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Application of Genetically Encoded Fluorescent Nitric Oxide (NO•) Probes, the geNOps, for Real-time Imaging of NO• Signals in Single Cells
Published on: March 16, 2017
Nitric oxide modulates ATP-evoked currents in mouse Leydig cells
J L de Deus1, A L A Dagostin1, W A Varanda1
1Departamento de Fisiologia, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
Nitric oxide (NO) positively modulates ATP-evoked calcium currents in mouse Leydig cells via the NO/cGMP pathway, revealing a novel interaction between purinergic and nitrergic systems in testosterone synthesis regulation.
Area of Science:
- Endocrinology
- Cell Physiology
- Neuroendocrinology
Background:
- Testosterone synthesis in Leydig cells is calcium-dependent.
- Calcium regulation involves purinergic receptors and nitric oxide (NO).
- NO is known to inhibit testosterone production.
Purpose of the Study:
- Investigate the interaction between purinergic and nitrergic systems in mouse Leydig cells.
- Determine NO's role in regulating ATP-evoked calcium currents.
Main Methods:
- Whole-cell patch clamp technique on isolated adult mouse Leydig cells.
- Application of ATP, L-NAME, L-arginine, ODQ, and 8-Br-cGMP.
- Measurement of ATP-evoked currents.
Main Results:
- Basal NO levels in Leydig cells do not affect ATP-evoked currents.
- Supplemental L-arginine (300 μM) enhances ATP-evoked currents.
- This enhancement involves the NO/cGMP signaling pathway.
Conclusions:
- A functional interaction exists between the nitrergic and purinergic systems in Leydig cells.
- Nitric oxide positively modulates calcium (Ca2+) entry through purinergic receptors.
- This NO-mediated regulation impacts Leydig cell function and potentially testosterone synthesis.
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