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M L Walsh

Publications and source records attributed to M L Walsh.

At least 19 recordsLinked to original sources

Cohabitation with a sterile male facilitates the development of retrieval behavior in nulliparous female rats exposed to pups.

Female rats were housed with a sterile male or another female. After 3 weeks, half of the females that had been housed with a female were rehoused with an intact male. At the end of 6 weeks female or sterile male cagemates were removed. Intact male cagemates and pups were removed 3 to 12 h following parturition. All females were tested for retrieval of three unfamiliar pups placed in their cage on the day following removal of their cagemate. Three unfamiliar pups were placed with each female and the female's behavior observed for 10 min. Observations were made in this way for 13 days or until the female retrieved all three pups within the 10-min interval. Pups were left with the female on days they were not retrieved. Females housed with a sterile male reached criterion for pup retrieval in 2.9 days, significantly fewer days than were required for females housed with another female (6.6 days) but significantly more than were required for a postpartum female (0.8 days). By demonstrating that cohabitation with a male fosters the development of retrieval, these results support evidence from the study of aggressive behavior that pseudopregnancy facilitates the development of behaviors associated with pregnancy and lactation.

Aggression

Interaction of estradiol, testosterone, and progesterone in the modulation of hormone-dependent aggression in the female rat.

Female rats that had become aggressive as a result of cohabiting with a sterile male were ovariectomized and implanted with Silastic tubes of estradiol, testosterone, and progesterone, estradiol and testosterone alone, or with empty tubes. The implants were designed to model serum concentrations present during the last week of pregnancy (estradiol, 0.06 ng/ml; testosterone, 2.6 ng/ml; progesterone, 70 ng/ml). Following a test of aggression 1 week postoperatively, estradiol and testosterone implants were replaced with ones designed to maintain the lower hormone levels present following parturition (0.02 ng/ml; 0.6 ng/ml, respectively). Progesterone was not replaced. At the first aggression test, females with estradiol and testosterone alone displayed significantly more aggression than females with these hormones plus progesterone. Both groups were more aggressive than females without hormone replacement. Following the exchange of large implants for small ones, females that previously had progesterone increased in aggression while females that previously had only estradiol and testosterone decreased in aggression. Both groups continued to be more aggressive than the group without hormone replacement. High serum progesterone present near the end of pregnancy appears to moderate the expression of aggression supported by estradiol and testosterone. Conversely, progesterone's decline at parturition appears to produce a rebound facilitation of aggression even though serum estradiol and testosterone simultaneously decline.

Aggression

Ovariectomy does not attenuate aggression by primiparous lactating female rats.

Nulliparous female hooded rats were allowed to cohabit with a sexually active male in a large living cage. Aggression toward an unfamiliar female was assessed during the second and third week of pregnancy. Within 12 to 24 h following parturition females were ovariectomized (n = 7) or sham-ovariectomized (n = 6) in a manner that balanced previous aggression scores. Aggression was assessed at 48 h following ovariectomy and at three weekly intervals thereafter. Ovariectomized and sham-ovariectomized females did not differ in the number of attacks, number of bites, duration of on-top, or frequency of piloerection on any test day following parturition. These results indicate that circulating levels of ovarian steroids do not influence the level of aggression by a primiparous lactating female toward an unfamiliar female conspecific.

Aggression

Hormone-dependent aggression in male and female rats: experiential, hormonal, and neural foundations.

Hormone-dependent aggression in both male and female rats includes the distinctive behavioral characteristics of piloerection and lateral attack. In males the aggression is dependent on testicular testosterone and is commonly known as intermale aggression. In females, the aggression is most commonly observed as maternal aggression and is dependent on hormones whose identity is only beginning to emerge. The present review examines the experiential events which activate hormone-dependent aggression, the relation of the aggression to gonadal hormones, and the neural structures that participate in its modulation. In males and females, the aggression is activated by cohabitation with a conspecific of the opposite sex, by competitive experience, and by repeated exposure to unfamiliar conspecifics. In the female, the presence of pups also activates aggression. In both males and females, hormones are necessary for the full manifestation of the aggression. The essential hormone appears to be testosterone in males and a combination of testosterone and estradiol in females. The information available suggests the neural control systems for hormone-dependent aggression may be similar in males and females. It is argued that hormone-dependent aggression is behaviorally and biologically homologous in male and female rats.

Aggression

A thermoluminescent dosimetry intercomparison in operational power station fields.

A dosimetry intercomparison was held among the five agencies in Canada that are recognized by the Atomic Energy Control Board as competent to perform external dosimetry. Exposures of thermoluminescent dosimeter badges were made under operational conditions to radiation fields in Candu nuclear generating stations. Details of the method are described including the large, block-type phantoms (with a rotating front face so that all badges were equally exposed) and a small device to measure the depth-dose distribution. Thirty-six exposures (or "runs") were made, exposing 522 badges for periods of 1 h-2 d. Normalization between the runs was based on the absorbed dose at 1,000 mg cm-2 for each run, as measured by the depth-dose device. Using this method, the average relative readings for the five participants ranged from 1.01-1.40 (dimensionless).

Canada

Possible mechanisms of oxygen uptake kinetics.

The VO2 response to a step change in work rate resembles a first order exponential function. This suggests that a single site of the many which link ATP demand to VO2 is limiting. The location of this site is controversial. Some authors suggest that O2 delivery regulates the VO2 response. Others have suggested that peripheral mechanisms within the active muscle regulate O2 consumption. The evidence supporting each hypothesis is reviewed. It is concluded that O2 delivery sets the initial parameters and peripheral mechanisms then regulate O2 utilization within the bounds initially established by delivery mechanisms.

Humans

The clearance rate of exercise-elevated blood lactate following physical training.

In this paper, previous studies regarding the effect of physical training on the disappearance rate of blood La during recovery after strenuous exercise have been briefly summarized. The results of our own recent study of this problem have also been added. It may be concluded that there is some evidence for an improved lactate metabolic clearance rate resulting from physical training in human subjects, when the degradation rate is estimated from serial blood samples taken during a standard ramp ergometer test to exhaustion during each week of a training/detraining sequence. This beneficial effect of training, however, may also be influenced by the initial physical status of the subject and the nature of the training program.

Exercise

Exercise breathing pattern during chronic altitude exposure.

Breathing pattern in response to maximal exercise was examined in four subjects during a 7-day acclimatisation to a simulated altitude of 4247 m (barometric pressure, PB = 59.5 kPa). Graded exercise tests to exhaustion were performed during normoxia (day 0), and on days 2 and 7 of hypoxia, respectively. Ventilation was significantly augmented in the hypoxic environment, as were both the mean inspiratory flow (VT/TI) and inspiratory duty cycle (TI/TTOT) components of it. VI/TI was increased due to a significant increase in tidal volume (VT) and a corresponding decrease in inspiratory time duration (TI). Throughout a range of exercise ventilation, TI/TTOT was increased due to an apparently greater decrease in expiratory time duration (TE) with respect to TI. In all cases, the relation between VT and TI displayed a typical range 2 behaviour, with evidence of a range 3 occurring at very high ventilatory rates. There was essentially no difference observed in the VT-TI relation during exercise between the normoxic and hypoxic conditions. No significant changes were observed in the breathing pattern in response to exercise within the exposure period (from day 2 to day 7), although there was a discernible tendency to a higher stage 3 plateau by day 7 of altitude exposure.

Acclimatization

Serum estradiol concentration required to maintain body weight, attractivity, proceptivity, and receptivity in the ovariectomized female rat.

Female hooded rats (230 to 260 g) were ovariectomized and given a subcutaneous implant of an estradiol-filled Silastic tube. The length of the tube was varied in order to produce a variety of serum estradiol levels. In the first experiment, animals were weighed over a 6-week period following surgery and then tested for sexual responsiveness to a male. The results demonstrated that ovariectomized females with an implant maintaining a serum estradiol concentration at about 15 pg/ml maintained body weight at the same level as that of intact females. A smaller implant gave rise to a higher weight gain and a larger implant to a lower weight gain. All implants resulted in a continuous state of receptivity. In a second experiment, ovariectomized females were implanted with smaller estradiol-filled implants in order to determine the threshold for maintaining proceptivity and receptivity. The results indicated that with a serum estradiol concentration below 15 pg/ml, the frequency of lordosis and of ear wiggling and darting decreased. Progesterone injections facilitated both proceptive and receptive behavior. In addition, following progesterone injections, the time required for a male to mount a female 10 times was decreased in females with low or no estradiol replacement. These results indicate that a constant concentration of estradiol at about the mean level present throughout the estrous cycle will result in normal body weight regulation and will maintain sexual behaviors that normally occur only during estrus. These results emphasize that Silastic implants of estradiol do not mimic normal endocrine function since, even at low levels, estradiol implants produce continuous receptivity.

Animals

Enhanced defensiveness and increased food motivation each contribute to aggression and success in food competition by rats with medial hypothalamic lesions.

Castrated male rats (N = 27) with medial hypothalamic lesions or sham lesions were placed on a 23-h food-deprivation schedule and adapted to a highly palatable liquid food. They were also given two tests of defensiveness toward an experimenter. All animals were then housed in medial hypothalamic lesion/sham lesion pairs and subjected to a series of 6 competition tests (1 per day). Following the competition tests, all animals were given individual food consumption tests and a third test of defensiveness toward an experimenter. Correlational analysis showed that postcompetition defensiveness scores but not precompetition defensiveness scores or individual food consumption were related to aggression during the food competition. Analysis by criterion groups indicated that animals high in precompetition defensiveness and with food consumption in the normal range were not more successful in the competition but were slightly more aggressive than their sham-lesioned competitors. Animals with high postcompetition defensiveness scores and with individual food consumption in the normal range were more successful than their sham-lesioned competitors and the most aggressive of the lesioned animals during the food competition. Animals that were high in food consumption and only moderately defensive were also more successful but only slightly more aggressive in the food competition than their sham-lesioned competitors. These results suggest that a high and stable level of defensiveness, and excessive food intake, each contribute to the success and aggressiveness of rats with medial hypothalamic lesions in a food competition situation.

Aggression

Hormone-dependent aggression in the female rat: testosterone plus estradiol implants prevent the decline in aggression following ovariectomy.

Female rats were individually housed with a sterile male for the duration of the experiment. Beginning 7 to 10 weeks after the start of cohabitation, each female was tested for aggression toward an unfamiliar female at weekly intervals for 3 weeks. Females that displayed consistent and substantial aggression were given one of the following treatments: ovariectomy followed by both testosterone and estradiol implants, ovariectomy followed by 2 empty implants, or sham ovariectomy followed by 2 empty implants. The implants were subcutaneously placed hormone-filled Silastic capsules. They were expected to produce a serum testosterone concentration of 0.5 ng/ml and an estradiol concentration of 15 pg/ml. Postoperatively, the aggression of each female continued to be assessed on a weekly basis for 3 weeks. Ovariectomized females with hormone implants displayed a level of aggression postoperatively similar to that of sham-ovariectomized females and significantly greater than that of ovariectomized females with empty implants. These results, together with others, suggest that estradiol and testosterone act together to form the hormonal foundation of hormone-dependent aggression by females cohabiting with a sterile male.

Aggression

Aggression by a female rat cohabitating with a sterile male: termination of pseudopregnancy does not abolish aggression.

At the end of that time, each female was assessed for aggressiveness toward an unfamiliar female intruder once each week for 3 weeks. Those females displaying a high level of aggression had their male cagemate changed. For half of the females, the new male cagemate was a castrated male with a testosterone implant. For the other half, the new cagemate was a castrated male without a testosterone implant. Replacement males had been subjected to surgery 9 weeks previously. There were no differences in the aggressiveness of females of the two groups on any of 3 subsequent weekly tests of aggression. In a 3-h evaluation of male sexual behavior, none of the 9 castrated males without testosterone replacement displayed sexual activity with an estrogen/progesterone primed ovariectomized female, but 6 of 9 males with testosterone replacement did. Reanalysis of the aggression data comparing the females whose males had no testosterone replacement and females housed with the 6 males that were sexually active also revealed no differences in aggression over the 21-day test period. Since pseudopregnancy is known to last 13 days, these results indicate that the continuous presence of pseudopregnancy is not required for maintenance of aggression by a female cohabiting with a sterile male.

Aggression

Hazard assessment of video display units.

This report describes the results of a study of potential health hazards of video display units (VDUs). The specific elements of the study included characterizing the emissions of ionizing and nonionizing radiation and exposures to electromagnetic fields. There was no evidence that operators are exposed to electric, magnetic, or ionizing radiation fields significantly above ambient levels. Significant x-ray leakage cannot occur under any credible conditions. In addition to the ergonomic aspects of VDU work, reports on the health aspects of VDU operators were investigated. The results of the study, based on the specific hazards evaluated, do not support allegations that VDU operation is hazardous beyond the identified transient discomforts associated with characteristics of the work performed. A high-profile employee education program was initiated to minimize discomforts and unwarranted concerns.

Air Pollutants, Radioactive

Update on antimicrobial agents.

A variety of antimicrobial agents are currently in use to treat bacterial, fungal, and viral infections. Pharmacologic and microbiologic properties unique to the classes of drugs are reviewed in this article. Home parenteral antibiotics are an acceptable and efficacious way to treat certain infections and may lead to shorter hospitalizations. Knowledge of general drug characteristics, indications, and toxicities will help the nurse to manage effectively the patient receiving antimicrobial therapy.

Anti-Bacterial Agents

Aggression by ovariectomized female rats: combined testosterone/estrogen implants support the development of hormone-dependent aggression.

Female hooded rats were ovariectomized and implanted with a single estrogen-filled and a single testosterone-filled Silastic tube. Control animals were ovariectomized and implanted with empty tubes. The implants produced an estrogen concentration of 30 pg/ml and a testosterone concentration of 0.25 ng/ml, levels close to those found in intact females. Two weeks following surgery, all animals were housed in individual cages, placed on a 23-hr food-deprivation schedule, and adapted to a liquid food. They were then housed in hormone-implant/empty-implant pairs and given a series of 3 restricted-access competition tests and 3 free-access competition tests (1/day). The animals were then paired with new partners and given a second series of restricted-access and free-access competition tests. Ovariectomized females with hormone implants were more successful at maintaining access to the liquid food and more aggressive than their competitors without hormone replacement. The aggression was used to maintain access to food during free-access as well as restricted-access competition. Following the competition tests, animals with hormone implants were significantly more aggressive toward an unfamiliar conspecific than were their cagemates with empty implants. The level of success and aggression by females with testosterone + estrogen implants appears greater than that which occurs with either hormone alone and comparable to that observed in intact females.

Aggression

Hormone-dependent aggression in female rats: testosterone implants attenuate the decline in aggression following ovariectomy.

Female rats were individually housed with a sterile male for a 4- to 5-week period. Each female was then tested for aggression toward an unfamiliar female intruder at weekly intervals. Those females that displayed a high level of aggression on each of three weekly tests were ovariectomized and given subcutaneous implants of testosterone-filled tubes, ovariectomized and given subcutaneous implants of empty tubes, or sham-ovariectomized and implanted with empty tubes. These implants should produce a serum testosterone concentration of about 0.6 ng/ml, compared to 0.17 ng/ml in intact females. Beginning 1 week postoperatively, the aggression of each female was tested weekly for 4 weeks. Ovariectomized females with testosterone implants displayed a level of aggression significantly higher than that of ovariectomized females with empty implants on 3 of 4 weekly tests. The level of aggression by females with testosterone implants was not significantly different from that of sham-ovariectomized females on the first postoperative test. Additional observations showed that testosterone implants did not produce an increase in aggression in females whose preoperative level of aggression was low. Further, Silastic implants containing estrogen (1 to 2 mm long) sufficient to maintain a serum estrogen level of 20 to 30 pg/ml also attenuated the decline of aggression following ovariectomy. These results suggest that testosterone and estrogen may both contribute to the biological substrate of hormone-dependent aggression in female rats.

Aggression

Aggression by ovariectomized female rats with testosterone implants: competitive experience activates aggression toward unfamiliar females.

Female hooded rats (250 to 325 g) were ovariectomized and bilaterally implanted with testosterone-filled or empty Silastic tubes. The testosterone-filled space in each tube was 10 mm long and this should produce a serum testosterone concentration 4 to 5 times that of an intact female, but well below that of a male. Three weeks following surgery, half of the animals with testosterone implants were housed with an animal with an empty implant and left for 6 weeks. The remaining animals were placed on a 23-hr food deprivation schedule, housed in testosterone implant/empty implant pairs, and then subjected to a series of food competition tests. Following the competition tests, all animals were individually tested in their living cage for aggression toward an unfamiliar female. In food competition, females with testosterone implants were more successful and more aggressive than their cagemates with empty implants. When tested for aggression toward an unfamiliar intruder, females with testosterone implants given competitive experience were more aggressive toward an intruder than were their cagemates with empty implants or females with testosterone implants not given the competitive experience. Females with testosterone implants but without competitive experience were not more aggressive toward an unfamiliar female than were their cagemates with empty implants. These results suggest that, in ovariectomized females with testosterone implants, hormone-dependent aggression fostered by a competitive situation is displayed toward unfamiliar females.

Aggression