ライフサイエンスコーパス: pentobarbitone

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1 ivity and asystole (by high-dose intravenous pentobarbitone).

2 , of GABA potentiation by either propofol or pentobarbitone.

3 laevis oocytes were augmented by propofol or pentobarbitone.

4 fractory to activation by either propofol or pentobarbitone.

5 ension and apnoea in rats anaesthetized with pentobarbitone.

6 and were potentiated by chlordiazepoxide and pentobarbitone.

7 a-pigs (150-300 g) anaesthetized with sodium pentobarbitone.

8 t (meditomidine hydrochloride 0.5 mg kg(-1), pentobarbitone 10 mg kg(-1) i.v.), 125I-T4 was perfused

9 fect the baroreceptor reflex (P > 0.2) while pentobarbitone (100 microM) significantly and reversibly

10 Pentobarbitone (50-100 microM) was effective in enhancin

11 y the LH pulse-suppressing anesthetic sodium pentobarbitone, a small rise in core temperature occurs

12 In intact, pentobarbitone-anaesthetized animals, the jaw-depressor

13 performed in lumbar motoneurones of intact, pentobarbitone-anaesthetized cats.

14 gs with microiontophoresis were performed in pentobarbitone-anaesthetized, paralysed and artificially

15 In cats anaesthetized with sodium pentobarbitone and breathing spontaneously following tra

16 by beta 3 subunit homomers, was enhanced by pentobarbitone and inhibited by picrotoxinin.

17 the rats were anaesthetized with urethane or pentobarbitone and prepared for blood sampling to determ

18 In rabbits anaesthetised with pentobarbitone and prepared with minimal surgical interf

19 For murine beta 1 subunits, both pentobarbitone and propofol increased the membrane condu

20 at the heel or at the toes in pre-immunized, pentobarbitone-anesthetized rabbits.

21 s tested showed no sensitivity to etomidate, pentobarbitone or diazepam.

22 e direct activation of the GABAA receptor by pentobarbitone (PB) and phenobarbitone (PHB) was charact

23 In decerebrated, spinalised, pentobarbitone-sedated animals, mustard oil applied to a

24 In non-spinalised, decerebrated, pentobarbitone-sedated preparations, flexor reflexes wer

25 %, 6:7), etomidate (43.9 +/- 36 %, 6:8) and pentobarbitone sodium (41 %, 1:1), and were depressed by

26 Experiments were performed on anaesthetised (pentobarbitone sodium 60 mg kg-1 I.P., then 10 mg kg-1 I

27 in the dorsal vagal motor nucleus (DVMN) of pentobarbitone sodium anaesthetized rats.

28 afferent nerves supplying the jejunum in the pentobarbitone sodium-anaesthetised rat.

29 ol were similarly affected, whereas those of pentobarbitone were unaltered.

30 289Mgamma2L) were potentiated by propofol or pentobarbitone with approximately 2-fold reduced potency

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