Methods of using a neurotrophin and its analogues for the...

Drug – bio-affecting and body treating compositions – Antigen – epitope – or other immunospecific immunoeffector – Hormone or other secreted growth regulatory factor,...

Reexamination Certificate

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C514S021800

Reexamination Certificate

active

06656474

ABSTRACT:

1. FIELD OF INVENTION
This invention relates to methods of treating gastrointestinal hypomotility disorders. In particular, it relates to methods of using a neurotrophin and its analogues enhance gastrointestinal motility.
2. BACKGROUND OF INVENTION
Constipation, which is the passage of less than 3 bowel movements per week with excessive straining at least 25% of the time, is the most common gastrointestinal complaint in the United States, resulting in about 2 million annual visits to the clinic. (See, National Digestive Diseases Information Clearinghouse) In addition, Americans spend $725 million on laxatives each year without seeking medical help. According to the 1991 National Health Interview Survey, about 4.5 million people in the United States say they are constipated most or all of the time.
Constipation is one of the most common forms of gastrointestinal hypomotility disorders. Constipation also occurs with a number of other conditions including, but not limited to abdominal pain, abdominal cramps, irritable bowel syndrome, non-tropical sprue, megacolon associated with hypothyroidism, pseudo-obstruction of the gastrointestinal tract, colitis, hypomotility of the colon associated with diabetes mellitus, adult onset Hirschsprung's disease, neurological disorders, myopathic disorders, spinal cord injury, Parkinson's disease, jejunal-ileal bypass with secondary megacolon, cancer chemotherapy, critical illness including severe burns and other major stresses, with syndromes of depression, the post-operative state, and other pathological conditions.
Gastrointestinal hypomotility disorders also include disorders of the esophagus and gastric-motility including gastric emptying disorders such as diabetic gastroparesis and those that are associated with scleroderma.
Hypomotility may be associated with recurring bouts of hypermotility, the so-called intermittent hypomotility-hypermotility (or irritable bowel) syndrome. Clinical manifestations of this affliction include alternate bouts of constipation and diarrhea, abdominal distention, pains and cramps often relieved by passage of stool. Constipation may also occur in inflammation of gastrointestinal disorders such as ileitis, regional ententes ulcerative and other forms of colitis.
The digestive system functions to process nutrients and other food substances for efficient absorption by the cells of the body. When food is ingested, large particles are broken into smaller particles, enzymes are secreted to decompose food molecules, the products of the digestive action are absorbed, and unused residue is eliminated. In the alimentary canal of the digestive system, food and materials which are by-products of the digestive process are moved along by peristalsis—movement resulting from waves of alternate circular contraction and relaxation of the tubular structure of the canal by which the contents are propelled onward.
In the context of the present invention, motility consists of normal spontaneous coordinated distensions and contractions of the stomach, intestines, colon and rectum to move food through the gastrointestinal tract during the digestive process. Hypomotility disorders are those in which contractions are not occurring naturally or are abnormally slow, resulting in delayed passage of gut contents from stomach to anus. The disorder of unknown cause (idiopathic) in some 50% of the cases (Sleisenger et al., 1989
, Gastrointestinal Disease
, 4th ed., HBJ, Inc., Philadelphia, pp. 675-713).
Current forms of therapy for such hypomotility syndromes include treatment of the underlying disorder, dietary support, and use of prokinetic agents such as metoclopramide and cisapride (propulsid). In some instances, surgery may be required.
Although metoclopramide is most often prescribed among hypomotility patients, at least one study has indicated that this drug is effective in only 60% of patients with diabetic gastroparesis, and in only 25% of patients with prior gastric surgery (See e.g., Drug Evaluations, 6th ed., AMA, Chicago, 1986, p. 953). In addition, there is evidence that the effectiveness of metoclopramide dissipates with long term use. This appears to be the case at least where diabetes is the underlying disease (Schade et al., 1985
, Dig. Dis. Sci
., 30:10-15 ). The long term value of the drug has not been established for treating gastric stasis which is either idiopathic or attributed to gastric ulcer.
Another reported disadvantage of metoclopramide therapy is that 20% to 30% of user patients experience side effects including drowsiness, restlessness, anxiety, tremor and muscle rigidity. (see, Sleisenger et al., Id.). In younger patients, metoclopramide frequently causes acute dystonic reactions such as torticollis, trismus, facial spasma, and opisthotonos. Id. In elderly patients, metoclopramide causes Parkinsonian reaction and irreversible tardive dyskinesia. Id. Other side effects of metoclopramide include hyperprolactinemia and subsequent impotence, gynecomastia, amenorrhea, or galactorrhea. Id.
Cisapride is a benzamide and its effects on the motility of the stomach and small bowel closely resemble those of metoclopramide; however, unlike metoclopramide, it also increases colonic motility and can cause diarrhea. (Brunton, 1990
, Agents Affecting Gastrointestinal Water Flux and Motility, Digestants, and Bile Acids
, in
Pharmacological Basis of Therapeutics
, Gilman et al., eds., p. 929, Pergamon Press, New York.) The mechanism of cisapride's gastrointestinal actions is poorly understood. Like metoclopramide, cisapride's actions are blocked by atropine and may involve the release of myenteric acetylcholine. Id. Cisapride appears to be devoid of dopaminergic blocking activity. Because it lacks central antidopaminergic effects, it does not influence the concentration of prolactin in plasma or cause extrapyramidal symptoms.
However, particularly in combination with other drugs (e.g., antifungals such as ketoconazole, itraconazole, and fluconazole; antibacterials such as erythromycin, clarithromycin, and troleandomycin; and HIV protease inhibitors ritonavir and indinavir), cisapride can cause serious ventricular arrhythmais and sudden death. (1990
, New Warnings Added to Cisapride Labeling
, JAMA 280:410). The common side effects of cisapride include abdominal cramping, diarrhea, and headache, which lead to drug discontinuation in 2% to 3% of patients.
Thus, there remains a need for improved compositions and methods for treating gastrointestinal hypomobility disorders such as constipation.
3. SUMMARY OF INVENTION
The present invention relates to the treatment of gastrointestinal hypomotility, particulary human acute and chronic constipation. More specifically, the invention relates to the use of a neurotrophin for the treatment of gastrointestinal hypomotility.
The invention is based, in part, on the inventor's discovery that neurotrophin-3 (NT-3) enhances gastrointestinal motility as measured by different parameters. The administration of NT-3 in humans improves stool frequency, colonic motility, gastric emptying and small bowel transit time, with minimal adverse side effects. Both healthy subjects and patients with constipation responded to NT-3 treatment.
One aspect of the present invention provides methods and compositions for the treatment of gastrointestinal hypomotility, typically, chronic constipation, obstipation, idiopathic abdominal distention, irritable bowel syndrome, megacolon associated with hypothyroidism, pseudo-obstruction of the gastrointestinal tract, hypomotility of the stomach and colon associated with diabetes mellitus, neurological disorders, myopathic disorders, spinal cord injury, Parkinson's disease, geriatric hypomotility disorders, jejunal-ileal bypass with secondary megacolon, hypomotility associated with cancer chemotherapy, hypomotility associated with severe burns and other major stresses, hypomotility associated with syndromes of depression, post-operative intestinal distension, and other pathological conditions, in a subject in need of such treatment. The subje

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