ライフサイエンスコーパス: parasympathetic nerve

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1 is caused by the release of ATP and ACh from parasympathetic nerves.

2 ine and ATP are excitatory cotransmitters in parasympathetic nerves.

3 ized rats after bilateral transection of the parasympathetic nerves.

4 ll secretion in vivo is under the control of parasympathetic nerves.

5 pathetic nerves induce a greater effect than parasympathetic nerves.

6 erve to oppose airway contraction induced by parasympathetic nerve activation in the airways.

7 ollowing pharmacological blockade of cardiac parasympathetic nerve activity in eight young subjects,

8 ectrophysiological recordings showed reduced parasympathetic nerve activity in the basal state and no

9 derstand how known age-related reductions in parasympathetic nerve activity influence CBR response la

10 rves innervating the larynx can alter airway parasympathetic nerve activity, transection of the super

11 The following conclusions were drawn: parasympathetic nerves and M(1), M(2), and M(3) muscarin

12 at renal afferents travel in sympathetic and parasympathetic nerves and that this information may con

13 mplementary signals derived from beta-cells, parasympathetic nerves, and increased islet blood flow.

14 Parasympathetic nerves are a vital component of the prog

15 This suggests that parasympathetic nerves are capable of re-innervating an

16 tissue was essentially devoid of sensory and parasympathetic nerves at all time points.

17 stent with a pathway where VIP released from parasympathetic nerves binds to VIPRs types I and II, ac

18 protein released from eosinophils to airway parasympathetic nerves blocks inhibitory M(2) muscarinic

19 bitory M2 muscarinic receptors on the airway parasympathetic nerves causes vagally mediated bronchoco

20 atory nucleus, which activates tarsal muscle parasympathetic nerves, elicited large contractions at 2

21 Inhibitory M2 muscarinic receptors on parasympathetic nerve endings in the lungs decrease rele

22 of inhibitory M2 muscarinic receptors on the parasympathetic nerve endings is likely to contribute to

23 vealed that the densities of sympathetic and parasympathetic nerve fibers in tumor and surrounding no

24 lex arrangement of sensory, sympathetic, and parasympathetic nerve fibers that contain classical tran

25 ered to the epicardial fat pad that projects parasympathetic nerve fibers to the AVN in 12 dogs durin

26 We propose that neurturin will protect the parasympathetic nerves from damage and improve organ reg

27 Parasympathetic nerves from the pterygopalatine ganglia

28 is mediated in part through the influence of parasympathetic nerves from the pterygopalatine ganglia.

29 demonstrate an unexpected role for SOX2 and parasympathetic nerves in generating the acinar lineage

30 The goal of this study was to determine if parasympathetic nerves in the anterior fat pad (FP) can

31 of inhibitory M2 muscarinic autoreceptors on parasympathetic nerves in the lung, potentiating vagally

32 of inhibitory M2 muscarinic autoreceptors on parasympathetic nerves in the lungs, and airway hyperres

33 inhibitory M(2) muscarinic receptors on the parasympathetic nerves, increasing acetylcholine release

34 holinergic and nonadrenergic, noncholinergic parasympathetic nerves innervating the airways are subje

35 It may be concluded that the parasympathetic nerves innervating the cerebral circulat

36 active intestinal peptide (VIP), secreted by parasympathetic nerves, is a surprising player in direct

37 inhibitory M2 muscarinic receptors (M2Rs) on parasympathetic nerves limit acetylcholine release.

38 muscarinic receptors (M(2)Rs) on the airway parasympathetic nerves limit acetylcholine release.

39 addressed the hypothesis that noncholinergic parasympathetic nerves modulate airway smooth-muscle (AS

40 These results show that noncholinergic parasympathetic nerves modulate ASM tone.

41 suggest that nitric oxide (NO) released from parasympathetic nerves participates in vasodilatation of

42 exly activated by bradykinin, noncholinergic parasympathetic nerves partly reversed histamine-induced

43 Here, we demonstrate that parasympathetic nerves regulate tubulogenesis in the dev

44 indicate that cholinergic and noncholinergic parasympathetic nerves regulating airway caliber in guin

45 active intestinal polypeptide-immunoreactive parasympathetic nerves revealed fibers associated predom

46 ceptor-mediated prejunctional enhancement of parasympathetic nerve-smooth muscle neurotransmission, w

47 The influence of sympathetic and parasympathetic nerve stimulations on salivary secretion

48 classical' transmitters from sympathetic and parasympathetic nerves supplying various peripheral targ

49 Transvascular atrial parasympathetic nerve system modification by RFCA abolis

50 are triggered by stochastic ATP release from parasympathetic nerve terminals rather than being myogen

51 ce of ACh was sympathetic nerves rather than parasympathetic nerves that are the normal source of ACh

52 d airway hyperreactivity are mediated by the parasympathetic nerves that release acetylcholine onto m

53 ctrical field stimulation was used to excite parasympathetic nerves to increase action potentials, Ca

54 n, including 'hardwiring' of sympathetic and parasympathetic nerves to lymphoid organs.

55 asma glucose = 1.9 +/- 0.1 mmol/l) activated parasympathetic nerves to the pancreas as assessed by in

56 er smooth muscle contraction is triggered by parasympathetic nerves, which release ATP and acetylchol

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