ライフサイエンスコーパス: cotransmitter

1 ptically by neuropeptide Y (NPY), an adrenal cotransmitter.

2 he ventral tegmental area use glutamate as a cotransmitter.

3 smitter and others defining it as a neuronal cotransmitter.

4 ns, including those with overlapping sets of cotransmitters.

5 are both neurotransmitters that interact as cotransmitters.

6 circuit that uses GABA and dopamine (DA) as cotransmitters.

7 uivocally that these peptides are functional cotransmitters.

8 tides contained in neuron B15 are functional cotransmitters.

9 emporal disparity in the overflow of the two cotransmitters.

10 results indicate that evoked overflow of the cotransmitters accurately reflects release from nerves.

11 In summary, cotransmitters acting on different network targets act c

12 ting a spatial and functional segregation of cotransmitter actions.

13 asticity requires neuropeptide Y, an adrenal cotransmitter and the activation of adrenal Y5 receptors

14 c combinations of GABA and neuropeptide Y as cotransmitters and Lim1,2 and Nurr1 transcription factor

15 hese neurons contains a unique complement of cotransmitters and that each of these neurons elicits a

16 ceptors, block sympathetic release of NA and cotransmitters, and act as control, respectively.

17 To unequivocally assign neurotransmitters, cotransmitters, and neuromodulators to identified classe

18 of release from nerves suggests that the two cotransmitters are released from two separate population

19 C2 is thought to use histamine and NO as cotransmitters at this synapse, because both agents mimi

20 nfluence via bath application of the peptide cotransmitter Cancer borealis tachykinin-related peptide

21 e rhythmic movements illustrates the role of cotransmitter complement in motor pattern selection and

22 tion of strategies, including using distinct cotransmitter complements, to elicit different outputs f

23 is often attributed to their having distinct cotransmitter complements.

24 gene in the mouse reduced chromaffin granule cotransmitter concentrations by approximately 40-80%.

25 ifferent projection neurons may use the same cotransmitters differently to elicit distinct pyloric rh

26 receptors, the findings establish zinc as a cotransmitter during physiological signalling at the mos

27 sion, plasticity and differential control of cotransmitter expression.

28 he developmental acquisition of three of the cotransmitters found in the gastropyloric receptor (GPR)

29 ors in three different pain conditions--as a cotransmitter from sympathetic nerves in causalgia and r

30 The cotransmitter histamine induces essentially the same mem

31 nalling molecule that has been retained as a cotransmitter in every nerve type in both peripheral and

32 lanin is a stress-inducible neuropeptide and cotransmitter in serotonin and norepinephrine neurons wi

33 is nervous control of the heart by ATP as a cotransmitter in sympathetic, parasympathetic, and senso

34 pelling evidence that glutamate can act as a cotransmitter in the mammalian brain.

35 pears to function as an "emergency response" cotransmitter in the sympathoadrenal axis, where the pri

36 Many neurons contain multiple peptide cotransmitters in addition to their classical transmitte

37 hors concluded that ENK and glutamate may be cotransmitters in LC afferents.

38 Acetylcholine and ATP are excitatory cotransmitters in parasympathetic nerves.

39 ators can be delivered as local hormones, as cotransmitters in projection neurons, and through the ge

40 s and facilitation of the release of peptide cotransmitters in these interneurons.

41 Neuropeptide Y (NPY), a sympathetic cotransmitter, is the most abundant peptide in the heart

42 non and suggests that the release of peptide cotransmitters may exhibit similar types of regulation a

43 ting that BH(4) acts through adrenergic, not cotransmitter, mechanisms.

44 n be orchestrated via recruitment of peptide cotransmitter neurons.

45 Further, we identified cotransmitters of histaminergic neurons in the ventrocau

46 hat there is a sequential acquisition of the cotransmitters of the GPR neurons.

47 neurons, allatotropin and TKRPs might act as cotransmitters or neuromodulators.

48 ty of substances that can potentially act as cotransmitters or neuromodulators.

49 e due to differences in the clearance of the cotransmitters or to the release of purines from non-neu

50 nal identity features of a neuron, including cotransmitter phenotypes.

51 Because these cotransmitters regulate an aspect of muscle contractions

52 The net effect of the modulatory peptide cotransmitters released from motorneuron B16 would be to

53 jects is mediated by both NA and sympathetic cotransmitter(s); however, reflex VC in aged skin is att

54 background K(+) currents or activation by a cotransmitter, serotonin.

55 ons, that differentially express the peptide cotransmitter, somatostatin.

56 lly considered to act as neuromodulators and cotransmitters that modify the effect of "classical" tra

57 ansmitter but also contains putative peptide cotransmitters, the small cardioactive peptides (SCPs) a

58 utions of noradrenaline (NA) and sympathetic cotransmitters to reflex-mediated cutaneous VC are alter

59 ow any individual projection neuron uses its cotransmitters to select a motor pattern.

60 strongly suggest that CART peptides may be a cotransmitter with GABA in a subpopulation of projection

61 ase glutamate and gamma-aminobutyric acid as cotransmitters, with striking regional variation.