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Peptide YY and Peptide YY Agonists for Treatment of Metabolic Disorders

a metabolic disorder and agonist technology, applied in the field of peptide yy and peptide yy agonists for the treatment of metabolic disorders, can solve the problems of reducing life span, carries a serious risk of co-morbidities, and obesity and its associated disorders are common and serious public health problems, so as to reduce nutrient availability and modulate nutrient availability

Inactive Publication Date: 2013-01-24
ASTRAZENECA PHARMA LP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0013]It has been discovered that, contrary to reported activities of central administration of members of the pancreatic polypeptide family, peripheral administration of PYY and PYY agonists reduces nutrient availability and is useful in the treatment of obesity and related disorders. PYY and PYY agonist compositions and uses thereof are disclosed herein to modulate nutrient availability in a patient for treating metabolic disorders which may be benefited by a reduction in nutrient availability. These methods will be useful in the treatment of, for example, obesity, diabetes, including but not limited to type 2 or non-insulin dependent diabetes, eating disorders, insulin-resistance syndrome, and cardiovascular disease.
[0016]One such PYY agonist analog is PYY[3-36], identified herein as SEQ ID NO: 3. Polypeptides with numbers in brackets refer to truncated polypeptides having the sequence of the full length peptide over the amino acid positions in the brackets. Thus, PYY[3-36] has a sequence identical to PYY over amino acids 3 to 36. A PYY agonist may bind to a PYY receptor with higher or lower affinity, demonstrate a longer or shorter half-life in vivo or in vitro, or be more or less effective than native PYY.

Problems solved by technology

Obesity and its associated disorders are common and very serious public health problems in the United States and throughout the world.
It reduces life-span and carries a serious risk of co-morbidities above, as well disorders such as infections, varicose veins, acanthosis nigricans, eczema, exercise intolerance, insulin resistance, hypertension hypercholesterolemia, cholelithiasis, orthopedic injury, and thromboembolic disease (Rissanen, Heliovaara et al.
The pathogenesis of obesity is believed to be multifactoral but the basic problem is that in obese subjects nutrient availability and energy expenditure do not come into balance until there is excess adipose tissue.
Obesity is currently a poorly treatable, chronic, essentially intractable metabolic disorder.

Method used

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  • Peptide YY and Peptide YY Agonists for Treatment of Metabolic Disorders
  • Peptide YY and Peptide YY Agonists for Treatment of Metabolic Disorders
  • Peptide YY and Peptide YY Agonists for Treatment of Metabolic Disorders

Examples

Experimental program
Comparison scheme
Effect test

example 1

Activity of Y Receptor Ligands on Food Intake in Overnight-Fasted NIH / SW Mice

[0055]Female NIH / Swiss mice (8-12 weeks old) were group housed with a 12:12 hour light:dark cycle with lights on at 0600. Water and a standard pelleted mouse chow diet were available ad libitum, except as noted. Animals were fasted and housed individually starting at approximately 1500 hrs, 1 day prior to experiment. The morning of the experiment (approx. 0630 hrs), all animals were weighed and divided into experimental groups so as to give the most similar weight distribution between groups. In a typical study, n=10 for the control group and at least 5 for each treatment group.

[0056]At time=0 min, all animals were given an intraperitoneal injection of vehicle or compound in a volume of 5 ml / kg and immediately given a pre-weighed amount (10-15 g) of the standard chow. Increasing dosages of PYY[3-36], or PYY (0.1 μg / kg to 500 μg / kg and NPY (100 and 500 μg / kg), and single high doses of NPY[3-36] (100 μg / kg), ...

example 2

Activity of Y Peptide Ligands on Gastric Emptying in HSD Rats

[0061]Male HSD rats, 180-215 g, were housed with a 12:12 hour light:dark cycle and fasted for 20 hrs (overnight). At time=0 min, test peptide (PYY[3-36], PYY, Ac-PYY[22-36], NPY, NPY[3-36], or PP) or saline vehicle was injected (intraperitoneal) into conscious rats (n=6 / group). At t=1 min, a solution of 1 mL sterile water containing 5 μCi of 3H-3-O-methyl-glucose was gavaged by oropharyngeal tube to conscious rats. Blood samples (10 μl) were collected 40 min after gavage and assayed for counts per minute (CPM) in plasma. To eliminate pain during tail vein sampling, 2% Lidocaine (0.1 ml) was injected 3-4 cm from the end of the tail (Gedulin, Jodka et al. Gastroenterology 108: A604, 1995).

Data Analysis:

[0062]Effects of the test compound were expressed as percent change relative to control, which was calculated as −100*(1-(mean value test rats / mean value controls)).

[0063]Relative activity was defined as significant if p<0.05 ...

example 3

Acute Peripheral Administration of PYY[3-36] Inhibits Gastric Acid Secretion in Rats

[0065]Male Harlan Sprague Dawley rats were housed in a 12:12 hour light:dark cycle. All experiments were performed during the light cycle. Animals were fasted for approximately 20 hours before experimentation but were given free access to water until the start of the experiment.

[0066]Rats (age 11-16 weeks, body mass 291-365 g) were surgically fitted with gastric fistulae (Kato, Martinez et al. Peptides 16: 1257-1262, 1995). Overnight fasted rats were weighed and their gastric fistulae were uncapped and attached to flexible Tygon tubing (⅜× 1 / 16) into which was fitted a piece of PE205 tubing that would extend up into the stomach. Saline was injected through the narrower PE205 tubing and the effluent collected from the Tygon tubing. To ensure proper flow through the fistulae and an empty stomach, the stomach was flushed several times with ˜5 mL of room temperature saline solution until flow was easy an...

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Abstract

Methods and compositions are disclosed to treat metabolic disorders such as obesity, diabetes, and increased cardiovascular risk comprising administering a therapeutically effective amount of a PYY or a PYY agonist.

Description

CROSS-REFERENCE TO RELATED APPLICATION[0001]This application is a continuation of and claims priority to pending U.S. patent application Ser. No. 10 / 016,969, entitled “Peptide YY and Peptide YY Agonists for Treatment of Metabolic Disorders,” filed Dec. 14, 2001, and claims priority to U.S. Provisional Application Ser. No. 60 / 256,216 entitled “Peptide YY and Peptide YY Agonists for Treatment of Obesity, Diabetes, and other Metabolic Disorders,” filed Dec. 15, 2000, each of which are hereby incorporated by reference in their entirety.FIELD OF THE INVENTION[0002]The present invention relates to methods and compositions for treating metabolic conditions or disorders, particularly those which can be alleviated by reducing caloric availability, for example diabetes, obesity, eating disorders, insulin-resistance syndrome (Syndrome X), glucose intolerance, dyslipidemia, and cardiovascular disorders.BACKGROUND[0003]A number of related hormones make up the pancreatic polypeptide (PP) family. ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K38/22A61P3/04A61P9/12A61P9/00A61P3/10A61P3/06A61K35/38A61K38/17A61K45/00A61P3/08C07K14/575
CPCA61K35/38A61K38/2271A61K38/22A61P3/04A61P3/12A61P3/06A61P3/08A61P9/00A61P9/12A61P3/10
Inventor PITTNER, RICHARD A.YOUNG, ANDREW A.PATERNITI, JR., JAMES R.
Owner ASTRAZENECA PHARMA LP
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