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Updated: May 10, 2025

Dissection of Pelvic Autonomic Ganglia and Associated Nerves in Male and Female Rats
Published on: March 7, 2020
SST neurons in the periaqueductal gray regulate urination and bladder function
Junan Yan1,2,3, Ziyan Gao4, Xianping Li5,6
1Center for Neurointelligence, School of Medicine, Chongqing University, Chongqing, China. junan_yan@aliyun.com.
Scientists identified somatostatin (SST)-expressing neurons in the periaqueductal gray (PAG) that control urination. Activating these neurons triggers urination, while inhibiting them stops it, revealing a key pathway for bladder control.
Area of Science:
- Neuroscience
- Urology
- Physiology
Background:
- Urination is a complex physiological process controlled by central neural circuits.
- The periaqueductal gray (PAG) is a known control center for urination, but specific neuron types involved are not well-defined.
Purpose of the Study:
- To identify specific neuronal subtypes within the lateral and ventrolateral PAG (l/vlPAG) that regulate the process of urination.
- To elucidate the neural pathways involved in micturition control originating from the l/vlPAG.
Main Methods:
- Identification of somatostatin (SST)-expressing neurons in the l/vlPAG.
- Recording neuronal activity in freely moving animals during urination.
- Optogenetic activation and inhibition of SST-expressing neurons.
- Investigating projections to the pontine micturition center (PMC) and effects after pelvic nerve transection.
Main Results:
- SST-expressing neurons in the l/vlPAG showed activity correlated with urination onset.
- Optogenetic activation of these neurons induced urination and bladder contraction.
- Inhibition of these neurons suppressed ongoing urination.
- Activation of l/vlPAG SST+ neurons projecting to the PMC triggered urination, an effect dependent on the pelvic nerve.
Conclusions:
- l/vlPAG SST-expressing neurons are critical regulators of urination.
- These neurons control micturition via the PAG-PMC pathway.
- This study offers new insights into bladder control mechanisms and potential therapeutic targets for urinary dysfunction.
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