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  4. Beyond the lesion site: minocycline augments inflammation and anxiety-like behavior following SCI in rats through action on the gut microbiota

Beyond the lesion site: minocycline augments inflammation and anxiety-like behavior following SCI in rats through action on the gut microbiota

Journal of Neuroinflammation, 2021 · DOI: https://doi.org/10.1186/s12974-021-02123-0 · Published: May 7, 2021

Spinal Cord InjuryImmunologyGastroenterology

Simple Explanation

This study investigates how minocycline, a drug with anti-inflammatory and antibiotic effects, impacts the gut microbiota and immune response after spinal cord injury (SCI) in rats. The researchers examined how minocycline affects the connection between the gut microbiota and immune system, and whether it influences motor recovery and anxiety-like behavior. The researchers found that minocycline significantly altered the gut microbiota composition and diversity in the rats. This change in the gut was linked to a normalization of SCI-induced suppression of cytokines and chemokines, which are important for immune signaling. The study also observed that minocycline reduced anxiety-like behavior, which is often linked to gut dysbiosis after SCI. The study concludes that minocycline's effects on the gut microbiota occur before its long-term effects on the systemic immune system following SCI. This suggests that the gut microbiota could be a key target for minocycline's therapeutic effects in central nervous system diseases and injuries.

Study Duration
4 weeks
Participants
36 female Lewis rats
Evidence Level
Not specified

Key Findings

  • 1
    Minocycline had a profound acute effect on the microbiota diversity and composition, which was paralleled by the subsequent normalization of spinal cord injury-induced suppression of cytokines/chemokines.
  • 2
    Minocycline attenuated spinal cord injury-induced microglial activation, it did not affect the lesion size or promote measurable motor recovery.
  • 3
    Minocycline treatment had a long-term (i.e., at least 2 weeks after the offset of treatment) attenuation of anxiety-like behavior in the LDB but did not promote motor recovery following SCI.

Research Summary

The study aimed to elucidate the system-wide changes induced by minocycline treatment in a rodent model of cervical SCI, focusing on the microbiota-immune axis and behavioral outcomes. Minocycline treatment for SCI has a profound acute effect on the fecal microbiota diversity and composition and subsequently prevents SCI-induced suppression of cytokines/chemokines and attenuates anxiety-like behaviors. Minocycline's impact on the intestinal microbiota may also affect the systemic immune and affective consequences of SCI. Changes in plasma cytokine/chemokine levels were preceded by minocycline-induced changes in the fecal microbiota composition.

Practical Implications

Therapeutic Target Identification

The gut microbiota may be a key target for minocycline's therapeutic effects in central nervous system diseases and injuries.

Understanding SCI Complications

Highlights the importance of the microbiota-immune axis for recovery following SCI, especially when considering treatments that may modulate this axis.

Clinical Application of Minocycline

Provides a comprehensive understanding of the full spectrum of minocycline activity beyond the lesion site, relevant for potential clinical application of minocycline to treat acute SCI in humans.

Study Limitations

  • 1
    The utilized motor tests in the present study may not have been sensitive enough to detect changes in fine motor skills.
  • 2
    The present results are descriptive in nature.
  • 3
    Given the sex differences in immune response, this study should be repeated in male rats.

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