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Query: UNIPROT:Q86TM3 (cage)
 29,987 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The effects of handling, ether vapor anesthesia and blood sampling on serum LH and prolactin were determined in intact, castrate and dexamethasone-treated male rats. Cage removal and transport to an adjacent room increased LH and prolactin levels by 10 and 15 min after the initial animal disturbance. Intact male rats subjected to repeated ether anesthesia and blood sampling showed a more rapid increase in serum LH and prolactin than the preceding rats, since serum LH and prolactin was increased by 4, 8 and 15 min after initial cage disturbance. In a group of rats subjected to serial blood sampling over a longer time interval, both prolactin and LH levels remained higher than 90 min after initial animal handling. At 90 minutes after a single blood sampling, blood prolactin concentration remained higher than in controls. Serum LH levels returned to control levels 90 min after the stress of a single blood sampling. Although serum prolactin was increased in the castrate group subjected to serial anesthesia and blood sampling, LH concentrations were reduced under the same conditions. Injection of 5 and 50 mug of dexamethasone/100 g body wt for 8 days markedly reduced adrenocortical responsiveness to the stress of serial anesthesia and blood sampling at 1, 4, 8 and 15 min after initial rat disturbance. The 50 mug dexamethasone treatment reduced the stress-stimulated increase in serum prolactin at all blood sampling intervals. The dexamethasone-treated groups also showed smaller increases in serum LH at 8 and 15 min after first animal handling than the control rats. These results indicate that serum LH and prolactin concentrations are consistently increased by acute stress in intact male rats, the duration of the stress stimulation of LH and prolactin is at least 90 min under the conditions of this study, serum LH levels of castrate male rats are decreased by acute stress and dexamethasone administration lowers stress stimulation of LH and prolactin release.
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PMID:Effects of acute stress on serum LH and prolactin in intact, castrate and dexamethasone-treated male rats. 110 6

The literature reveals contradictory data regarding whether or not male release LH acutely following coitus. Since it has been shown that repeated mating increases accessory sex organ weight, suggesting induction of gonadotrophin release, it seemed of interest to reinvestigate the issue. Male rats were divided into two groups: the mated group was provided with frequent mating ("experiencing") trials; the unmated group served as cage controls which received no sexual contact throughout the entire experiment. All rats were provided with chronic jugular cannulae. One set of serum samples was taken from each rat at 85 days, the second set at 115 days. On the two evening when sampling took place the mated rats were subdivided into three groups: "chamber" (placed in mating arena alone), "mount" (allowed two to five mounts, but no intromission), and "ejaculation" (mated through entire copulatory sequence). Serum sampling took place every 15 min during the hour following completion of mating (defined in the "ejaculation" group). On the day following the second sampling, autopsies were performed, and terminal serum samples were taken. LH, FSH, and prolactin were measured by radioimmunoassay. There were no significant differences in any hormone among the groups during the hour following mating nor in the terminal sample. However, the mated rats showed significantly greater seminal vesicle and ventral prostate weights than the cage controls at autopsy. Several hypotheses are offered to account for the latter findings.
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PMID:Effects of mating on serum LH, FSH, and prolactin and accessory tissue weight in male rats. 124 58

In an effort to determine the inductive component(s) of photic input in long day seasonal breeders, adult male Syrian hamsters (Mesocricetus auratus) were exposed to one of nine lighting conditions for a duration of 10 weeks: a light-dark cycle of 14 hours of light followed by 10 hours of dark (LD 14:10, a long photoperiod); LD 10:14 (a short photoperiod); a high frequency light-dark cycle of 1 hour of light and 1 hour of dark (LD 1:1); a higher frequency light-dark cycle of 1 minute of light and 1 minute of dark (LD 1m:1m); constant light (LL); constant dark (DD); feedback lighting (LDFB; a condition that illuminates the cage in response to locomotor activity); a feedback lighting neighbor control (LDFB NC; the animal receives the same light pattern as a paired animal in LDFB, but has no control over it); or reverse feedback lighting (rLDFB; a condition that darkens an illuminated cage in response to locomotor activity). Exposure to LL, LD 1:1, LD 1m:1m, LDFB and rLDFB significantly and similarly lengthened the free-running period of the locomotor rhythm when compared to the period of animals in DD. The paired tests and accessory reproductive glands weights, spermiogenesis, seminiferous tubule diameter and serum concentrations of testosterone, prolactin, LH and FSH, suggest that LD 14:10, LL, LD 1:1, rLDFB and LDFB NC maintain reproductive function in the Syrian hamster, while LD 10:14, DD, LD 1m:1m and LDFB do not. It is known that as little as two 1-second pulses of light are stimulatory if coincident with the subjective night (17.22). Thus, it is not surprising that LD 1:1 is stimulatory. LD 1m:1m is not stimulatory, however, despite an identical quanta of light per 24 hours and similar phase relationship. It appears that mere light exposure during the subjective night is not necessarily reproductively inductive. It would also appear that behaviorally generated light-dark cycles can be (i.e., LDFB), but are not necessarily (i.e., rLDFB) inhibitory to the maintenance of the reproductive system in long day breeders. Furthermore, the lighting pattern derived from LDFB is stimulatory if given exogenously (i.e., LDFB NC). Although it is not understood why light exposure that is coincident with the subjective night (i.e., LD 1m:1m and LDFB) is not stimulatory in long day breeders, a possible hypothesis is that an internal coincidence model is involved in the photoperiodic response and that multiple transitions during the subjective night may cause a dissociation of internal oscillations which must be in phase for light to be stimulatory.
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PMID:Nocturnal illumination does not necessarily stimulate the photoperiodic response, despite mimicking the effects of constant light on the circadian system in the male Syrian hamster. 211 74

The Cosmos 1887 biosatellite carried 10 male rats and 2 rhesus monkeys on its 12.5-day mission. Upon re-entry the Vostok vehicle overshot the designated landing site, which resulted in fasting of the animals for 42 h, exposure to cage temperatures of 12-15 degrees C, and 2 days delay in death of the rats. No overt untoward effects of the delayed recovery were apparent. Tissues from the rats were harvested by Soviet scientists, appropriately preserved, and provided to U.S. investigators. Flight rats grew more slowly and had larger adrenal glands than earth gravity controls. Analysis of plasma revealed increased concentrations of hepatic alkaline phosphatase, glucose, urea nitrogen, and creatinine in flight rats. In contrast, electrolytes, total protein, albumin, corticosterone, prolactin, and immunoreactive growth hormone levels were unchanged. However, testosterone concentration was marginally decreased after flight and thyroid hormone levels were suggestive of reduced thyroid function. Due to the possible effects of reentry and the delay in recovery of the animals, it is not clear what relationship postflight levels of plasma constituents bear to their concentrations in flight.
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PMID:Cosmos 1887 mission overview: effects of microgravity on rat body and adrenal weights and plasma constituents. 229 71

This study investigated the effects of long-term, low-level exposure to radio-frequency radiation (RFR) on various physiological systems in a large rodent population. Two hundred adult male white rats with chronically implanted aortic cannulas were randomly divided into two groups. Animals in the first group were exposed to the low-level RFR environment for approximately 22 hours daily, seven days a week, for six months. Depending on animal orientation within the home cage (all animals singly caged) the estimated whole-body specific absorption rate (SAR) ranged from 0.04 to 0.4 W/kg. The estimated mean whole-body SAR ranged from 0.3 W/kg (medium-sized rats) to 0.35 W/kg (large-sized rats). A second, sham-exposure group was maintained under identical conditions, but were not radiated. Microsamples of blood were withdrawn on a cyclic schedule from the unanesthetized and unrestrained rats. The blood samples were assayed for plasma adrenocorticotropin (ACTH), plasma corticosterone, plasma prolactin, plasma catecholamines (norepinephrine, epinephrine, and dopamine), hematological end points (hematocrit ratio, complete red blood cell count, complete white blood cell count, and a differential count of neutrophils, eosinophils, and monocytes), and cardiovascular end points (heart rate and mean arterial blood pressure). Analysis of the results showed no significant RFR-induced differences in these end points when the RFR-exposed group was compared to the sham-exposed group. Chronic exposure to the low-level, pulsed field resulted in no adverse effects on animal health, as measured by the spectrum of blood-borne end points.
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PMID:Long-term study of 435 MHz radio-frequency radiation on blood-borne end points in cannulated rats. Part II: methods, results, and summary. 284 18

Rats were exposed to 15 min of restraint or footshock or forced running in an activity wheel once a day for 10 days. Control groups were handled only. On the 11th day, rats from each stressor group and controls were exposed to 15 min of one stressor in a crossed design such that all combinations of one chronic stressor and one acute stressor were performed. Rats were sacrificed immediately following removal from their home cage or after 15 min stressor exposure on the 11th day and plasma corticosterone and prolactin and pituitary cyclic AMP levels were determined. There were no measured differences in these stress indices among groups of rats sacrificed immediately upon removal from their home cage on day 11 regardless of previous history on days 1 through 10. Plasma corticosterone and plasma prolactin and pituitary cyclic AMP levels were elevated in all rats exposed to any of the three stressors immediately prior to sacrifice as compared to all rats not exposed to stress immediately before sacrifice. However, plasma prolactin and pituitary cyclic AMP responses to each of the 3 stressors were attenuated in rats which had previous exposure to that specific stressor as compared to rats which had previous experience with a different or no stressor. We conclude that habituation results from behavioral experience with a particular stressor rather than biochemical adaptation resulting from repeated challenge to hormonal and neurochemical systems responsive to stress.
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PMID:Habituation to repeated stress is stressor specific. 298 82

Stress-induced renin and prolactin secretion was investigated using a conditioned emotional response paradigm. Three minutes after placement in a chamber the rats received an electric shock to their feet via the grid floor, then were immediately returned to their home cage. This procedure was repeated for 3 consecutive days. On the fourth day, instead of receiving an electric shock, they were removed after 3 min and sacrificed by decapitation. Control rats were treated identically with the exception that shock was not administered at any time. There was a significant increase in plasma renin activity and prolactin level in the stressed rats. The administration of the antianxiety drugs chlordiazepoxide (10 mg/kg i.p.) or midazolam (0.125-2 mg/kg i.p.) blocked the stress-induced increase in prolactin levels but not the stress-induced rise in plasma renin activity. Administration of the beta-blocker propranolol (1 mg/kg i.p.) inhibited, but did not completely block, stress-induced rise in plasma-renin activity and had no effect on stress-induced prolactin secretion. The opiate antagonist naloxone (0.1-10 mg/kg i.p.) and the acetylcholinesterase inhibitor diisopropyl fluorophosphate (0.5 mg/kg i.p.) did not block stress-induced renin or prolactin secretion. It is concluded that stress-induced prolactin secretion is regulated by a benzodiazepine-mediated mechanism and that stress-induced renin but not prolactin secretion is mediated in part via beta-receptors.
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PMID:Pharmacological studies on stress-induced renin and prolactin secretion: effects of benzodiazepines, naloxone, propranolol and diisopropyl fluorophosphate. 299 44

The effects of restraint stress applied at different times of the day on levels of five stress-responsive plasma hormones (ACTH, beta-endorphin, beta-LPH, corticosterone and prolactin) and pituitary cyclic AMP levels were assessed. Different groups of rats were subjected to 15 min of restraint stress at 2-hour intervals over a 24-hour period. Rats were sacrificed immediately upon removal from their home cage (controls) or immediately following restraint (stressed). The time of day of stress exposure markedly affected the stress responses measured. Generally, responses to stress applied at the beginning of the dark cycle (18:00) were less than those seen following stress applied at the beginning of the light cycle (06:00). Stress at 06:00 increased levels of pituitary cyclic AMP 10-fold, while stress applied at 18:00 did not significantly increase pituitary cyclic AMP levels. In stressed rats, high correlations were seen among levels of hormones derived from the common precursor, proopiomelanocortin (ACTH, beta-endorphin, beta-LPH) and between these hormones and levels of pituitary cyclic AMP. These findings support the hypothesis that pituitary cyclic AMP is involved in the stress-induced release or synthesis of the pituitary hormones ACTH, beta-endorphin, and beta-LPH.
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PMID:Diurnal variation in neuroendocrine response to stress in rats: plasma ACTH, beta-endorphin, beta-LPH, corticosterone, prolactin and pituitary cyclic AMP responses. 301 85

The purpose of this study was to correlate behavioral modifications observed in perinatally bromopride-treated animals with possible changes in prolactin (PRL) serum levels. Adult male and female rats perinatally treated with bromopride during pregnancy and/or lactation were used for measuring PRL serum levels. There were no differences in hormone levels between experimental and control groups. The well known sexual dimorphism was observed, i.e. females showed higher levels of PRL than did males. Males of the same cage showed a hormone increase related to the sequence of sacrifice, i.e. the first animals to be sacrificed showed lower PRL levels than did subsequent ones. The possibility raised was that behavioral changes previously observed in rats treated perinatally with bromopride are not related to changes in PRL levels.
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PMID:Prolactin levels in male and female rats perinatally treated with bromopride. 317 68

Experiments were conducted to determine effects of restraint and thermal stressors on plasma prolactin (PRL) in castrated male pigs. A single 20-min restraining period in a restraining cage which prevented both movement and injury increased (P less than 0.05) plasma PRL when applied at either 0800 or 1600 hr. Exposure to 32 degrees C at 0800-1000 hr or at 1600-1800 hr produced more moderate increases (P less than 0.05). A combination of 20 min restraint and 2 hr at 32 degrees C produced a response similar to restraint alone. Twenty minutes after stressor application plasma PRL concentrations in pigs exposed to restraint or restraint +32 degrees C at 1600 h were greater (P less than 0.05) than concentrations measured in all other treatment groups at that time interval. However, there were no statistically significant differences in additional quantitative indices of the plasma PRL responses (maximal level, maximal change, or integrated response above basal levels) among restraint, 32 degrees C, or restraint +32 degrees C, nor between morning and afternoon applications of treatment. Such data do not provide, therefore, any strong evidence for stressor-dependent or circadian differences in plasma PRL response. A second study subjected castrated male pigs to 20 degrees C (controls), 20 +/- 12 degrees C (cyclic temperature, sine wave variation), 5 degrees C constant, and 5 +/- 12 degrees C cyclic for 20 days. After 6 days exposure to 5 degrees C constant or 5 +/- 12 degrees C cyclic there were decreases (P less than 0.05) of 59 and 67% respectively in plasma PRL when compared either with pretreatment levels or with levels in pigs at 20 or 20 +/- 12 degrees C. There were no differences in PRL responses between cyclic vs constant temperatures. These results are the first to indicate that plasma PRL in pigs is affected by acute restraint and thermal stressors.
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PMID:Stressor-associated alterations in porcine plasma prolactin. 342 19


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