ライフサイエンスコーパス: chloral

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1 turation with pentobarbital (0.2%) than with chloral hydrate (1.6%) (P <.01).

2 0-294]) > 2,2,2-trichloro-(215% [196-234]) > chloral hydrate (165% [161-176]) > 2,2-dichloro- > 2-chl

3 as lower with pentobarbital (0.5%) than with chloral hydrate (2.7%) (P <.001).

4 (3.0-7.0 mg per kilogram of body weight) or chloral hydrate (50-75 mg/kg).

5 s achieved with pentobarbital (3-5 mg/kg) or chloral hydrate (75 mg/kg).

6 Mean doses were 50 mg/kg chloral hydrate and 4 mg/kg pentobarbital.

7 cumulation were inhibited by ALDH inhibitors chloral hydrate and daidzin.

8 Chloral hydrate and dichloroacetic acid were not detecte

9 Valproic acid, chloral hydrate and newer-generation antiepileptics are

10 micrograms estradiol, were anesthetized with chloral hydrate and stereotaxically implanted with dialy

11 nt study controlled these variables by using chloral hydrate anesthesia, testing 'depressed' rats at

12 in awake, unrestrained conditions and during chloral hydrate anesthesia.

13 wo conditions: awake, unrestrained and under chloral hydrate anesthesia.

14 Using chloral hydrate anesthetized rats, dopamine (DA) agonist

15 Although oral pentobarbital and oral chloral hydrate are equally effective, the incidence of

16 26.4 weeks, were studied after sedation with chloral hydrate at between 11 and 14 months of age, corr

17 hese results, together with the finding that chloral hydrate completely blocked the D1 inhibition, ma

18 ants who received oral pentobarbital or oral chloral hydrate for sedation between 1997 and 2002 were

19 ecreased reactivities for trihalomethane and chloral hydrate formation and divergent reactivities for

20 There was no change in reactivity for chloral hydrate formation, while WEOM from black ash sho

21 uced or abolished when cilia were removed by chloral hydrate or when ciliary-associated proteins poly

22 e stained with aniline blue and cleared with chloral hydrate to allow high-resolution confocal imagin

23 al analysis of primary cilia; or exposure to chloral hydrate to damage or remove primary cilia and 2

24 CD-1 mice anesthetized by chloral hydrate were subjected to global ischemia by bil

25 hloralose, 2,2,2-trichloroethanol [TCE], and chloral hydrate), to ethanol, and to a panel of halogena

26 tions of trihalomethanes, haloacetonitriles, chloral hydrate, and haloketones.

27 Agents such as chloral hydrate, barbiturates, and benzodiazepines that

28 azepam, clonazepam, propofol, pentobarbital, chloral hydrate, halothane, isoflurane, sevoflurane, enf

29 ate anesthesia produced by administration of chloral hydrate, ketamine, or halothane significantly re

30 BA(A))-enhancing class (e.g., pentobarbital, chloral hydrate, muscimol, and ethanol) produce analgesi

31 sedation regimens--which included fentanyl, chloral hydrate, pentobarbital, and midazolam hydrochlor

32 sthesia showed that pentobarbital, ketamine, chloral hydrate, urethane, or metofane eliminated evoked

33 to six weeks later, the L4-L6 spinal cord of chloral hydrate-anesthetized animals was exposed, and ce

34 ocular pressure for 30, 45, or 60 minutes in chloral hydrate-anesthetized ND4 Swiss-Webster mice.

35 spontaneous discharge rate of LC neurons in chloral hydrate-anesthetized rats and the role of CRF re

36 ter the activities of SNpr neurons in either chloral hydrate-anesthetized rats or awake locally anest

37 In chloral hydrate-anesthetized rats, extracellular single-

38 rease spiking rate of VP neurons recorded in chloral hydrate-anesthetized rats.

39 s concurrently with reverse microdialysis in chloral hydrate-anesthetized rats.

40 phoretic application of treatment ligands in chloral hydrate-anesthetized rats.

41 ytochrome P-450 monooxygenase, which produce chloral hydrate.

42 50 mg/kg chloral hydrate; 5-10 kg, 100 mg/kg chloral hydrate; 10-20 kg, 1 mg/kg temazepam plus 0.25 m

43 age from conception: weight <5 kg, 50 mg/kg chloral hydrate; 5-10 kg, 100 mg/kg chloral hydrate; 10-

44 NAD and chloral when used together protected against inactivatio

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