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  4. An immunohistochemical study on the presence of nitric oxide synthase isoforms (nNOS, iNOS, eNOS) in the spinal cord and nodose ganglion of rats receiving ionising gamma radiation to their liver

An immunohistochemical study on the presence of nitric oxide synthase isoforms (nNOS, iNOS, eNOS) in the spinal cord and nodose ganglion of rats receiving ionising gamma radiation to their liver

J Vet Res, 2020 · DOI: 10.2478/jvetres-2020-0059 · Published: January 1, 2020

OncologyNeurologyVeterinary Medicine

Simple Explanation

This study investigates how exposing the liver to radiation affects the presence of certain substances (nitric oxide synthase isoforms) in the spinal cord and a specific nerve cluster called the nodose ganglion in rats. Rats were exposed to radiation, and then researchers looked at the spinal cord and nodose ganglion to see where and how much of these substances were present using a special staining technique. The study found that radiation does change the presence of these substances, suggesting a connection between liver damage from radiation and changes in the nervous system.

Study Duration
3 Days
Participants
32 male rats
Evidence Level
Not specified

Key Findings

  • 1
    nNOS immunoreactivity was found in the superficial lamina (lamina I–II) of the spinal cord of the rats with ionising radiation insult to the liver, and to a lesser extent in lamina III–IV.
  • 2
    Inducible NOS was intensely stained in the ependymal cells of the spinal cord from the first day, and this staining weakened day by day.
  • 3
    In the nodose ganglion, mild diffuse cytoplasmic staining in neurons on the first day, intense local cytoplasmic staining on the second day, and nuclear staining on the third day were determined for eNOS.

Research Summary

This study determined the presence of nitric oxide synthesis isoforms (nNOS, iNOS, and eNOS) in thoracic spinal cord segments and nodose ganglia of rats with gamma-irradiated livers. The nNOS, iNOS, and eNOS isoforms are activated in the spinal cord and nodose ganglion of rats after ionising radiation insult to the liver. It was observed that three NOS isoforms (nNOS, iNOS, and eNOS) were activated in the spinal cord and nodose ganglion of rats treated with ionising radiation to the liver, and that this occurred in different cells (neuronal cells, neuroglia cells, and vascular endothelial cells) of the nervous system.

Practical Implications

Understanding Pain Mechanisms

The study provides insights into how radiation-induced liver damage may lead to pain through the activation of NOS isoforms in the spinal cord and nodose ganglion.

Neuroprotective Strategies

The findings could contribute to the development of neuroprotective strategies to mitigate the neurological effects of radiation therapy.

Targeted Therapies

Identifying specific NOS isoforms involved in radiation-induced neurological changes may lead to targeted therapies to alleviate symptoms.

Study Limitations

  • 1
    The study was conducted on rats, and the results may not be directly applicable to humans.
  • 2
    The study only examined the effects of a single dose of radiation.
  • 3
    Further studies are needed to elucidate the specific mechanisms by which NOS isoforms are activated in the spinal cord and nodose ganglion after radiation exposure.

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