ライフサイエンスコーパス: guanethidine

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1 ine and the adrenergic neuron-blocking agent guanethidine.

2 reatment with the adrenergic neuron blocker, guanethidine (20 mg/kg), also abolished the PVN-mediated

3 sions of the mesentery and by application of guanethidine (3 microM) to the stimulation and recording

4 In contrast, neither splanchnectomy nor guanethidine (5 mg kg(-1)) had an effect.

5 Pretreatment with subcutaneous guanethidine (5 mg/kg) and propranolol (1 mg/kg), but no

6 oxamine (6-20 microM) and in the presence of guanethidine (5 microM), EFS of perivascular sensorimoto

7 rivative, displays the same pH dependence as guanethidine, a heptamethyleniminoethyl- guanidine deriv

8 These events are stimulated by NE and by guanethidine, an hNET substrate, and they are blocked by

9 ing NET is metaiodobenzylguanidine (MIBG), a guanethidine analog of norepinephrine.

10 HDA] treatment) and long-term sympathectomy (guanethidine and 8 days after 6-OHDA) on the distributio

11 In the presence of atropine, guanethidine and propranolol, electrical field stimulati

12 88.6+/-10.9% (n=5) and 80.4+/-2.2% (n=5) by guanethidine and propranolol, respectively.

13 TX, C6 and L-NAME, but not by VIP antiserum, guanethidine and splanchnicotomy.

14 s blocked by tetrodotoxin, nitro-L-arginine, guanethidine, and beta2-adrenoceptor antagonists.

15 were antagonized by postganglionic action of guanethidine, but not by phentolamine or suramin.

16 Guanethidine completely suppressed the heat hyperalgesia

17 he release of sympathetic neurotransmitters (guanethidine or reserpine) inhibited capsaicin-evoked iC

18 with atropine or hexamethonium but not with guanethidine or vagotomy.

19 tive intestinal polypeptide (VIP) antiserum, guanethidine, or splanchnicotomy.

20 Guanethidine pretreatment attenuated myenteric but not D

21 of sympathetic fiber function with systemic guanethidine significantly decreased the pain-related be

22 ale Sprague-Dawley rats were pretreated with guanethidine sulfate (40 mg/kg daily for 5 weeks) or veh

23 cted 50% with noradrenaline and treated with guanethidine (to inhibit sympathetic neurotransmission),

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