Use of somatostatin receptor agonists in the treatment of human disorders of sleep hypoxia and oxygen deprivation

• US 20030083241A1
• Filed: 10/25/2002
• Published: 05/01/2003
• Est. Priority Date: 11/01/2001
• Status: Abandoned Application

• Current Assignee: Charles W. Young
• Original Assignee: Charles W. Young
• Inventors: Young, Charles W.
• Application Number:
  US10/280,517
• Publication Number:
  US 20030083241A1
• Time in Patent Office: Days
• US Class Current: 514/9
• CPC Class Codes: A61K 38/31 Somatostatins

Abstract

The invention relates to a method of treating diverse human disorders that may arise, in part, out of sleep hypoxia and oxygen deprivation occurring in the context of sleep apnea/hypopnea disturbances. The disorders that may be treated by the invention comprise gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma, asthma, cardiomyopathy, cardioarrhythmia, congestive heart failure, sudden infant death syndrome, and diverse neurologic conditions. The mode of treatment uses somatostatin receptor ligands (SstRLs), particularly somatostatin-receptor agonists. The invention concerns the method of treatment utilizing, and compositions comprising SstRLs and somatostatin receptor agonists, including agonists of the somatostatin receptor types 2 and 5, particularly, the type 2A receptor (SsR-2A), including octreotide and lanreotide.

Claims

1. A method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering an effective amount of a composition comprising a somatostatin receptor agonist to a human patient in need thereof.

2. The method according to claim 1, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

3. The method according to claim 1, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

4. The method according to claim 1, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

5. The method according to claim 1, wherein the somatostatin receptor agonist is octreotide acetate.

6. The method according to claim 1, wherein the somatostatin receptor agonist is lanreotide.

7. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit pepsinogen secretion and its activation to pepsin to a human patient in need thereof.

8. The method according to claim 7, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

9. The method according to claim 7, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

10. The method according to claim 7, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

11. The method according to claim 7, wherein the somatostatin receptor agonist is octreotide acetate.

12. The method according to claim 7, wherein the somatostatin receptor agonist is lanreotide.

13. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to increase lower esophageal sphincter pressure to a human patient in need thereof.

14. The method according to claim 13, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

15. The method according to claim 13, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

16. The method according to claim 13, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

17. The method according to claim 13, wherein the somatostatin receptor agonist is octreotide acetate.

18. The method according to claim 13, wherein the somatostatin receptor agonist is lanreotide.

19. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to increase intraesophageal body pressure and motility to a human patient in need thereof.

20. The method according to claim 19, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

21. The method according to claim 19, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

22. The method according to claim 19, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

23. The method according to claim 19, wherein the somatostatin receptor agonist is octreotide acetate.

24. The method according to claim 19, wherein the somatostatin receptor agonist is lanreotide.

25. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to reduce esophageal exposure to acid to a human patient in need thereof.

26. The method according to claim 25, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

27. The method according to claim 25, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

28. The method according to claim 25, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

29. The method according to claim 25, wherein the somatostatin receptor agonist is octreotide acetate.

30. The method according to claim 25, wherein the somatostatin receptor agonist is lanreotide.

31. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to decrease the rate of entry of bile, bile salts and proteolytic enzymes into the duodenum, thereby decreasing the quantity of bile acids and proteolytic enzymes present within the duodenal contents to a human patient in need thereof.

32. The method according to claim 31, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

33. The method according to claim 31, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

34. The method according to claim 31, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

35. The method according to claim 31 wherein the somatostatin receptor agonist is octreotide acetate.

36. The method according to claim 31, wherein the somatostatin receptor agonist is lanreotide.

37. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to decrease the rate of secretion of cholecystokinin to a human patient in need thereof.

38. The method according to claim 37, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

39. The method according to claim 37, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

40. The method according to claim 37, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

41. The method according to claim 37, wherein the somatostatin receptor agonist is octreotide acetate.

42. The method according to claim 37, wherein the somatostatin receptor agonist is lanreotide.

43. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to decrease an excessive rate of secretion within the brain and/or the peripheral nervous system of pituitary adenylate cyclase activating peptide (PACAP) and vasoactive intestinal peptide (VIP), and to inhibit the excessive activation of endothelial nitric oxide synthase or of inducible nitric oxide to a human patient in need thereof.

44. The method according to claim 43, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

45. The method according to claim 43, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

46. The method according to claim 43, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

47. The method according to claim 43, wherein the somatostatin receptor agonist is octreotide acetate.

48. The method according to claim 43, wherein the somatostatin receptor agonist is lanreotide.

49. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to produce parallel constrictive effects on the LES and the sphincter of Oddi to a human patient in need thereof.

50. The method according to claim 49, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

51. The method according to claim 49, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

52. The method according to claim 49, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

53. The method according to claim 49, wherein the somatostatin receptor agonist is octreotide acetate.

54. The method according to claim 49, wherein the somatostatin receptor agonist is lanreotide.

55. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the synthesis and release of TNF-alpha, IL-1 beta, and INF-gamma by monocytes and T-cell lymphocytes to a human patient in need thereof.

56. The method according to claim 55, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

57. The method according to claim 55, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

58. The method according to claim 55, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

59. The method according to claim 55, wherein the somatostatin receptor agonist is octreotide acetate.

60. The method according to claim 55, wherein the somatostatin receptor agonist is lanreotide.

61. The method of preventing or treating gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the activation of NF-kappaB and c-fos/AP-1 nuclear transcription factors to a human patient in need thereof.

62. The method according to claim 61, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

63. The method according to claim 61, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

64. The method according to claim 61, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

65. The method according to claim 61, wherein the somatostatin receptor agonist is octreotide acetate.

66. The method according to claim 61, wherein the somatostatin receptor agonist is lanreotide.

67. The method of preventing or treating sleep apnea/hypopnea-associated episodes of hypoxemia and tissue hypoxia, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the synthesis and/or secretion within the brain and/or the peripheral nervous system of excessive quantities of somnogenic peptides, and to inhibit or blunt the central and peripheral actions thereof, to a human patient in need thereof.

68. The method according to claim 67, wherein the somnogenic peptides are selected from the group consisting of growth hormone releasing hormone (GHRH), pituitary adenylate cyclase activating peptide (PACAP), vasoactive intestinal peptide (VIP), TNF-alpha, cortistatin, IL-6, and IL-1 beta.

69. The method according to claim 67, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

70. The method according to claim 67, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

71. The method according to claim 67, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

72. The method according to claim 67, wherein the somatostatin receptor agonist is octreotide acetate.

73. The method according to claim 67, wherein the somatostatin receptor agonist is lanreotide.

74. The method of preventing or treating sleep apnea/hypopnea-associated gastroesophageal reflux disease (GERD), asthma-associated gastroesophageal reflux (GER), GER-associated asthma and asthma, or related disorders, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the synthesis and/or secretion within the brain and/or the peripheral nervous system of excessive quantities of somnogenic peptides, and to inhibit or blunt the peripheral actions thereof, to a patient in need thereof.

75. The method according to claim 74, wherein the somnogenic peptides from the group consisting of pituitary adenylate cyclase activating peptide (PACAP), vasoactive intestinal peptide (VIP), TNF-alpha, and IL-1 beta.

76. The method according to claim 74, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

77. The method according to claim 74, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

78. The method according to claim 74, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

79. The method according to claim 74, wherein the somatostatin receptor agonist is octreotide acetate.

80. The method according to claim 74, wherein the somatostatin receptor agonist is lanreotide.

81. The method of preventing or treating sleep apnea/hypopnea-associated and or sleep apnea/hypopnea-aggravated cardiomyopathy, cardioarrhythmia, and congestive heart failure, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the secretion within the brain and/or the peripheral nervous system of excessive quantities of somnogenic peptides, and to inhibit or blunt the central and peripheral actions thereof, to a human patient in need thereof.

82. The methods according to claim 81, wherein the somnogenic peptides are selected from the group consisting of growth hormone-releasing hormone (GHRH), pituitary adenylate cyclase activating peptide (PACAP), vasoactive intestinal peptide (VIP) TNF-alpha, and IL-1 beta.

83. The method according to claim 81, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

84. The method according to claim 81, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

85. The method according to claim 81, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

86. The method according to claim 81, wherein the somatostatin receptor agonist is octreotide acetate.

87. The method according to claim 81, wherein the somatostatin receptor agonist is lanreotide.

88. The method of preventing or treating sleep apnea/hypopnea-associated and/or sleep apnea/hypopnea-aggravated apparent life-threatening events (ALTE), referred to as a “

near miss”

for sudden infant death syndrome (SIDS), which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the secretion within the brain and/or the peripheral nervous system of excessive quantities of somnogenic peptides, and to inhibit or blunt the central and peripheral actions thereof, to a human patient in need thereof.

89. The method according to claim 88, wherein the somnogenic peptides are selected from the group consisting of growth hormone-releasing hormone (GHRH), pituitary adenylate cyclase activating peptide (PACAP) vasoactive intestinal peptide (VIP), TNF-alpha, and IL-1 beta.

90. The method according to claim 88, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

91. The method according to claim 88, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

92. The method according to claim 88, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

93. The method according to claim 88, wherein the somatostatin receptor agonist is octreotide acetate.

94. The method according to claim 88, wherein the somatostatin receptor agonist is lanreotide.

95. The method of preventing or treating sleep apnea/hypopnea-associated and/or sleep apnea/hypopnea-aggravated neurologic disorders selected from the group consisting of median nerve compression neuropathy (carpal tunnel syndrome), motor and cognitive dysfunction post-cerebrovascular occlusion or hemorrhage, post-ischemia-reperfusion injury, cerebral arteriosclerosis, Alzheimer'"'"'s disease, amyotrophyic lateral sclerosis (ALS), myasthenia gravis, central nervous system trauma, and alcoholism/post-alcoholism syndrome, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the secretion within the brain and/or the peripheral nervous system of excessive quantities of somnogenic peptides, and to inhibit or blunt the central and peripheral actions thereof, to a human patient in need thereof.

96. The method according to claim 95, wherein the somnogenic peptides are selected from the group consisting of growth hormone-releasing hormone (GHRH), pituitary adenylate cyclase activating peptide (PACAP) vasoactive intestinal peptide (VIP), TNF-alpha, and IL-1 beta.

97. The method according to claim 96, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

98. The method according to claim 96, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

99. The method according to claim 96, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

100. The method according to claim 96, wherein the somatostatin receptor agonist is octreotide acetate.

101. The method according to claim 96, wherein the somatostatin receptor agonist is lanreotide.

102. The method of preventing or treating disorders of excessive or undesired calpain activation arising from or aggravated by tissue hypoxia, selected from the group consisting of sleep apnea/hypopnea-induced tissue hypoxia, ischemia/reperfusion injury, direct physical injury, which method comprises administering a composition comprising an effective amount of a somatostatin receptor agonist sufficient to inhibit the activation of calpain in tissues with appropriate somatostatin receptors, to a human patient in need thereof.

103. The method according to claim 102, wherein the tissues are selected from the group consisting of tissues of the peripheral and central nervous systems, heart liver, kidney and gastrointestinal tract.

104. The method according to claim 102, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin receptor types 2 and 5.

105. The method according to claim 102, wherein the somatostatin receptor agonist is selected from the group consisting of agonists of somatostatin type 2A receptor.

106. The method according to claim 102, wherein the somatostatin receptor agonist is selected from the group consisting of non-peptide somatostatin agonists.

107. The method according to claim 102, wherein the somatostatin receptor agonist is octreotide acetate.

108. The method according to claim 102, wherein the somatostatin receptor agonist is lanreotide.