Electrical properties of neurons in the intact rat major pelvic ganglion

Tan, Hongjing; Mawe, Gary M.; Vizzard, Margaret A.

doi:10.1016/j.autneu.2007.01.013

Cited by 10 publications

(3 citation statements)

References 30 publications

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“…The most critical aspects of the protocol are correct identification of each major nerve and the complete removal of MPG tissue. With careful viewing and handling of the tissues, MPG tissues can be removed for anatomical, molecular and electrophysiological in vitro studies 18,19,20,21,22 .…”

Section: Discussionmentioning

confidence: 99%

Dissection of Pelvic Autonomic Ganglia and Associated Nerves in Male and Female Rats

Bertrand

Keast

2020

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The bilateral major pelvic ganglia (MPG; synonym, pelvic ganglia) are the primary source of postganglionic sympathetic and parasympathetic neurons innervating pelvic organs of rodents; the functionally equivalent structure in humans is the inferior hypogastric plexus. The major pelvic ganglia also provide the route by which lumbar and sacral sensory axons reach the pelvic organs. These complex, mixed ganglia can prove challenging to identify and dissect for further experimental study of normal autonomic mechanisms or to establish preclinical models of disease, injury or visceral pain. Here we describe a protocol to access and visualize these ganglia and their associated nerve tracts. We provide this protocol with schematics for both male and female rats, as the ganglion size and landmarks for identification differ between sexes. The protocol describes removal of the ganglion for in vitro studies, but this method can be integrated into a surgical recovery protocol for experimental interventions (e.g., nerve crush, nerve resection) or for mapping neuronal circuits (e.g., by microinjection of neural tracers). We also demonstrate the primary structures of the ganglion and its associated nerves immediately following dissection and following immunohistochemical staining.

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Section: Discussionmentioning

confidence: 99%

Dissection of Pelvic Autonomic Ganglia and Associated Nerves in Male and Female Rats

Bertrand

Keast

2020

JoVE

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“…The postganglionic axons from the pelvic ganglion synapse onto neurons on the bladder detrusor and urethral smooth muscles, releasing acetylcholine from parasympathetic axons and noradrenaline from sympathetic axons (Langworthy, 1965;Keast, 1995;de Groat & Yoshimura, 2015). Majority of sympathetic neurons in the ganglia express tyrosine hydroxylase (TH) and parasympathetic neurons express choline acetyltransferase(ChAT), the biosynthetic enzyme that converts choline precursor to acetylcholine (Tan et al, 2007). Synaptic transmission at the MPG neurons is mediated by acetylcholine acting on nicotinic receptors although other neurotransmitters could modulate the transmission (Dail et al, 1975;de Groat & Saum 1976;de Groat & Yoshimura, 2015;Papka et al, 1999;de Groat & Yoshimura, 2015).…”

Section: Morphological and Physiological Properties Of Major Pelvic Gangliamentioning

confidence: 99%

“…Characterization of mouse and rat MPG showed that there are mainly two types of neurons-phasic and tonic spiking neurons according to their discharge characteristics in response to depolarizing current pulses (Tan et al, 2007;Jobling & Lim, 2008).…”

Section: Morphological and Physiological Properties Of Major Pelvic Gangliamentioning

confidence: 99%

Plasticity of neurons in mouse major pelvic ganglia in response to loos of physiological input in cases of nerve injury and spinal cord injury

Kyi¹

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Autonomic dysfunctions present significant effects on day to day functions of spinal cord-injured patients. Most people with spinal cord injury (SCI) reported a desire to recover autonomic functions such as bladder and sexual functions over regaining of locomotor functions. Lower urinary tract function is one of the autonomic functions that is impaired after SCI. Acute SCI results in areflexic bladder and complete urinary retention while patients with chronic SCI suffer from hyperreflexic bladder, incontinence and inefficient voiding. While extensive SCI research has been done locomotor recovery, relatively limited amount of research has been done on the underlying mechanisms of autonomic dysfunctions associated with SCI. The major pelvic ganglia (MPG) are peripheral ganglia that consist of postganglionic neurons that innervate the urogenital organs and are a part of the neural pathway that controls micturition. In mice, there is one MPG on each side of the animal. MPG receives cholinergic parasympathetic input from the preganglionic neurons in the sacral cord through pelvic nerve and sympathetic cholinergic inputs from those in the lumbosacral cord through the hypogastric nerve. Nicotinic cholinergic transmitter system is the major system involved in ganglionic synaptic transmission at the MPG neurons. The goal of this thesis is to understand the effects of neural injury on nicotinic cholinergic transmission at the postganglionic MPG neurons that innervate the urogenital organs. We are interested in the properties of MPG neurons in these injury states because these neurons are the final neurons in the autonomic pathway that directly innervate the target organs whose functions are compromised as results of these injuries. Before we could study the state of MPG neurons in injury conditions, we first needed to characterize the properties of these neurons in uninjured physiological state. By characterizing the normal cholinergic transmission in control mice, we are able to investigate the changes in the system after injury. Secondly, we sought to understand how MPG neurons respond to abrupt loss of all synaptic inputs. In these studies, we severed all the preganglionic neurons to MPG on one side of the animals leaving the other side intact. Finally, we studied the effects spinal cord injury on the synaptic transmission at the MPG. Spinal cord injury presumably presents altered forms of presynaptic inputs from the spinal cord to the MPG neurons due to hyperreflexic nature of the reflex pathway after SCI. We utilized molecular, electrophysiological, and pharmacological approaches using mouse models to answer our questions. In the first chapter of the thesis, I characterized the synaptic, passive, and firing properties of the MPG neurons in both male and female mice. I also characterized the nicotinic acetylcholine receptor subunits involved in cholinergic neurotransmission at the MPG. In the second chapter, I studied the effects of loss of direct inputs to the MPG neurons in both ipsilateral and contralateral intact ganglia in male mice. I performed unilateral decentralization of inputs to the MPG by severing pelvic and hypogastric nerves. In the third chapter, I studied the effects of spinal cord injury on properties of presynaptic inputs to the MPG as well as postganglionic properties, passive properties and firing properties of MPG neurons. In this injury model, I performed complete transections of the spinal cords between thoracic spinal segments (T10 and T11) in both male and female mice. All the mice had impaired bladder reflexes after spinal transection. Our results showed that decentralization and spinal cord injury effect the synaptic transmission at the MPG as well as the properties of the MPG neurons differently. These effects could be due to influences from both the nature of presynaptic input and the functional state of the target organ. We also observed different effects of spinal cord injury between MPG neurons of males and female. Understanding the mechanisms of changes at the neurotransmission at MPG neurons would be important in developing therapeutic measures for autonomic dysfunctions of the urogenital organs in nerve injury or in spinal cord injury.

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The Bladder as a Dynamic System

Miftahof

Nam

2013

Biomechanics of the Human Urinary Bladder

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Electrical properties of neurons in the intact rat major pelvic ganglion

Cited by 10 publications

References 30 publications

Dissection of Pelvic Autonomic Ganglia and Associated Nerves in Male and Female Rats

Dissection of Pelvic Autonomic Ganglia and Associated Nerves in Male and Female Rats

Plasticity of neurons in mouse major pelvic ganglia in response to loos of physiological input in cases of nerve injury and spinal cord injury

The Bladder as a Dynamic System

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