Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0344307 (analgesia)
 28,200 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Effects of dietary proteins such as casein and egg albumin on analgesic activity of, tolerance to and physical dependence on morphine in rats were examined. There was no difference in analgesic activity after acute administration of morphine 10 mg/kg, s.c. between rats treated with casein food or egg albumin food and normal food for 5 or 21 days. The development of tolerance to morphine analgesia in rats treated with albumin food but not with casein food was suppressed during daily morphine 10 mg/kg, s.c. on 5 consecutive days. Rats were treated with casein or albumin food mixed with morphine (0.5 mg/g of food) for 5 days. Morphine intake in rats treated with albumin food was significantly decreased as compared to that with morphine admixed casein or normal food. Body weight loss by naloxone in morphine-dependent rats was significantly less in both casein food and albumin food groups than in the normal food group. These results suggest that chronic dietary treatment with albumin may produce a partial inhibition of development of tolerance to morphine analgesia and that with casein may attenuate morphine withdrawal manifestation in rats.
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PMID:[Effects of dietary proteins on analgesic activity of tolerance and physical dependence on morphine in rats]. 135 65

Pregnant rats were given diets containing either 5% ethanol, an isocaloric (pair-fed) diet, or casein pellets. Offspring were tested at postnatal day 10 for isolation-induced ultrasonic vocalizations and subsequent stress-induced analgesia. Rats prenatally exposed to ethanol vocalized significantly less in the five minutes during isolation. The opiate, morphine, caused a greater suppression of vocalizations in alcohol-exposed pups compared to controls, while the increased calling normally seen with the opiate antagonist, naltrexone, was attenuated. In a test in which the pup withdraws a paw from a hot plate (48 degrees C), prenatal alcohol offspring demonstrated baseline latencies (no isolation) similar to controls but had greatly attenuated responses in their isolation-induced analgesia. Since both vocalization and analgesia responses have been determined to be modulated by the endogenous opioid system, the aberrant responses of the prenatal-ethanol-exposed offspring can be interpreted as failures to respond by opioid release/secretion to appropriate stimuli.
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PMID:Opioid-dependent behaviors in infant rats: effects of prenatal exposure to ethanol. 194 79

The effects of undernutrition on novelty-induced analgesia were investigated in young and adult rats. Rats were undernourished by feeding their dams an 8% casein diet from birth until weaning (21 days of age). Rats were exposed to an open field (novelty) for 2 min and the nociception was measured by the tail-flick method. At adult age, only well-nourished rats presented novelty-induced analgesia, suggesting that early undernutrition abolishes this response. At 21 days of age, the exposure to the open field had no effect on nociception of both nutritional groups, suggesting that some developmental factor is necessary for the emergence of novelty-induced analgesia.
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PMID:Effects of undernutrition during suckling on novelty-induced analgesia in young and adult rats. 215 67

Stress-induced analgesia was evaluated in adult rats submitted early in life to a protein deprivation schedule. Rats were undernourished with a hypoproteic diet containing 80 g casein/kg diet from d 14 of gestation until 50 days of age. Rats were thereafter fed a balanced nonpurified diet until 140 days of age, when they were exposed to two stressors: forced swimming and acute restraint, after which the analgesic response was evaluated. In addition, the analgesic response induced by different morphine doses was determined in another group of rats. Basal latency was not different in deprived and control rats. Undernourished rats presented a significantly lower analgesic response in both stress situations. However, when the analgesic response induced by different morphine doses (1, 2, 4 and 8 mg/kg, s.c.) was assessed, a significantly higher response occurred in undernourished rats compared to control rats. This lower stress-induced analgesia in undernourished rats may account for the behavioral alterations attributed to early undernutrition.
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PMID:Analgesic response to stress is reduced in perinatally undernourished rats. 916 99

Weaning rat pups at day 21 activates a delta-opioid receptor that mediates swim-stress-induced analgesia (swim SIA). We have addressed the possibility that removal of maternal milk is the stimulus for the weaning-induced delta-receptor activation by studying the effect of lactating and nonlactating surrogate mothers and two milk substitutes (casein-rich and casein-free) on opioid receptor control of swim SIA. The delta-receptor antagonist naltrindole (1 mg/kg) significantly antagonized swim SIA in 25-day-old weaned rats, in rats provided with a nonlactating surrogate, and those provided with casein-free milk substitute. Naltrindole had no effect in nonweaned pups, pups given a casein-rich substitute, or in pups from litters provided with a lactating surrogate from day 21 to day 25. Weaning-induced activation of delta-receptors involved in mediating swim SIA appears to be dependent on the loss of dietary casein, which is known to produce peptide fragments that can exert opioid activity. The data suggest that exposure to exogenous opioid peptides can influence the ontogenesis of mu- and delta-opioid receptors.
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PMID:Influence of maternal milk on functional activation of delta-opioid receptors in postnatal rats. 1118 1

The present work sought to study the binding properties of central mu-opiate receptors in whole brain and in different central areas in adult rats undernourished at perinatal age. Rats were undernourished with a hypoproteic diet containing 8% casein from day 14 of gestation until 50 days of age. The animals were thereafter fed a balanced commercial chow until 140 days of age. At this time point the experiments started. 3H-D-Ala2, N-Me-Phe4, Gly5-ol-enkephalin (3H-DAMGO) was used to selectively label the mu-receptors. The results obtained demonstrated that perinatal undernutrition induced, in the adult animal, a decreased mu-receptors density (Bmax) both in whole brain as well as in midbrain, without significant changes in affinity. In addition, no changes were found in mu-specific binding in the cortex of these undernourished animals. Taking into account that recent evidences from our laboratory have demonstrated a lower stress-induced analgesia following exposure to different stressful situations in rats undernourished in early life, the present findings seem to suggest that this lower analgesic response could be due, at least in part, to a lower density of mu-opiate receptors in the brain.
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PMID:Perinatal undernutrition: changes in brain opiate receptor density. 1192 98