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Review Article
Drug Therapy
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Volume 334:246-254 January 25, 1996 Number 4
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Octreotide
Steven W.J. Lamberts, M.D., Ph.D., Aart-Jan van der Lely, M.D., Ph.D., Wouter W. de Herder, M.D., Ph.D., and Leo J. Hofland, Ph.D.

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A peptide inhibiting the release of growth hormone was originally detected accidentally during studies of the distribution of growth hormone–releasing factor in the hypothalamus of rats.1 This peptide, called somatostatin, proved to be a cyclic peptide consisting of 14 amino acids.2 Subsequent work has considerably expanded this initially simple concept of somatostatin as a peptide whose main function is the regulation of growth hormone secretion.3 Today, somatostatin is best regarded as a phylogenetically ancient, multigene family of peptides with two important bioactive products: somatostatin-14 and somatostatin-28, the latter a congener of somatostatin-14 extended at the N-terminal.3,4

Like other peptide hormones, . . . [Full Text of this Article]

Somatostatin Receptors

Somatostatin Analogues

Treatment of Hormone-Secreting Tumors

Acromegaly

Thyrotropin-Secreting Pituitary Adenomas

Nonsecretory Pituitary Adenomas

Corticotropin-Secreting Pituitary Adenomas

Pancreatic Islet-Cell Tumors

Carcinoid Tumors

Gastrointestinal Indications

Potential Role in Oncologic Treatment

Adverse Effects of Octreotide

New Forms of Somatostatin Analogues

Conclusions


Source Information

From the Department of Medicine, Erasmus University, Rotterdam, the Netherlands.

Address reprint requests to Dr. Lamberts at University Hospital Dijkzigt, 40 Dr. Molewaterplein, 3015 GD Rotterdam, the Netherlands.

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