Internally administered therapeutic agents for cranial nerve diseases comprising mesenchymal cells as an active ingredient

a technology of mesenchymal cells and therapeutic agents, which is applied in the direction of drug compositions, extracellular fluid disorders, instruments, etc., can solve the problems of difficult preparation of neural stem cells from patients or other persons, difficult collection of tissues containing neural stem cells from the cerebrum, and complicated technique, etc., to prevent endothelial cells from ischemic damage, stimulate angiogenesis, and facilitate and safe obtained

Inactive Publication Date: 2006-09-21
NC MEDICAL RES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0162] The mechanisms of therapeutic benefits of MSCs transplantation for stroke, may result from neuroprotection and angiogenesis. A number of neurotrophic factors have been reported to have therapeutic effects on cerebral infarction. These include BDNF, GDNF, NGF, EGF, and bFGF. Mechanisms proposed for the neuroprotective effect of these agents include anti-apoptotic activity, free radical scavenging, anti-inflammatory activity, and anti-glutamate excitotoxicity.
[0163] An advantage of PMSCs for transplantation studies is that they can be easily and safely obtained in large numbers from blood, which is a less invasive proceed than extracting from bone marrow.
[0164] MSCs also provide several angiogenic growth factors such as VEGF and bFGF, which may prevent endothelial cells from ischemic damage or stimulate angiogenesis. These cells produce soluble mediators that down-regulate immune responses which could also contribute to neuroprotection. Hemodynamic changes of cerebral blood flow after MCAO with and without MSCs transplantation were analyzed by PWI. While both control and MSCs transplantation groups showed improvement of rCBF in the lesi

Problems solved by technology

It is not impossible to prepare such cells from patients or other persons for use in cell therapy; however, it is problematic since tissue material must be collected from either the brain or nerves.
However, although it doesn't cause symptoms of neurological deficiency, collecting tissues that contain neural stem cells from the cerebrum is

Method used

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  • Internally administered therapeutic agents for cranial nerve diseases comprising mesenchymal cells as an active ingredient
  • Internally administered therapeutic agents for cranial nerve diseases comprising mesenchymal cells as an active ingredient
  • Internally administered therapeutic agents for cranial nerve diseases comprising mesenchymal cells as an active ingredient

Examples

Experimental program
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Effect test

example 1

[0241] [Example 1] Transient middle cerebral artery occlusion model A rat middle cerebral artery occlusion model was used as a stroke model. Transient middle cerebral artery occlusion (MCAO) was induced for 45 minutes using the intravascular occlusion method (E.Z. Longa, P.R. Weinstein, S. Carlson, R. Cummins, Reversible middle cerebral artery occlusion without craniectomy in rats, Stroke 20 (1989) 84-91).

[0242] Adult male Sprague-Dawley rats (n=1 13) weighing 250 to 300 g were anaesthetized with 5% isoflurane, and the anesthesia was mechanically maintained with 1.5% isoflurane in a gaseous mixture of 70% N20 and 30% O2 under artificial ventilation. The rectal temperature was maintained at 37° C. using an infrared heat lamp. A cannula was inserted into the left femoral artery during surgery, for measuring blood pH, P02, and pCO2. The tip of a 20.0 to 22.0 mm long 3-0 surgical suture (Dermalon: Sherwood Davis & Geck, UK) was rounded by heating near a flame, and was advanced from the ...

example 2

[0244] [Example 2] Preparation of bone marrow cells

[0245] Autologous bone marrow was collected from the femur of MCAO rats, one and a half hours prior to bone marrow cell transplant.

[0246] The rats were anaesthetized with ketamine (75 mg / kg) and xylazine (10 mg / kg; i.p.). A 1 cm incision was made in the skin, a small hole (2x 3 mm) was punctured in the femur using an air drill, and 1 ml of bone marrow was aspirated using a 22-gauge needle. The collected samples were diluted and suspended in a medium containing 2 ml of L- 15 medium and 3 ml of Ficoll (Amersham Biosciences). After centrifugation at 2,000 rpm for 15 minutes, mononuclear cell fractions were collected and resuspended in 2 ml serum-free medium (NPMM: Neural Progenitor Cell Maintenance Medium; Clonetics, San Diego, CA, USA). Following a second centrifugation (2,000 rpm, 15 minutes), cells were suspended in 1 ml of NPMM.

example 3

[0247] [Example 3] Experimental groups

[0248] The experiment was conducted using 11 groups (n=88). Nothing was administered to the Group 1 (control) rats after MCAO (n=8). The rats in Groups 2 to 6 were intravenously administered with just the medium (without donor cell administration), 3, 6, 12, 24, and 72 hours after MCAO (n=8 for each group). The rats in Groups 7 to 11 were intravenously administered with the autologous bone marrow cells (1.0×107 cells), 3, 6, 12, 24, and 72 hours after MCAO (each group n=8). Six rats in each group were used to calculate the infarct volume, and the others were used for other histological analyses.

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Abstract

Intravenous administration of bone marrow cells collected from rat bone marrow or peripheral blood to a rat cerebral infarction model was found to be effective in treating cerebral infarction. Human and murine bone marrow stem cells showed similar effects. Mesenchymal cells such as bone marrow cells, cord blood cells, or peripheral blood cells can be used as agents for in vivo administration against cranial nerve diseases.

Description

[0001] This application is a continuation-in-part of Application Ser. No. 10 / 562,202, which is a national phase application of PCT / JP04 / 009386 filed on Jun. 25, 2004. The entire of contents of Application No. 10 / 562,202, include the specification, drawing, claims, sequence listing and abstract are hereby incorporated by reference.TECHNICAL FIELD [0002] The present invention relates to cranial nerve disease therapeutic agents for in vivo administration, which comprise mesenchymal cells, particularly bone marrow cells, cord blood cells, or peripheral blood cells, or cells derived from these cells as active ingredients. BACKGROUND ART [0003] In recent years regenerative medical techniques have been in the limelight. In regenerative medical techniques, disorders that the natural, inherent regenerative-healing ability of the human body cannot cure can be cured by regenerating organs and such using artificial proliferation of autologous cells, and then surgically conjugating these at the ...

Claims

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Application Information

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IPC IPC(8): A61K48/00C12N5/08A61K35/12A61K35/28
CPCA61K35/28A61K2035/124G01N2800/285G01N2800/2871A61P7/00
Inventor HONMOU, OSAMUHAMADA, HIROFUMI
Owner NC MEDICAL RES
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