Novel neurotransmitters for sleep and energy homeostasis
1Department of Molecular Biology, Scripps Research Institute, La Jolla, California 92037, USA.
Insights
Researchers identified novel brain peptides, cortistatin and hypocretin, regulating sleep and feeding behaviors. These peptides, derived from specific mRNAs, demonstrate distinct physiological effects and are linked to homeostatic regulation.
Area of Science:
- Neuroscience
- Molecular Biology
- Peptide Research
Background:
- Identifying brain-specific mRNAs is crucial for understanding neuronal function.
- Peptides play vital roles in regulating complex behaviors like sleep and feeding.
Purpose of the Study:
- To identify and characterize novel mRNAs with restricted brain expression.
- To investigate the physiological roles of the peptides encoded by these mRNAs, specifically cortistatin and hypocretin.
Main Methods:
- Development of methodologies for identifying restricted brain mRNAs.
- Analysis of peptide precursor sequences and their homology to known peptides.
- Immunohistochemical detection of peptides in neuronal pathways.
- Electrophysiological application of peptides to cultured neurons.
- Behavioral studies on the effects of peptides on locomotor activity, sleep, and feeding.
Main Results:
- A novel mRNA encoding preprocortistatin was identified, restricted to GABAergic interneurons; the resulting peptide, cortistatin, regulates sleep and cortical excitability.
- A second mRNA encoding preprohypocretin was identified, restricted to hypothalamic neurons; the resulting peptides (orexins) stimulate feeding behavior.
- Both cortistatin and hypocretin peptides are regulated by physiological states (sleep deprivation and food deprivation, respectively).
- A single amino acid difference distinguishes cortistatin from somatostatin, leading to distinct physiological effects.
Conclusions:
- Peptide transmitters derived from transcription-based mRNA accumulation regulate essential voluntary behaviors.
- Cortistatin and hypocretin represent key regulators of sleep and feeding, respectively.
- These findings reveal a common regulatory mechanism for homeostatic behaviors involving peptide accumulation and neural circuit modulation.
Abstract:
We have developed methodologies for identifying mRNAs with highly restricted expression within the brain. One postnatal-onset mRNA, restricted to sparse GABAergic interneurons of the cerebral cortex and hippocampus, encodes preprocortistatin, the precursor of a 14-residue peptide that shares 11 amino acids with somatostatin. Cortistatin binds to all five cloned somatostatin receptors when they are expressed in transfected cells and depresses neuronal activity, but, unlike somatostatin, it reduces locomotor activity and induces slow-wave sleep. Cortistatin, whose mRNA accumulates during sleep deprivation, apparently acts by antagonizing the effects of acetylcholine on cortical excitability, thereby causing synchronization brain slow waves. A single amino acid difference with somatostatin accounts for the dramatic differences in the effects of the two peptides on physiology and behavior. A second postnatal-onset mRNA, restricted to 1100 large neuronal cell bodies of the dorsal-lateral hypothalamus, encodes preprohypocretin, the precursor of two peptides that share homology with each other and with members of the secretin peptide family. The peptides are detected immunohistochemically in secretory vesicles at synapses of fibers that project to posterior hypothalamus and diverse targets in other brain regions. The peptides are excitatory when applied to cultured hypothalamic neurons. Recent studies by Sakurai and colleagues (1998) have identified the hypocretin peptides (called the orexins by those workers) as ligands for two orphan receptors at which they stimulate food-intake behavior. Sakurai and collaborators showed that the mRNA for these peptides accumulates during food deprivation. The hypocretin projections suggest additional homeostatic roles for the peptides. These studies suggest the common mechanism of regulation for necessary, but voluntary, behaviors (sleep and feeding) by transcription-based accumulation of peptide transmitters that create a pressure for the voluntary activities.
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