Use of Vinca Alkaloids and Salts Thereof

a technology of vinca alkaloids and salts, which is applied in the field of use of vinca alkaloids and their salts, can solve the problems of increased blood glucose concentration, increased neuropathy, laborious four injections a day for patients, etc., and achieves the effect of increasing insulin production and increasing insulin-producing and secreting abilities

Inactive Publication Date: 2007-10-04
KEIO UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0038] Activin, which is capable of inducing AR42J cells to produce insulin, does not exhibit the effect on porcine pancreatic cells. To induce ES cells to produce insulin, many factors including leukocyte activating factor (LAF) as well as many processes are required. The conditions under which cells are induced to differentiate are different depending on the individual cell type. For this reason, even those skilled in the art could not predict that a vinca alkaloid increases insulin production of non-neoplastic cells...

Problems solved by technology

Diabetes is a disease arising from shortage of blood insulin and impaired insulin function, resulting in increased blood glucose concentrations, accompanied by complications such as neuropathy, visual disturbance, renal damage, etc.
It is needless to say that, in such cases, four injections a day are laborious to patients.
However, the inhibitor is not very effective and causes obesity as a side effect, as has been pointed out.
In other cases, agents such as sulfonylurea, which promotes insulin release from β cells, are used, but they are also not very effective.
The technique for collecting large amounts of cells and inducing them to differentiate into insulin producing and ...

Method used

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  • Use of Vinca Alkaloids and Salts Thereof
  • Use of Vinca Alkaloids and Salts Thereof
  • Use of Vinca Alkaloids and Salts Thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

Production Example 1

Preparation of Conophylline

[0091] Conophylline was isolated and purified from leaves of Ervatamia microphylla, an Apocynaceae family plant, (harvested in Khon Khen, Thailand) in the following manner.

[0092] Active substance was extracted from about 4 kg of Ervatamia micorophylla leaves with 100 L of chloroform to afford about 130 g of oily substance. This oily substance was chromatographed on a silica gel column (purification was performed by a total of 5 rounds of column chromatography using about 500 g of silica gel), eluting sequentially with chloroform:methanol (40:1 and 20:1). Subsequently, using morphological changes of K-ras-NRK cells as an activity marker, the fractions exhibiting this biological activity were recovered. The crude purified product obtained (about 40 g) was chromatographed on a silica gel column with n-hexane:ethyl acetate (1:2 and 0:1) (using about 500 g of silica gel; purchased from Merck Co.) to afford 1.5 g of active fractions. The a...

example 2

Experimental Examples I and II

1. Methods

[0093] Neonatal pigs within 72 hours of birth were obtained from the (Takayama) pig farm. The whole pancreas (ventral and dorsal pancreas) was removed under general anesthesia immediately after animals were brought to the operating room. After elimination of connective tissue covering the removed pancreas and blood adhering to it, the pancreas was transferred to a 10 ml beaker and dissected into small pieces with ophthalmic scissors. The dissected pieces were transferred to a 100 ml conical flask, to which 50 to 60 ml of phosphate buffered saline (PBS) was added. After a 3 min rotation at 110 rpm on a low speed stirrer, the mixture was allowed to stand still and the supernatant was discarded. Then, 40 mL of phosphate buffered saline containing Liberase PI (Roche) at a concentration of 2.5 mg / ml was added. After an 8 min rotation at 110 rpm on a low speed stirrer, the mixture was allowed to stand still and the supernatant containing the cell...

example 3

Comparative Example 1

Effect in Which Conophylline Induces Differentiation of Rat Pancreatic Acinar Carcinoma AR42 J-B13 Cells Into Insulin-Producing Cells

1. Methods

Cell Culture

[0108] DMEM was sterilized by filtration after its pH was adjusted to 7.4 in the presence of 20 mM HEPES-NaOH. AR42J-B13 cells (endowed by Dr. Itaru Kojima, Institute for Cellular and Molecular Regulation, Gunma University) a highly sensitive subclone of AR42J, were cultured at 37° C. in a 5% CO2 incubator with 20 ml of culture medium DMEM supplemented with 100 mg / l kanamycin, 0.6 g / l glutamine, 100 unit / ml penicillin G, 5 mM NaHCO3, and 10% FBS. To prevent transformation due to a high density of the cells and to retain differentiation ability of the cells, the cells were transferred every 2 to 3 days to maintain 2.5% to 5% of confluency. The cell transfer was performed as follows: After the medium was removed, the cells were washed twice in PBS− (Ca2+, Mg2+-free PBS; 8 g / l, NaCl, 0.2 g / l KCl, 0.916 g / Na...

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Abstract

An agent containing a vinca alkaloid or its pharmacologically acceptable salt as an active ingredient can induce insulin production and/or secretion of non-neoplastic cells derived from the pancreas.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] This application claims the benefit of priority to Japanese Patent Application No. 2003-13125, filed on May 9, 2003 and Japanese Patent Application No. 2003-373665, filed on Oct. 31, 2003, both of which are incorporated herein by reference. TECHNICAL FIELD [0002] The present invention relates to the use of vinca alkaloids and their salts. More specifically, the present invention relates to agents that enhance insulin-producing and / or -secreting abilities of non-neoplastic cells derived from the pancreas, therapeutic agents for diabetes, blood glucose level-lowering agents, methods for inducing differentiation of non-neoplastic cells derived from the pancreas, methods for enhancing insulin-producing and / or -secreting abilities of non-neoplastic cells derived from the pancreas, methods for producing pancreas-derived non-neoplastic cells whose insulin-producing ability has been enhanced, methods for culturing non-neoplastic cells derived f...

Claims

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Application Information

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IPC IPC(8): A61K38/18A61K31/4745A61K31/455A61P3/10C07D491/22C12N5/07C12N5/071C12N5/079C12N5/09
CPCC07D491/22A61K31/455A61P13/12A61P25/00A61P27/02A61P3/10A61P43/00A61P9/10
Inventor UMEZAWA, KAZUOOHGAWARA, HISAKOKOJIMA, ITARUKOYANO, TAKASHI
Owner KEIO UNIV
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