ライフサイエンスコーパス: morphine sulfate

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1 th acute administration of 10 or 30 mg/kg of morphine sulfate.

2 s rats were given one intra-VTA injection of morphine sulfate (0.0, 0.01, or 0.03 microg, in saline)

3 ; 43 received premedication with intravenous morphine sulfate (0.04 mg per kilogram of body weight) a

4 ntrolled study using 4 weeks of slow-release morphine sulfate and a corresponding period of matched p

5 eceiving continuous intravenous infusions of morphine sulfate and requiring ECMO.

6 Morphine sulfate causes immunomodulatory and immunosuppr

7 intravenous narcotic use (9.2 vs 17.2 mg of morphine sulfate equivalents, P = .03) were significantl

8 rats received 0, 0.6, 1.25, 2.5, or 5 mg/kg morphine sulfate (i.p.) for 4 days, and vehicle only for

9 in areas, 7 additional males received 20 mug morphine sulfate ICV following ethanol injection (ME).

10 We tested the hypothesis that morphine sulfate in the dose of 5 mg twice daily would b

11 ed from noninfected animals and treated with morphine sulfate in vitro produced an increase in the ex

12 Morphine sulfate is an effective antitussive in intracta

13 thing or a unilateral intra-VTA injection of morphine sulfate (MS) (0.0, 0.01, 0.03, 0.1 or 0.3 micro

14 oliferation, 20 nmol/2 microliters of either morphine sulfate or DAMGO (mu-selective agonist) were ad

15 cted twice daily for a total of 20 days with morphine sulfate or saline beginning at 30 days of age.

16 res was noted among patients on slow-release morphine sulfate (p < 0.01).

17 es including small molecules (norepinephrine-morphine sulfate), protein-protein complexes (insulin-gl

18 mal saline injection, (3) rats injected with MORPHINE sulfate subcutaneously, and (4) rats treated wi

19 Addition of morphine sulfate to human CEMx174 lymphocytic cells resu

20 he lateral ventricles and 0, 2, 5 micrograms morphine sulfate was administered intracerebroventricula

21 Then, 0.04 mg/kg intravenous morphine sulfate was administered, followed by imaging f

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