Technical note demonstrates solid-phase microextraction advantages for nicotine metabolite analysis in rat brain, suggesting valuable insights for biomedicine.
Nicotine's neuroactive properties and influence on brain metabolism are not widely explored, particularly in spatially resolved contexts. This technical note presents an in vivo solid-phase microextraction method coupled with UHPLC-TOF/MS to investigate the temporo-spatial distribution of nicotine-associated metabolites in rat brain regions. The coating material, a Palladium-doped covalent organic framework (I-TFBPT-COF@Pd), exhibited a large surface area, suitable pore diameter, and good biocompatibility. The metabolite distribution pattern spectra demonstrated SPME's superior adsorption performance, as evidenced by a broader and more uniform distribution of metabolites. Principal component analysis and orthogonal partial least-squares discriminant analysis indicated that nicotine exposure induced a profound alteration in the metabolite composition of the experimental samples. In addition, 46 differential metabolites and 7 key pathways in the hippocampus and striatum were identified, which revealed the range of nicotine's influence on various biochemical processes, including neurotransmitter synthesis, energy metabolism, and inflammation regulation. This method provides an effective way to study the potential neural effects of nicotine in the brain, surpassing traditional sampling techniques, and it has broad application prospects in biomedicine.
No takes yet. Share an insight, caveat, or question.
Zhang et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: