Blood oxygen regulation via P2Y12R expressed in the carotid body

Iring, András ✉ [Iring, András (Élettan), szerző] Transzlációs Medicina Intézet (SE / AOK / I); Molekuláris Farmakológia Kutatócsoport (HRN KOKI); Baranyi, Mária [Baranyi, Mária (Molekuláris farma...), szerző] Molekuláris Farmakológia Kutatócsoport (HRN KOKI); Iring‑Varga, Bernadett [Varga, Bernadett (funkcionális ideg...), szerző] Doktori Iskola (SE); Molekuláris Farmakológia Kutatócsoport (HRN KOKI); Mut‑Arbona, Paula [Mut-Arbona, Paula (Neuroscience), szerző] Doktori Iskola (SE); Molekuláris Farmakológia Kutatócsoport (HRN KOKI); Gál, Zsuzsanna T. [Gál, Zsuzsanna Tamara (Neurobiológia, Ne...), szerző] Molekuláris Farmakológia Kutatócsoport (HRN KOKI); Nagy, Dorina [Nagy, Dorina (Élettan), szerző] Transzlációs Medicina Intézet (SE / AOK / I); HUN-REN-SE Cerebrovaszkuláris és Neurokognitív ... (SE / AOK / I / TMI); Hricisák, László [Hricisák, László (Humán élettan), szerző] Transzlációs Medicina Intézet (SE / AOK / I); HUN-REN-SE Cerebrovaszkuláris és Neurokognitív ... (SE / AOK / I / TMI); Varga, János [Varga, János Tamás (pulmonológia, pul...), szerző] Pulmonológiai Klinika (SE / AOK / K); Benyó, Zoltán [Benyó, Zoltán (Élettan és kóréle...), szerző] Transzlációs Medicina Intézet (SE / AOK / I); HUN-REN-SE Cerebrovaszkuláris és Neurokognitív ... (SE / AOK / I / TMI); Sperlágh, Beáta [Sperlágh, Beáta (Neurofarmakológia), szerző] Doktori Iskola (SE); Molekuláris Farmakológia Kutatócsoport (HRN KOKI)

Angol nyelvű Szakcikk (Folyóiratcikk) Tudományos
Megjelent: RESPIRATORY RESEARCH 1465-9921 1465-993X 25 (1) Paper: 61 , 20 p. 2024
  • SJR Scopus - Pulmonary and Respiratory Medicine: Q1
Azonosítók
Támogatások:
  • (Hungarian Research and Development Fund [Grant Number 3162931629) Támogató: NKFI
  • (Hungarian Research and Development Fund [Grant Number 125174) Támogató: NKFI
  • (Hungarian Research and Development Fund [Grant Number 139230) Támogató: NKFI
  • Hungarian Brain Research Program(2017-1.2.1-NKP-2017-00002) Támogató: NKFIH
  • Recovery and Resilience Facility of the European Union within the framework of Program Széchenyi ...(RRF-2.3.1-21-2022-00011)
  • National Laboratory of Translational Neuroscience (TINL)(RRF-2.3.1-21-2022-00011)
  • Recovery and Resilience Facility of the European Union within the framework of Programme Szécheny...(RRF-2.3.1-21-2022-00011)
  • (RRF-2.3.1-21-2022-00011)
  • National Laboratory of Translational Neuroscience(RRF-2.3.1-21-2022-00015)
  • Nemzeti Gyógyszerkutatási és Fejlesztési Laboratórium (PharmaLab)(RRF-2.3.1-21-2022-00015) Támogató: NKFIH
  • PharmaLab(RRF-2.3.21-2022-00015) Támogató: NKFIH
  • (PC-II-2/2022) Támogató: Hungarian Academy of Sciences
  • Hungarian Academy of Sciences Premium Postdoctoral Research Program(PPD2019-20/2019-439)
Background: Peripheral blood oxygen monitoring via chemoreceptors in the carotid body (CB) is an integral function of the autonomic cardiorespiratory regulation. The presence of the purinergic P2Y12 receptor (P2Y12R) has been implicated in CB; however, the exact role of the receptor in O2 sensing and signal transduction is unknown. Methods: The presence of P2Y12R was established by immunoblotting, RT qPCR and immunohistochemistry. Primary glomus cells were used to assess P2Y12R function during hypoxia and hypercapnia, where monoamines were measured by HPLC; calcium signal was recorded utilizing OGB-1 and N-STORM Super-Resolution System. Ingravescent hypoxia model was tested in anaesthetized mice of mixed gender and cardiorespiratory parameters were recorded in control and receptor-deficient or drug-treated experimental animals. Results: Initially, the expression of P2Y12R in adult murine CB was confirmed. Hypoxia induced a P2Y12R-dependent release of monoamine transmitters from isolated CB cells. Receptor activation with the endogenous ligand ADP promoted release of neurotransmitters under normoxic conditions, while blockade disrupted the amplitude and duration of the intracellular calcium concentration. In anaesthetised mice, blockade of P2Y12R expressed in the CB abrogated the initiation of compensatory cardiorespiratory changes in hypoxic environment, while centrally inhibited receptors (i.e. microglial receptors) or receptor-deficiency induced by platelet depletion had limited influence on the physiological adjustment to hypoxia. Conclusions: Peripheral P2Y12R inhibition interfere with the complex mechanisms of acute oxygen sensing by influencing the calcium signalling and the release of neurotransmitter molecules to evoke compensatory response to hypoxia. Prospectively, the irreversible blockade of glomic receptors by anti-platelet drugs targeting P2Y12Rs, propose a potential, formerly unrecognized side-effect to anti-platelet medications in patients with pulmonary morbidities.
Hivatkozás stílusok: IEEEACMAPAChicagoHarvardCSLMásolásNyomtatás
2025-04-27 19:55