ライフサイエンスコーパス: vasotocin

1 avian receptor homologous to the V1aR is the vasotocin 4 receptor (VT4R).

2 ors with two radioligands, [(125)I]ornithine vasotocin analog ([(125)I]OVTA) and [(125)I]linear VP an

3 duction pathways underlying acute effects of vasotocin and corticosterone, presumably mediated via "n

4 ians, the hypothalamic neuropeptide arginine vasotocin and the adrenal steroid corticosterone interac

5 es with synthetic oligonucleotide probes for vasotocin and the related neuropeptide mesotocin, as wel

6 with an emerging pattern of distribution of vasotocin- and vasopressin-like peptides in vertebrates.

7 ations are compared with previous studies of vasotocin- and vasopressin-like systems in vertebrates.

8 ecause most classes, except for mammals, use vasotocin as the natural ligand for that receptor.

9 T; hereafter OT) and arginine vasopressin or vasotocin (AVP or VT; hereafter VT) are neurotransmitter

10 The arginine vasopressin/vasotocin (AVP/AVT) system is strongly androgen dependen

11 ra and interspecific comparisons of arginine vasotocin (AVT) and its mammalian homolog arginine vasop

12 Arginine vasotocin (AVT) and its mammalian homologue arginine vas

13 he neuroanatomical distributions of arginine vasotocin (AVT) and mesotocin (MST), non-mammalian homol

14 In fishes, arginine vasotocin (AVT) expression is related to social and/or r

15 trometry, we identified the peptide arginine vasotocin (AVT) in brain and pituitary extracts from the

16 demonstrated that isotocin (IT) and arginine vasotocin (AVT) modulate fictive vocalizations divergent

17 Arginine8 vasotocin (AVT), a neurohypophyseal peptide in nonmammal

18 mals (i.e., distributions of met-enkephalin, vasotocin, galanin, calcitonin gene-related peptide, tyr

19 CT-H), which emphasizes the role of oxytocin-vasotocin hormones, touch, and enduring bonds in the evo

20 in situ hybridization, we conclude that the vasotocin immunohistochemical procedures used identify v

21 typical group sizes, we now demonstrate that vasotocin-immunoreactive (VT-ir) neurons of the BSTm exh

22 he highest sensitivity is attained with arg8-vasotocin, in which a total of 300 amol is detected in a

23 Arg8-vasotocin isolated from the pineal gland of rainbow trou

24 ural vocalizations was modulated by arginine-vasotocin, isotocin and their antagonists delivered to t

25 nt of whole brain minces with vasopressin or vasotocin led to increases in PKCalpha in membrane fract

26 The distribution of arginine vasotocin-like systems in T. granulosa is greater than t

27 the neuroanatomical distribution of arginine vasotocin-like systems in the roughskin newt (Taricha gr

28 immunohistochemical procedures used identify vasotocin-like, but not mesotocin-like, elements in the

29 Several additional vasotocin-like-immunoreactive cell groups were observed

30 Arginine vasotocin-like-immunoreactive fibers and presumed termin

31 Vasotocin-like-immunoreactive neuronal cell bodies were

32 es were immunofluorescently multilabeled for vasotocin, mesotocin (MT), corticotropin-releasing hormo

33 als) and its evolutionary precursor arginine-vasotocin (non-mammals) modulate reproductive physiology

34 xpress galanin and the nonapeptides arginine-vasotocin or isotocin, homologues of mammalian arginine

35 eceptor antagonist ([d(CH2)5-Tyr (Me)2-Orn8]-Vasotocin [OTA]; 25 microg i.t. in 5 microl saline) sign

36 ntagonist [d(CH(2))(5), Tyr (Me)(2), Orn(8)]-vasotocin (OVT).

37 xamine the effects of corticosterone and the vasotocin receptor agonist arginine vasopressin, alone a

38 We identified six major oxytocin-vasotocin receptors among vertebrates.

39 ithin the brain, while calcitonin, SIFamide, vasotocin, RGWamide, DLamide, FLamide, FVamide, MIP, and

40 es that acoustically court females (arginine-vasotocin-sensitive) than in females and sneak-spawning

41 urodele amphibians possess a well-developed vasotocin system, perhaps more extensive than other vert

42 Vasopressin or vasotocin treatment also induced the appearance in membr

43 V1 vasopressin receptor agonist, [Phe2,Orn8]-vasotocin, (V1 agonist) induced a significant accumulati

44 rmones, including pigment-dispersing factor, vasotocin (vasopressin/oxytocin) and neuropeptide Y.

45 iated through interactions with the arginine vasotocin/vasopressin (AVT/AVP) system.

46 Aromatase, the neuropeptides arginine vasotocin/vasopressin, and the monoamine neurotransmitte

47 Vasotocin (VT) and its mammalian homologue, vasopressin

48 Isotocin (IT) and vasotocin (VT) are the teleost homologues of these genes

49 Vasotocin (VT) inhibited approach responses toward the v

50 leotide phosphotase diaphorase, and arginine vasotocin were used in the present study.