO.
To: SMC ASSET, INC.
Reel/Frame 041460/0284 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2014
From: YONEYAMA, HIROYUKI; FUJII, MASATO
To: STELIC INSTITUTE OF REGENERATIVE MEDICINE, STELIC INSTITUTE & CO.
Reel/Frame 032757/0995 →
Continuity (2)
Continuation 13319851
Related Publication 20140178306A1 · Jun 26, 2014