(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.