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Endocannabinoid and nitric oxide systems of the hypothalamic paraventricular nucleus mediate effects of NPY on energy expenditure
- Source :
- Molecular metabolism, Molecular metabolism, Elsevier, 2018, 18, pp.120-133. ⟨10.1016/j.molmet.2018.08.007⟩, Molecular Metabolism, Molecular metabolism, 2018, 18, pp.120-133. ⟨10.1016/j.molmet.2018.08.007⟩, Molecular Metabolism, Vol 18, Iss, Pp 120-133 (2018)
- Publication Year :
- 2018
- Publisher :
- HAL CCSD, 2018.
-
Abstract
- Objective Neuropeptide Y (NPY) is one of the most potent orexigenic peptides. The hypothalamic paraventricular nucleus (PVN) is a major locus where NPY exerts its effects on energy homeostasis. We investigated how NPY exerts its effect within the PVN. Methods Patch clamp electrophysiology and Ca2+ imaging were used to understand the involvement of Ca2+ signaling and retrograde transmitter systems in the mediation of NPY induced effects in the PVN. Immuno-electron microscopy were performed to elucidate the subcellular localization of the elements of nitric oxide (NO) system in the parvocellular PVN. In vivo metabolic profiling was performed to understand the role of the endocannabinoid and NO systems of the PVN in the mediation of NPY induced changes of energy homeostasis. Results We demonstrated that NPY inhibits synaptic inputs of parvocellular neurons in the PVN by activating endocannabinoid and NO retrograde transmitter systems via mobilization of Ca2+ from the endoplasmic reticulum, suggesting that NPY gates the synaptic inputs of parvocellular neurons in the PVN to prevent the influence of non-feeding-related inputs. While intraPVN administered NPY regulates food intake and locomotor activity via NO signaling, the endocannabinoid system of the PVN selectively mediates NPY-induced decrease in energy expenditure. Conclusion Thus, within the PVN, NPY stimulates the release of endocannabinoids and NO via Ca2+-influx from the endoplasmic reticulum. Both transmitter systems appear to have unique roles in the mediation of the NPY-induced regulation of energy homeostasis, suggesting that NPY regulates food intake, energy expenditure, and locomotor activity through different neuronal networks of this nucleus.<br />Graphical abstract Image 1<br />Highlights • NPY increases the intracellular Ca2+ level of PVN neurons by mobilizing the Ca2+ from ER. • NPY inhibits the input of these neurons by endocannabinoids and NO. • IntraPVN administered NPY regulates food intake and locomotor activity via NO signaling. • IntraPVN administered NPY regulates energy expenditure via the endocannabinoid system. • NPY regulates the energy expenditure and food intake via different neuronal networks of the PVN.
- Subjects :
- 0301 basic medicine
Male
STIMULATION
[SDV]Life Sciences [q-bio]
Energy homeostasis
ACTIVATION
chemistry.chemical_compound
Mice
Neuropeptide Y
GENE-EXPRESSION
digestive, oral, and skin physiology
Synaptic Potentials
Neuropeptide Y receptor
Endocannabinoid system
humanities
3. Good health
Cell biology
[SDV] Life Sciences [q-bio]
RECEPTORS
medicine.anatomical_structure
NEUROPEPTIDE-Y
Original Article
hormones, hormone substitutes, and hormone antagonists
medicine.drug
lcsh:Internal medicine
SYNTHESIZING NEURONS
HORMONE GENE
NPY
Nitric oxide
RATS
03 medical and health sciences
Parvocellular cell
Orexigenic
mental disorders
medicine
Animals
Calcium Signaling
lcsh:RC31-1245
Molecular Biology
Endocannabinoid
INNERVATION
SUPPRESSION
Endoplasmic reticulum
Cell Biology
030104 developmental biology
chemistry
nervous system
Hypothalamic paraventricular nucleus
Energy Metabolism
Nucleus
Endocannabinoids
Paraventricular Hypothalamic Nucleus
Subjects
Details
- Language :
- English
- ISSN :
- 22128778
- Database :
- OpenAIRE
- Journal :
- Molecular metabolism, Molecular metabolism, Elsevier, 2018, 18, pp.120-133. ⟨10.1016/j.molmet.2018.08.007⟩, Molecular Metabolism, Molecular metabolism, 2018, 18, pp.120-133. ⟨10.1016/j.molmet.2018.08.007⟩, Molecular Metabolism, Vol 18, Iss, Pp 120-133 (2018)
- Accession number :
- edsair.doi.dedup.....82e72a3f6498019486203652820415b3
- Full Text :
- https://doi.org/10.1016/j.molmet.2018.08.007⟩