ライフサイエンスコーパス: allatostatin

1 or output induced by the neuropeptide C-type allatostatin.

2 silenced by application of an insect peptide allatostatin.

3 We find that the enteric peptide Allatostatin A (AstA) enhances wakefulness, and during i

4 endocrine cells) expressing the neuropeptide allatostatin A (AstA) inhibits or limits several starvat

5 We suggest the neuropeptide families allatostatin A (AstA), allatotropin (AT), short neuropep

6 dy demonstrates that the insect neuropeptide allatostatin A and its receptor AstAR1 activate a neuroe

7 Janu-AstA signals with the neuropeptide Allatostatin A to promote water seeking and to inhibit f

8 ed into three different types in arthropods: allatostatin A, allatostatin B, allatostatin C.

9 Allatostatin A, allatotropin, SIFamide, FMRFamide-relate

10 signed to products of 10 neuropeptide genes (allatostatins A, B, C, SIFamide, allatotropin, FMRFamide

11 cal response-properties to dopamine (DA) and allatostatin-A (AstA) in response to different types of

12 the prepropeptides for corazonin, kinin, and allatostatin-A.

13 Application of the receptor's ligand, allatostatin (AL), leads to a dramatic reduction in neur

14 ted] after application of its peptide ligand allatostatin (AL).

15 10 peptide families, including the RFamide, allatostatin, and orcokinin families.

16 Allatostatins are neuropeptides in arthropods that inhib

17 Allatostatins are pleiotropic neuropeptides for which on

18 Among these are the allatostatin (AST) B types, also known as myoinhibitory

19 fferent types in arthropods: allatostatin A, allatostatin B, allatostatin C.

20 bombesin receptors, responds specifically to allatostatin B.

21 ere we show that myoinhibitory peptide (MIP)/allatostatin-B, a pleiotropic neuropeptide widespread am

22 e raised an antibody against Cancer borealis allatostatin-B1 (CbAST-B1; VPNDWAHFRGSWa) and used it to

23 neurons (DN3s) that express the neuropeptide allatostatin C (AstC) facilitates recovery from cold-ind

24 Allatostatin C (AstC) was first isolated from Manduca se

25 press a nociception-suppressing neuropeptide Allatostatin C (AstC), which is related to a mammalian a

26 razonin (CG10698), dFMRF-amide (CG2114), and allatostatin C (CG7285 and CG13702).

27 We then cloned two putative allatostatin C-like receptors and through NCBI Conserved

28 arthropods: allatostatin A, allatostatin B, allatostatin C.

29 Aedes aegypti PISCF-allatostatin or allatostatin-C (Ae-AS-C) was isolated using a combinatio

30 Somatostatin (SS) and allatostatin-C (ASTC) are inhibitory neuropeptides in ch

31 Our previous mRNA profiling suggested that Allatostatin-C (AstC) is an eighth neuropeptide and spec

32 Here, we have identified the neuropeptide allatostatin-C (AstC)-producing neurons that gate both t

33 th one population inhibiting feeding through allatostatin-C and the other promoting courtship through

34 licing variants of three neuropeptide genes (allatostatin CC, CCHamide 1, and short neuropeptide F) a

35 These peptides include allatostatins, crustacean cardioactive peptide (CCAP), c

36 The neuropeptide allatostatin decreases the spike rate in response to tim

37 ng with antisera against Diploptera punctata allatostatin (Dip-AST), Manduca sexta allatotropin (Mas-

38 ated transfected neurons with the Drosophila allatostatin G protein-coupled receptor (AlstR)/ligand s

39 , also labeled with an antiserum against Dip-allatostatin I.

40 a new beta-PDH isoform and the first B-type allatostatins identified from a non-insect species).

41 Three types of allatostatins in insects have been isolated: FGLamides,

42 e learned in order to understand the role of allatostatins in the modulation of hormone production.

43 afferents of this receptor demonstrate that allatostatin increases the conductance of the neurons, c

44 d H. gammarus, all of the serotonin-like and allatostatin-like immunoreactivity colocalizes in neurop

45 Allatostatin-like immunoreactivity was visible first in

46 examined the distribution of serotonin-like, allatostatin-like, and FLRF(NH2)-like immunoreactivities

47 neurons of the adult contain serotonin-like, allatostatin-like, and Phe-Leu-Arg-Phe-amide (FLRF(NH2))

48 ; the remaining five families are related to allatostatin, myomodulin, buccalin/drosulfakinin, orcoki

49 us system of various insects and include the allatostatins of cockroaches and crickets, the schistost

50 Aedes aegypti PISCF-allatostatin or allatostatin-C (Ae-AS-C) was isolated us

51 rent populations of neighboring neurons with allatostatin or HM4D Gi/o-coupled receptors, we analyzed

52 2012) showed that bath application of C-type allatostatin produced either increases or decreases in t

53 in vitro using expression of the Drosophila allatostatin receptor (AlstR).

54 ity; Channelrhodopsin-2 for photoactivation; allatostatin receptor for inactivation by ligand applica

55 ociated virus 2, we expressed the Drosophila allatostatin receptor in somatostatin (Sst)-expressing n

56 aterally to express an inhibitory Drosophila allatostatin receptor were silenced by application of an

57 G-protein-coupled receptor AlstR (Drosophila allatostatin receptor) [corrected] after application of

58 acutely by ligand-induced activation of the allatostatin receptor.

59 rgic C1 neurons, using inhibitory Drosophila allatostatin receptors, for the enhanced expiratory-rela

60 e peptides, tyrosine hydroxylase, proctolin, allatostatin, serotonin, Cancer borealis tachykinin-rela

61 g the viral CREB-expressing neurons with the allatostatin system occludes the spatial memory enhancem

62 Proctolin, serotonin, and allatostatin were also physiologically active on the iso

63 An antiserum to cockroach allatostatins (YXFGLamides) was shown to recognize lepid