Issue 4, 2011

Anticonvulsant neuropeptides as drug leads for neurological diseases

Abstract

Covering: 1995 to 2010

Anticonvulsant neuropeptides are best known for their ability to suppress seizures and modulate pain pathways. Galanin, neuropeptide Y, somatostatin, neurotensin, dynorphin, among others, have been validated as potential first-in-class anti-epileptic or/and analgesic compounds in animal models of epilepsy and pain, but their therapeutic potential extends to other neurological indications, including neurodegenerative and psychatric disorders. Disease-modifying properties of neuropeptides make them even more attractive templates for developing new-generation neurotherapeutics. Arguably, efforts to transform this class of neuropeptides into drugs have been limited compared to those for other bioactive peptides. Key challenges in developing neuropeptide-based anticonvulsants are: to engineer optimal receptor-subtype selectivity, to improve metabolic stability and to enhance their bioavailability, including penetration across the blood–brain barrier (BBB). Here, we summarize advances toward developing systemically active and CNS-penetrant neuropeptide analogs. Two main objectives of this review are: (1) to provide an overview of structural and pharmacological properties for selected anticonvulsant neuropeptides and their analogs and (2) to encourage broader efforts to convert these endogenous natural products into drug leads for pain, epilepsy and other neurological diseases.

Graphical abstract: Anticonvulsant neuropeptides as drug leads for neurological diseases

Article information

Article type
Review Article
Submitted
29 Sep 2010
First published
21 Feb 2011

Nat. Prod. Rep., 2011,28, 741-762

Anticonvulsant neuropeptides as drug leads for neurological diseases

C. R. Robertson, S. P. Flynn, H. S. White and G. Bulaj, Nat. Prod. Rep., 2011, 28, 741 DOI: 10.1039/C0NP00048E

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