AI Article Synopsis

  • The study investigated the impact of 7-day exposure to multifunctional enkephalin analogs on protein composition in rat spleen lymphocytes, brain cortex, and hippocampus at doses of 3 mg/kg and 10 mg/kg.
  • Proteomic analysis revealed significant changes in protein expression in these areas, particularly with the 3 mg/kg dose showing effects on RNA processing and cytoskeletal dynamics.
  • The 10 mg/kg dose caused extensive modifications in spleen lymphocytes, increasing proteins related to immune responses and apoptosis, while also altering protein expression in the brain regions related to transcription regulation and neuronal plasticity.

Article Abstract

This work aimed to test the effect of 7-day exposure of rats to multifunctional enkephalin analogs and at doses of 3 mg/kg and 10 mg/kg on the protein composition of rat spleen lymphocytes, brain cortex, and hippocampus. Alterations of proteome induced by and were compared with those elicited by morphine. The changes in rat proteome profiles were analyzed by label-free quantification (MaxLFQ). Proteomic analysis indicated that the treatment with 3 mg/kg of caused significant alterations in protein expression levels in spleen lymphocytes (45), rat brain cortex (31), and hippocampus (42). The identified proteins were primarily involved in RNA processing and the regulation of cytoskeletal dynamics. In spleen lymphocytes, the administration of the higher 10 mg/kg dose of both enkephalin analogs caused major, extensive modifications in protein expression levels: (119) and (182). Among these changes, the number of proteins associated with immune responses and apoptotic processes was increased. treatment resulted in the highest number of alterations in the rat brain cortex (152) and hippocampus (45). The altered proteins were functionally related to the regulation of transcription and cytoskeletal reorganization, which plays an essential role in neuronal plasticity. Administration with did not increase the number of altered proteins in the brain cortex (26) and hippocampus (26). Our findings demonstrate that the effect of κ-OR full antagonism of is opposite in the central nervous system and the peripheral region (spleen lymphocytes).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406115PMC
http://dx.doi.org/10.3390/biomedicines10081969DOI Listing

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