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The Analgesic Activity of Morphine-6-glucuronide

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Specialty Pharmacology
Date 1992 Aug 1
PMID 1419474
Citations 49
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Abstract

1. The pharmacokinetics, cardio-respiratory effects and analgesic effects of intravenous morphine-6-glucuronide were studied in 20 cancer patients with pain. Four different dose levels (0.5, 1, 2, and 4 mg 70 kg-1) were studied. Plasma concentrations of morphine-6-glucuronide were measured for 12 h after dosing. Pulse rate, respiratory rate and blood pressure were monitored, and pain relief was measured using two rating scales and a visual analogue scale. 2. The mean elimination half-life (+/- s.d.) of morphine-6-glucuronide was 3.2 +/- 1.6 h. The mean AUC standardised to a dose of 1 mg 70 kg-1 was 390 +/- 263 nmol l-1 h. Mean morphine-6-glucuronide clearance was 96 +/- 38 ml min-1. There was a direct relationship between morphine-6-glucuronide plasma clearance and calculated creatinine clearance (r = 0.81, P less than 0.001). 38 +/- 22% of the dose of morphine-6-glucuronide was recovered unchanged in the urine in 24 h. No morphine or morphine-3-glucuronide was detected in the plasma or urine of any patient after morphine-6-glucuronide treatment. 3. Morphine-6-glucuronide exerted a useful analgesic effect in 17/19 assessable patients for periods ranging between 2 and 24 h. No correlation was observed between dose or plasma morphine-6-glucuronide concentrations, and duration or degree of analgesia. No clinically significant changes in cardio-respiratory parameters were observed. No patients reported sedation or euphoria. Nausea and vomiting were notably absent in all cases. 4. Morphine-6-glucuronide is an effective and well-tolerated analgesic. It is likely that the majority of the therapeutic benefit of morphine is mediated by morphine-6-glucuronide.(ABSTRACT TRUNCATED AT 250 WORDS)

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References
1.
Rigg J . Ventilatory effects and plasma concentration of morphine in man. Br J Anaesth. 1978; 50(8):759-65. DOI: 10.1093/bja/50.8.759. View

2.
Woods L . Distribution and fate of morphine in non-tolerant and tolerant dogs and rats. J Pharmacol Exp Ther. 1954; 112(2):158-75. View

3.
Osborne R, Joel S, TREW D, Slevin M . Morphine and metabolite behavior after different routes of morphine administration: demonstration of the importance of the active metabolite morphine-6-glucuronide. Clin Pharmacol Ther. 1990; 47(1):12-9. DOI: 10.1038/clpt.1990.2. View

4.
Pasternak G, Bodnar R, Clark J, Inturrisi C . Morphine-6-glucuronide, a potent mu agonist. Life Sci. 1987; 41(26):2845-9. DOI: 10.1016/0024-3205(87)90431-0. View

5.
Pasternak G, Wood P . Multiple mu opiate receptors. Life Sci. 1986; 38(21):1889-98. DOI: 10.1016/0024-3205(86)90217-1. View