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Antisense strategies in dopamine receptor pharmacology
Review   Peer reviewed

Antisense strategies in dopamine receptor pharmacology

Benjamin Weiss, Sui-Po Zhang and Long-Wu Zhou
Life Sciences, v 60(7), pp 433-455
1997
PMID: 9042372

Abstract

6-hydroxydopamine antisense antisense localization body temperature D 1 dopamine receptor D 2 dopamine receptor D 3 dopamine receptor dopamine receptor dopamine receptor mRNA dopamine receptor pools dopamine receptor subtypes dopaminergic behavior fluphenazine-N-mustard intraventricular molecular biology oligodeoxynucleotide quinpirole receptor synthesis SKF 38393
Recent advances in molecular biology have rovided pharmacologists the opportunity of developing an entirely new type of agent for studying and treating a variety of biological disorders. These agents, termed antisense oligodeoxynucleotides, have as their target the messenger RNAs encoding specific proteins. They act by binding to selected portions of these mRNAs through complimentary interactions and thereby prevent the synthesis of these proteins. These novel pharmacological tools have the promise of being easier to design and being more selective and predictable in their actions. In addition, insofar as agents targeted to receptors for neurotransmitters are concerned, unlike the classical pharmacological agents, these new compounds may not lead to the upregulation of the very receptors the drugs are designed to inhibit.

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Web of Science research areas
Medicine, Research & Experimental
Pharmacology & Pharmacy
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