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  4. Melatonin prevents blood vessel loss and neurological impairment induced by spinal cord injury in rats

Melatonin prevents blood vessel loss and neurological impairment induced by spinal cord injury in rats

The Journal of Spinal Cord Medicine, 2017 · DOI: 10.1080/10790268.2016.1227912 · Published: March 1, 2017

Spinal Cord InjuryEndocrinologyNeurology

Simple Explanation

This study investigates the potential protective effects of melatonin on blood vessel loss and neurological impairment following spinal cord injury (SCI) in rats. SCI often leads to progressive tissue loss due to blood vessel dysfunction and inflammation. The researchers aimed to determine if melatonin could mitigate these damages. The researchers divided rats into three groups: a sham group (no injury), an SCI group (spinal cord injury), and a melatonin group (spinal cord injury treated with melatonin). They assessed blood vessel density, blood-spinal cord barrier (BSCB) permeability, neuron count, and levels of proteins related to neurological plasticity. The study found that melatonin treatment helped rescue blood vessels, reduce BSCB permeability, increase neuron count, and partially prevent the reduction of key proteins (BDNF, synapsin I, GAP-43) associated with neurological plasticity in both the spinal cord and hippocampus. These findings suggest melatonin has a neuroprotective effect after SCI.

Study Duration
7 days post-injury
Participants
63 female Sprague-Dawley rats
Evidence Level
Not specified

Key Findings

  • 1
    Melatonin treatment rescued blood vessels, as indicated by increased CD31 levels and ameliorated BSCB permeability at 7 days post-injury.
  • 2
    Melatonin significantly increased the number of neurons and the expression of Nissl bodies in neurons at the injury epicenter.
  • 3
    SCI reduced levels of BDNF, synapsin I, and GAP-43 in the spinal cord and hippocampus, and melatonin treatment partially prevented these reductions.

Research Summary

This study investigated the neuroprotective effects of melatonin on spinal cord injury (SCI) in rats, focusing on blood vessel loss and neurological impairment. The results demonstrated that melatonin treatment rescued blood vessels, decreased blood-spinal cord barrier (BSCB) permeability, and protected neurons after SCI. Melatonin treatment also counteracted the injury-related reductions in BDNF, synapsin I, and GAP-43, emphasizing its effect on molecular systems that support neurological plasticity.

Practical Implications

Therapeutic Potential

Melatonin may be a potential therapeutic agent for mitigating blood vessel loss and neurological impairment following spinal cord injury.

Microcirculation Importance

The study highlights the importance of preserving microcirculation in the spinal cord to promote neuronal survival and neurological function after SCI.

Neurological Plasticity

Melatonin's influence on BDNF, synapsin I, and GAP-43 suggests it can support neurological plasticity and recovery after SCI.

Study Limitations

  • 1
    The molecular mechanism underlining those effects
  • 2
    The relationship between vascular preservation and neurological protection should be explored in further studies.
  • 3
    We did not investigate the effect of melatonin on angiogenesis and arteriogensis which represent important potential for treatment of vascular network.

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