Anti-nociceptive effects of non-antibiotic derivatives of demeclocycline and doxycycline against formalin-induced pain stimulation

Eur J Pharmacol. 2024 Dec 5:984:177054. doi: 10.1016/j.ejphar.2024.177054. Epub 2024 Oct 10.

Abstract

In previous studies, some tetracycline (TC) antibiotics showed potential as analgesic. We investigated here the analgesic activity of new non-antibiotic TC derivatives using the formalin-induced nociceptive pain model in adult C57BL/6 mice. Specifically, we tested the effects of i.p. injections of DDMC (5, 10, 20 mg kg-1) and DDOX (10, 20, 40 mg kg-1), which are non-antibiotic derivatives of demeclocycline and doxycycline, respectively. Repeated treatments with DDMC remarkably reduced nociceptive pain in both phases of the test, at 10 mg kg-1 its efficacy was comparable to that of 10 mg kg-1 of morphine. DDOX was also effective in this paradigm but intrinsically less potent than DDMC, exerting analgesic effects between 20 and 40 mg kg-1. Interestingly, a single injection of DDMC (10 mg kg-1) was sufficient to produce a robust anti-nociceptive effect similar to that of morphine. A single injection of DDOX (40 mg kg-1) also produced anti-nociceptive effects but only in the second phase of the test. Noticeably, male mice exhibited a better analgesic response to DDMC (10 mg kg-1) than females. A single injection of DDMC (10 mg kg-1) and morphine but not of DDOX (40 mg kg-1), powerfully inhibited formalin-induced spinal cord c-Fos expression whereas both TC derivatives restrained the activation of Iba-1-immunoreactive cells, indicating a potential indirect effect on inflamed microglial cells. In summary, the non-antibiotic TCs, DDMC and DDOX, demonstrated notable analgesic efficacy against formalin-induced pain, suggesting their potential as alternatives for analgesic treatment.

Keywords: Formalin-pain model; Microglia; Non-antibiotic tetracyclines; Pain; c-Fos.

MeSH terms

  • Analgesics* / chemistry
  • Analgesics* / pharmacology
  • Analgesics* / therapeutic use
  • Animals
  • Doxycycline* / pharmacology
  • Female
  • Formaldehyde*
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Pain / drug therapy
  • Proto-Oncogene Proteins c-fos / metabolism

Substances

  • Formaldehyde
  • Analgesics
  • Doxycycline
  • Proto-Oncogene Proteins c-fos