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Methods for treating disorders using plant extracts

a technology of plant extracts and disorders, applied in the field of materials and methods for treating disorders using plants, can solve the problems of secondary health problems that require additional medical treatment, inability to control blood glucose levels, and insufficient indicators, so as to improve the activity of insulin receptor agonists, and improve the effect of hyperglycemia

Inactive Publication Date: 2005-03-31
RIBNICKY DAVID M +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

"The present invention provides a convenient method for obtaining extracts from plants such as Artemisia and using them to modulate blood glucose levels and GLP-1 activity in mammals. The extracts can be used to control blood glucose levels, promote weight gain, and treat Type 2 diabetes. The invention also provides a method for reducing insulin resistance and a pharmaceutical composition containing the extracts. The extracts can be administered through various routes, including injection and oral. Overall, the invention provides a safe and effective way to manage blood glucose levels and treat diabetes."

Problems solved by technology

The disorder results from an inability to control blood glucose levels, for example due to insufficient levels or activity of insulin.
Elevated glucose levels, in turn, often lead to secondary health problems that require additional medical treatment.
While these health risks are associated with diabetes, they are not, by themselves, useful indicators of diabetes.
Drug therapy, however, does not always achieve satisfactory glycemic control and insulin use often promotes hypoglycemia.
Moreover, these conventional treatments often lower blood glucose by promoting the non-selective uptake of glucose by many cells, including adipocytes, which contributes to undesirable weight gain.
Additionally, traditional treatments, like insulin injections, are expensive and can be painful to administer.
The authors of this study did not, however, test for the presence of mutagens or toxins and did not explore the use of such extracts to treat disorders, diseases or conditions other than hyperlipidemia.
Extracts were never prepared from the tarragon.
PCT Publication WO 97 / 35598 describes aqueous (i.e., water) extracts of Artemisia judaica as having an insulinomimetic anti-diabetic effect, but also notes the presence of a deleterious mutagen that would render the crude extract unsuitable for administration to mammals such as humans.
Therefore, not all Artemisia plants, e.g., not A. judaica, appear suitable for use in extracts for treating mammals having a disorder such as diabetes.

Method used

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  • Methods for treating disorders using plant extracts
  • Methods for treating disorders using plant extracts
  • Methods for treating disorders using plant extracts

Examples

Experimental program
Comparison scheme
Effect test

example 1

Extract Preparation

Artemisia dracunculus seeds (Richters Seeds) were germinated in a 0.9 cm deep well inside Grodan rock wool cubes (3.4 cm width×3.4 cm depth×3.7 cm height). One week later the seedlings were placed into a hydroponic system with a nutrient solution (120 g Hydro-Sol [Scotts-Sierra Horticultural Products Comp., Marysville, Ohio, USA] supplemented with 5 g NH4NO3 and 90 g Ca(NO3)2 in 60 liters of water). Aeration was provided by bubbling compressed air through the hydroponic nutrient solution at a flow rate of about 100 ml per minute for deep hydroponics (i.e., continuous immersion in water deeper than 4 cm). Alternatively, the seedlings were placed into a shallow gutter hydroponic system with a continuous flow of nutrient solution. The plants were elicited with 0.1% chitosan in the hydroponic solution 24 hours prior to harvest. The use of chitosan for elicitation of the plants provided greater hypoglycemic (i.e., blood glucose lowering) activity than untreated plant...

example 2

Efficacy of Alcoholic Extract of Artemisia dracunculus

The efficacy of the Artemisia dracunculus extract was evaluated in Streptozotocin (STZ)-treated mice. STZ induces diabetes by destroying most, if not all, of the beta cells of the pancreas, leaving the animals with little or no insulin production and severe hyperglycemia [Hisashi, et al., European Journal of Pharmacology, 87:237-243 (1983)]. This is a stringent assay for anti-diabetic efficacy, in which many of the currently prescribed drugs do not show significant activity. Mice were treated with STZ as described by Hisashi et al., European Journal of Pharmacology, 87:237-243 (1983). A 500 mg / kg dose of Artemisia dracunculus extract was administered daily by oral gavage to STZ-treated mice for a period of 7 days. Additionally, a dose of insulin (1 IU / kg) was administered subcutaneously to STZ-treated mice, while 20 ml / kg of vehicle only (0.9% NaCl or 2% Tween 80 in distilled water) was administered to STZ-treated mice, as a co...

example 3

Hypoglycemic Activity of Alcoholic Extract on Non-Diabetic Mice

The possible hypoglycemic activity of Artemisia dracunculus extracts was investigated in non-diabetic mice. The mice were exposed to Artemisia dracunculus extracts prepared as described in Example 1, which were administered orally to the mice in the form of a coating on their food. To obtain reliable data, control mice were provided with vehicle-coated food. The vehicle was 0.9% NaCl or 2% Tween 80 in distilled water. The feeding regimen was continued for seven days, and insulin and blood glucose levels were then determined using a technique well known in the art. (ELISA Insulin Assay kit (SPI bio, France); Glucose-HA Assay kit (Wako, Japan)). Mice fed vehicle (10 ml / kg) served as the control. Artemisia dracunculus extracts, at a dosage level of 500 mg / kg, caused statistically insignificant reductions in the blood glucose concentrations of non-diabetic animals; the changes in insulin concentrations of the extract-fed m...

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PUM

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Abstract

The present invention provides materials and methods relating to mildly polar fluid extracts of plant materials, such as Artemisia plant species, useful in methods for treating diabetes and methods for modulating the activity of glucagon-like peptide-1 (GLP-1), and in methods for modulating phosphoenol pyruvate carboxykinase (PEPCK) activity in a diabetes-specific manner. The extracts are generally non-toxic and non-mutagenic and may be administered to diabetics with beneficial effect on blood glucose levels. The extracts may also be administered to non-diabetics without deleterious effect. The plants are easily grown with a minimum of time, labor, and cost. Extracts are inexpensively and quickly prepared without the need for fractionation to remove potentially deleterious compounds, and the extracts may be administered to mammals such as humans through various routes, in a variety of forms, and at convenient concentrations.

Description

FIELD OF INVENTION The present invention relates to materials and methods for treating a disorder using plants. More specifically, the invention relates to materials and methods for treating a disorder using extracts of the plant genus Artemisia. BACKGROUND Diabetes is a major health concern, as evidenced by the number of people it affects as well as the costs incurred in treating or preventing it. According to the American Diabetes Association, there are 15.7 million people, or 5.9% of the U.S. population, that suffer from diabetes. Only about 10.3 million of these people have been diagnosed with the disease. With approximately 5.4 million people unaware that they have this chronic condition, diabetes ranks as the seventh leading cause of death in the U.S. The costs associated with efforts to treat and / or to prevent the condition are commensurate with the number of people afflicted, both in the U.S. and throughout the world. Diabetes is a complex condition or disease that is mos...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K36/282A61K36/28A61K45/06A61P3/00A61P3/10A61P9/10A61P9/12A61P13/12A61P15/10A61P25/00A61P25/28A61P27/02A61P27/12A61P31/04A61P43/00
CPCA61K36/282A61K45/06A61K2300/00A61P13/12A61P15/10A61P21/00A61P25/00A61P25/28A61P27/02A61P27/12A61P3/00A61P3/02A61P3/04A61P31/04A61P3/08A61P43/00A61P9/10A61P9/12A61P3/10
Inventor RIBNICKY, DAVID M.RASKIN, ILYA
Owner RIBNICKY DAVID M
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