Hydrogen Therapy Protects Spinal Cord from Injury in Animal Study

Authors
Journal
Pharmaceuticals
Year
DOI
10.3390/ph16040527
Study Type
Rat
Outcome
Positive
Peer Reviewed
Yes
Country
Turkey
Health Condition
Spinal Cord Injury
Body System
Nervous System

TL;DR

Hydrogen-rich saline (HRS) reduces inflammation and cell death in rats with spinal cord injuries.

Key Finding

Hydrogen-rich saline reduced inflammatory markers (IL-6 and TNF-α) and decreased cell death in rat spinal cord tissue after injury.

Summary

Researchers tested whether hydrogen-rich saline (a salt solution containing dissolved hydrogen) could protect rat spinal cords from injury. After injuring the spinal cords of rats, they gave some animals hydrogen-rich saline injections for a week. The treated rats showed lower levels of inflammatory chemicals (IL-6 and TNF-α) in their blood and less cell death in the damaged spinal tissue compared to injured rats that received no treatment.

Practical Takeaway

This is early-stage animal research showing hydrogen-rich saline may have protective effects on spinal cord damage. However, this study was conducted only in rats, so results cannot be directly applied to humans. Much more research, including human trials, would be needed before any health recommendations could be made.

Abstract

The anti-inflammatory and anti-apoptotic effects of molecular hydrogen, delivered as hydrogen-rich saline (HRS), on spinal cord injury was investigated. Four-month-old male Sprague Dawley rats (n = 24) were classified into four groups: (1) control-laminectomy only at T7-T10; (2) spinal injury-dura left intact, Tator and Rivlin clip compression model applied to the spinal cord for 1 min, no treatment given; (3) HRS group-applied intraperitoneally (i.p.) for seven days; and (4) spinal injury-HRS administered i.p. for seven days after laminectomy at T7-T10 level, leaving the dura intact and applying the Tator and Rivlin clip compression model to the spinal cord for 1 min. Levels of interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α) were measured in blood taken at day seven from all groups, and hematoxylin-eosin (H & E) and terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) were used to stain the tissue samples. IL-6 and TNF-α levels were significantly lower in the group treated with HRS following the spinal cord injury compared to the group whose spinal cord was damaged. A decrease in apoptosis was also observed. The anti-inflammatory and anti-apoptotic effect of IL-6 may be a clinically useful adjuvant therapy after spinal cord injury.