ライフサイエンスコーパス: depressor

1 rates for the future investigation of aortic depressor afferent physiology, structural remodeling of

2 the pressor agent phenylephrine (PE) and the depressor agent sodium nitroprusside (SNP) in 57 urethan

3 When baroreceptor innervation (aortic depressor amd carotid sinus nerves) was intact, rhythms

4 t of VAGSTIM was specific for ERSNA, because depressor and bradycardia responses to VAGSTIM were unaf

5 tachycardic response which was followed by a depressor and bradycardic response; when high concentrat

6 l cerebrospinal (aCSF) fluid, confirmed that depressor and bradycardic responses are elicited from al

7 e medial subnucleus of the NTS (mNTS) elicit depressor and bradycardic responses via activation of io

8 The maximum depressor and bradycardic responses were elicited by a 1

9 njections of l-Glu remained unchanged, i.e., depressor and bradycardic responses were elicited from a

10 tory effects of E-2 in the mNTS resulting in depressor and bradycardic responses, on one hand, and in

11 Baroreceptor stimulation elicited depressor and bradycardic responses.

12 ceptin (0.15-0.62 mM) into the nCom elicited depressor and bradycardic responses.

13 e nucleus tractus solitarius (nTS) to elicit depressor and bradycardic responses.

14 (CS), have been generally reported to elicit depressor and bradycardic responses.

15 (2) activation of these receptors results in depressor and bradycardic responses; (3) for a complete

16 In sham rats, BDNF evoked a dose-dependent depressor and sympatho-inhibitory effect and ANA-12 prod

17 Each set consists of one pair of erector, depressor, and inclinator muscles.

18 litation (SICF)) in two typical muscles, the depressor anguli oris (DAO), a face muscle, and the firs

19 EMG activity recorded from the frontalis and depressor anguli oris during a contrived expression.

20 during the horror look and the frontalis and depressor anguli oris during one of the contrived expres

21 cus major during smiling, the corrugator and depressor anguli oris during the sad look and the fronta

22 robably more prevalent in the corrugator and depressor anguli oris during the sad look, the frontalis

23 ar excitability and neural plasticity in the depressor anguli oris M1.

24 paired associative stimulation (PAS) in the depressor anguli oris muscle (DAO).

25 ercilii, levator labii, frontalis lateralis, depressor anguli oris, zygomaticus major) whilst partici

26 inhibitory intracortical circuits in a face (depressor anguli oris; DAO) and hand (first dorsal inter

27 ocated in the caudal ventrolateral medullary depressor area (CVLM) in regulating/modulating cardiovas

28 ea (RVLM) and caudal ventrolateral medullary depressor area (CVLM), and the nucleus tractus solitariu

29 were found ipsilaterally in the pressor and depressor areas of the medulla and the spinal trigeminal

30 The male anal depressor begins to change in the L3 stage, first by ret

31 DHK produced depressor, bradycardic and sympathoinhibitory responses

32 Wooden tongue depressors can be a vehicle for transmission of mucormyc

33 MS and control site responses to pressor and depressor challenges during sleep that resulted in somat

34 es differed in direction between pressor and depressor challenges, neural activity increased later in

35 tivity declines and increases to pressor and depressor challenges, respectively.

36 phic color pattern in that levator (Lev) and depressor (Dep) of females tend to be much darker than t

37 We studied the Caenorhabditis elegans anal depressor development in larval males and hermaphrodites

38 timulation of the MPO produces a distinctive depressor effect that is mediated through the PAG.

39 ating that AT2 receptor does not exert acute depressor effects in these mice lacking AT1 receptors.

40 al because the receptor has both pressor and depressor effects in vivo.

41 , was assessed as being a potent respiratory depressor in rodents.

42 tly reduced in guard cells of K+(in) channel depressor lines.

43 rom leaves was reduced in the K+(in) channel depressor lines.

44 n that the M. protractor pterygoideus and M. depressor mandibulae act on the quadrate as a pure torqu

45 Pressor and depressor manipulations are usually followed by compensa

46 The use of a new depressor marker facilitated a quick and effective flow

47 The newly developed scleral depressor marker facilitated simultaneous indentation an

48 ntified leg motoneurons (such as the femoral depressor motoneuron) expressed detectable levels of TM-

49 th silence of the slow and fast trochanteral depressor motoneurons and activation of the common inhib

50 Bursts of trochanteral levator and depressor motoneurons were clearly coordinated between t

51 (fSR) makes direct cholinergic synapses with depressor motor neurons (MN) controlling that wing, incl

52 MGs and with differences in the responses of depressor motor neurons recorded in reduced, in vitro pr

53 the same status-dependent differences as the depressor motor neurons.

54 levation/depression and trochanteral levator/depressor muscle bursts, suggesting that the neural modu

55 h simultaneously recorded differences in leg depressor muscle EMGs and with differences in the respon

56 In both sexes, the larval anal depressor muscle is used for defecation behavior.

57 lossal (GG) muscle is the main protruder and depressor muscle of the tongue and contributes to upper

58 A smaller depressor muscle, M133a, is innervated by two neurons, o

59 The large trochanteral depressor muscle, M133b,c, is innervated by two motor ne

60 dites and larval males, the single cell anal depressor muscle, used for waste expulsion, contains bil

61 y killing the SPC motor neurons and the anal depressor muscle: cells that directly contact the protra

62 n activation of the dorsal longitudinal wing-depressor muscles (DLMs).

63 ameter values are based on measurements from depressor muscles and observations of kinematics and dyn

64 s generated by slow contractions of hind leg depressor muscles and then stored by bending specialised

65 adhesive bandages (19 cases), wooden tongue depressors (n = 5), ostomy bags (n = 2), water circuitry

66 ited by electrical stimulation of the aortic depressor nerve (ADN) at 5 Hz or 15 Hz in urethane anest

67 eptor neurones identified by attached aortic depressor nerve (ADN) boutons.

68 of the solitary tract (NTS) receiving aortic depressor nerve (ADN) inputs was examined during blood p

69 ns of 20 s were delivered to the left aortic depressor nerve (ADN) of these rats using low ranges of

70 ified according to their responses to aortic depressor nerve (ADN) stimulation: monosynaptic neurones

71 iodide transported from the cervical aortic depressor nerve (ADN) to stain central terminals.

72 Aortic depressor nerve activity (ADNA) was measured while AP wa

73 y for chemoreceptor afferents or onto aortic depressor nerve for baroreceptor afferents.

74 activities from aortic baroreceptors in the depressor nerve in anesthetized rabbits and examined the

75 ormed during control, after bilateral aortic depressor nerve section, after bilateral cervical vagus

76 vagus nerve section, after bilateral aortic depressor nerve section, and during central aortic depre

77 In protocol B, central aortic depressor nerve stimulation decreased ERSNA and peak hei

78 sor nerve section, and during central aortic depressor nerve stimulation.

79 isible response to stimulation of the aortic depressor nerve.

80 projections of the carotid sinus and aortic depressor nerves.

81 ast three adult-specific muscles, the tergal depressor of the trochanter and dorsoventral muscles I a

82 n the number of fibers comprising the tergal depressor of the trochanter muscle (TDT, or jump muscle)

83 as TpnC41C is the main isoform in the tergal depressor of the trochanter muscle (TDT; jump muscle).

84 entobarbitone-anaesthetized animals, the jaw-depressor reflex (JDR) evoked by stimulation of the tong

85 rent nerves can evoke a Bezold-Jarisch (B-J) depressor reflex in anaesthetized rats.

86 potension due to the activation of a second 'depressor' reflex.

87 medulla (CVLM) to a physiologically defined depressor region.

88 ion (VRS) in an anaesthetized mouse causes a depressor response and a reduction in HR.

89 Lidocaine pretreatment also inhibited the depressor response caused by intramuscular formalin (5%;

90 lateral hypothalamus (LH) contributes to the depressor response evoked by somato-visceral nociception

91 t the hypothesis that the vlPAG mediates the depressor response evoked by visceral nociception and in

92 into anesthetized rats elicited a transient depressor response followed by pronounced pressor respon

93 profile and their predominant cardiovascular depressor response to anandamide is mediated through CB(

94 PVNx also lowered the depressor response to ganglionic blockade (AL-PVNx=-28+/

95 BP (AL=152+/-5; FR=113+/-2 mmHg), less of a depressor response to ganglionic blockade (AL=-58+/-4; F

96 The depressor response to Isop was significantly attenuated

97 MSA patients had a marked depressor response to low infusion rates of trimethaphan

98 epressor response to trimethaphan also had a depressor response to phentolamine.

99 Patients having a depressor response to trimethaphan also had a depressor

100 consisting of the Bezold-Jarisch-associated depressor response, a pressor action, and long-lasting d

101 4 had no effect on the endothelin-B-mediated depressor response, whereas SB-209,670 abolished it.

102 response, a pressor action, and long-lasting depressor response.

103 IGRL (1 mg/kg, bolus) produced only a marked depressor response.

104 tissue surrounding these receptors elicits a depressor response.

105 s from the lateral column vs. quiescence and depressor responses from the ventrolateral column), rais

106 sion in RA+ mice, we determined the relative depressor responses to intravenous administration of the

107 VLM were functionally defined by pressor and depressor responses to microinjected GABA (500 pmol, 50

108 adycardia, reduction in lumbar SNA, and both depressor responses were equivalent in sham-lesioned and

109 /kg) without cocaine produced dose-dependent depressor responses with recovery typically within 2 hrs

110 eceptors to prevent sympathetically mediated depressor responses, OZRs still had reduced sympathetic

111 ysteic acid (DLH) elicited either pressor or depressor responses.

112 giotensin II, and hypoxia; enhance pulmonary depressor responses; and attenuate pulmonary hypertensio

113 his demarcation is not dependent on the anal depressor's intrinsic genetic sex, but is influenced by

114 lpha and IR beta), and that both pressor and depressor sites are present in both areas.

115 emical stimulation at identified pressor and depressor sites in the lateral and ventrolateral periaqu

116 At PVN depressor sites twelve RVL neurones were inhibited prior

117 ump movement itself, which occurred when the depressor spikes ceased and which lasted 1 ms.

118 ps in the dimorphic re-sculpting of the anal depressor that are regulated by genetic sex and by cell-

119 of pressor surges and greater prominence of depressor valleys during long-term follow-up.

120 eas unc-94b is expressed in pharyngeal, anal depressor, vulval and uterine muscles and in spermatheca

121 o address when the changes occur in the anal depressor, we used YFP:actin to monitor, and mutant anal

122 of infection was identified as wooden tongue depressors, which were used on the nursery to construct

123 For this purpose, a wooden tongue depressor (WTD) is laser-treated and converted to an ele