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Purinergic systems receptors

Purinergic System Adenosine Receptors Sterol Transporters... [Pg.19]

Transmembrane Signaling Nicotinic Receptors Purinergic System... [Pg.661]

Purinergic System. Figure 2 Schematic of sympathetic cotransmission. ATP and NA released from small granular vesicles (SGV) act on P2X and a-i receptors on smooth muscle, respectively. ATP acting on inotropic P2X receptors evokes excitatory junction potentials (EJPs), increase in intracellular calcium ([Ca2+]j) and fast contraction while occupation of metabotropic ar-adrenoceptors leads to production of inositol triphosphate (IP3), increase in [Ca2+]j and slow contraction. Neuropeptide Y (NPY) stored in large granular vesicles (LGV) acts after release both as a prejunctional inhibitory modulator of release of ATP and NA and as a postjunctional modulatory potentiator of the actions of ATP and NA. Soluble nucleotidases are released from nerve varicosities, and are also present as ectonucleotidases. (Reproduced from Burnstock G (2007) Neurotransmission, neuromodulation cotransmission. In Squire LR (ed) New encyclopaedia of neuroscience. Elsevier, The Netherlands (In Press), with permission from Elsevier). [Pg.1051]

Purines such as ATP and adenosine play a central role in the energy metabolism of all life forms. This fact probably delayed recognition of other roles for purines as autocrine and paracrine substances and neurotransmitters. Today it is recognized that purines are released from neurons and other cells and that they produce widespread effects on multiple organ systems by binding to purinergic receptors located on the cell surface. The principal ligands for... [Pg.303]

A1 adenosine receptors are inhibitory in the central nervous system. A receptors were originally characterized on the basis of their ability to inhibit adenylyl cyclase in adipose tissue. A number of other G-protein-mediated effectors of A receptors have subsequently been discovered these include activation of K+ channels, extensively characterized in striatal neurons [13], and inhibition of Ca2+ channels, extensively characterized in dorsal root ganglion cells [14]. Activation of A receptors has been shown to produce a species-dependent stimulation or inhibition of the phosphatidylinositol pathway in cerebral cortex. In other tissues, activation of A receptors results in synergistic activation of the phosphatidylinositol pathway in concert with Ca2+-mobilizing hormones or neurotransmitters [15]. The effectors of A adenosine receptors and other purinergic receptor subtypes are summarized in Table 17-2. [Pg.313]

Bumstock, G, Overview (Purinergic receptors). In Role of adenosine and adenine nucleotides in the b/olog/col system, (eds Imai, S and Nakrtzawa, M), Elsevier Science Publishers, Amsterdam, 1991,3-16. [Pg.115]


See other pages where Purinergic systems receptors is mentioned: [Pg.243]    [Pg.657]    [Pg.1048]    [Pg.1049]    [Pg.1050]    [Pg.1052]    [Pg.1053]    [Pg.159]    [Pg.115]    [Pg.243]    [Pg.657]    [Pg.1048]    [Pg.1049]    [Pg.1050]    [Pg.1052]    [Pg.1053]    [Pg.530]    [Pg.1047]    [Pg.1052]    [Pg.306]    [Pg.1007]    [Pg.87]    [Pg.298]    [Pg.220]    [Pg.1047]    [Pg.1052]    [Pg.3111]    [Pg.153]    [Pg.60]    [Pg.20]    [Pg.22]    [Pg.24]    [Pg.126]    [Pg.271]    [Pg.37]   
See also in sourсe #XX -- [ Pg.308 , Pg.309 , Pg.310 , Pg.311 ]




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