AI Article Synopsis

  • The study aimed to investigate how oxymatrine (OMT) affects N-type voltage-gated calcium channels (VGCCs) and their role in pain management in mice.
  • Researchers divided 45 mice into three groups to analyze changes in intracellular calcium levels and protein expression of N-type and L-type VGCCs after partial sciatic nerve ligation and OMT treatment.
  • Results showed that OMT treatment reduced calcium levels and altered N-type VGCC protein expression, suggesting that its analgesic effects are linked to modifications in the Cav2.2 channel's activity.

Article Abstract

Objective: To study whether the analgesis of oxymatrine (OMT) affects N-type voltage-gated calcium channels (VGCCs).

Methods: Totally 45 mice were randomly divided into the sham-operation group, the model group [established by partial sciatic nerve ligation (PSNL)] , and the OMT treatment group according to random digit table, 15 in each group. The dorsal root ganglions (DRG) were separated in PSNL pain model mice. Intracellular calcium concentration ([Ca2+]i) was determined with Fluo-3 AM immunofluorescent probe in cultured DRG neurons. Different protein expression levels of N-type (Cav2. 2) and L-type ( Cav1. 3) among VGCCs from brain and DRG tissues were detected with Western blot.

Results: Compared with the sham-operation group, [Ca2+]i, increased in cultured DRG neurons (P <0. 05) , protein expression levels of Cav2. 2 in the brain tissue increased (P <0. 05), protein expression levels of Cav2. 2 in DRG tissues decreased in the model group (P <0. 01). Compared with the model group, [Ca2+]i, decreased in cultured DRG neurons (P < 0. 05), protein expression levels of Cav2. 2 in the brain tissue decreased (P <0. 01), protein expression levels of Cav2. 2 in DRG tissues increased in the OMT treatment group (P <0. 01). There was no statistical difference in Cav1. 3 expressions in cultured DRG neurons and the brain (P >0. 05).

Conclusion: Analgesic effect of OMT might be related to Cav2. 2 channel mediated calcium ion flux.

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