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L Moffatt

Publications and source records attributed to L Moffatt.

9 recordsLinked to original sources
PubMed2001

Metabolic rate and thermal stability during honeybee foraging at different reward rates.

During honeybee foraging, the stabilization of thoracic temperature (Tth) at elevated values is necessary to meet the power requirements of flight at different air temperatures (T(a)). To understand how the bee achieves thermal stability at different reward rates, the metabolic rates of undisturbed foraging bees were measured at different T(a) values and different sucrose solution flow rates. Metabolic heat production, calculated from the rate of carbon dioxide production, decreased linearly from 49.7 to 23.4 mW as T(a) increased from 19 to 29 degrees C (sucrose flow rate 1.75 microl x min(-1), 50 % w/w). In contrast, crop load and inspection rate remained constant. Metabolic rate displayed a linear relationship with both T(a) and the logarithm of the flow rate of sucrose solution (range analyzed 0.44-13.1 microl x min(-1), 50 % w/w). Metabolic rate decreased by 3.13+/-0.52 mW (mean +/- s.e.m., N=37) for every 1 degrees C increase in T(a) and increased by 4.36+/-1.13 mW for a doubling in flow rate. These changes in metabolic power output might be used to achieve thermal stability during foraging. It is suggested that the foraging bee might increase its Tth in accordance with the reward rate.

Animals↗
PubMed2000

Changes in the metabolic rate of the foraging honeybee: effect of the carried weight or of the reward rate?

The metabolic rate of free flying honeybees (Apis mellifera ligustica) foraging on a multiple automatic feeder was measured in complete absence of perturbation. Each time the sucrose flow rate was doubled, the metabolic rate increased by 18.2 +/- 2.0% (14.7 microl CO2 min(-1) and final crop load by 25.1 +/- 2.4% (7.04 microl). The possibility that the heavier load carried by the bees caused the increase in the metabolic rate was analyzed in detail. It was found that, for the same weight in the crop, the metabolic rate increased with the increasing reward rate. Therefore, a factor other than the carried weight might account for this increase: a motivational drive, whose intensity may depend on the reward rate at the food source. Although at higher reward rates metabolic rate increased during the visit, at lower reward rates it remained constant, suggesting that the effect of the carried weight on the metabolic rate might be controlled by this motivational drive. The hypothesis that honeybees maximize individual efficiency by reducing their crop load loses support, as foraging costs are not determined by the carried weight. The functional meaning of the reduction in crop load would be to increase the informational exchange at the hive.

Animals↗
PubMed1997

Oxygen consumption in the foraging honeybee depends on the reward rate at the food source.

Oxygen consumption of the honeybee Apis mellifera ligustica was measured as a function of the flow rate supply of sucrose solution at an automatic feeder located inside a respirometric chamber. Trained bees freely entered the respirometric chamber and collected the sucrose solution supplied. The mean value of the O2 consumption rate per visit increased with the sucrose flow rate, and for a given flow rate, with increasing locomotor activity. However, when no locomotor activity was displayed, O2 consumption also increased with increasing nectar flow rate. Crop load attained at the end of the visit showed a positive relationship with the nectar flow rate; however, for a given flow rate, O2 consumption showed either no correlation or a negative one with the final crop load attained. It is concluded that the energy expenditure of the foraging bee is controlled by a motivational drive whose intensity depends on the reward rate at the food source.

Animals↗
PubMed1992

Development of fetal thymocytes in organ culture: effect of corticosteroids.

Corticosteroids affect the development of fetal foregut-derived organs in which epithelial-mesenchymal interactions are associated with the developmental process. The thymus is one such organ and is profoundly sensitive to corticosteroids when mature. In this study corticosterone (CS) effects on fetal thymocyte development were investigated using a fetal thymus organ culture system which allows the growth, differentiation, and function of developing thymocytes to be monitored in vitro. CS inhibited, but did not block growth of fetal thymocytes, although the appearance of mature thymocytes was inhibited, similar to previously reported effects of interleukin 2 (IL2). CS enhanced the proportion of Mac1+, Ia+ and FcR+ cells and maintained high levels of IL2 receptor (IL2R) positive immature cells. Functional cytotoxic cells were detected in CS-treated organ cultures which expressed a Thy 1-, CD8- phenotype, atypical for thymus derived killer cells. While this cytotoxicity may be stimulated by CS, it could simply be due to a relative depletion of the main pool of thymocytes. These cytotoxic cells may have a role in directing apoptotic mechanisms occurring during thymocyte development.

Adrenal Cortex Hormones↗
PubMed1989

Development of thymocytes in organ culture: migrant cells with natural killer cell characteristics.

During organ culture of foetal thymic lobes, up to 5% of the thymic cells migrate out of the lobes and a majority of these have phenotypic characteristics of thymocytes or macrophages. Interleukin-2 (IL-2) increases the number of these migrant cells, and cytotoxic cells can be detected which display natural killer cell surface markers. In contrast, although cytotoxic activity can be detected in cells from adult thymic fragments cultured with IL-2, the cytotoxic activity is not detected with natural killer sensitive target cells. The appearance of natural killer-like cells during the culture of foetal thymic lobes suggests that they are involved in differentiation events which occur at this time in the thymus.

Animals↗
PubMedDate not supplied

Arginine supplementation is well tolerated but does not enhance mitogen-induced lymphocyte proliferation in elderly nursing home residents with pressure ulcers.

BACKGROUND: Immune function declines with age, increasing risk for infection and delaying wound healing. Arginine enhances immune function and healing of standardized wounds in healthy elderly persons. The purpose of this study was to determine what level of arginine supplementation was orally and metabolically tolerated and effective in enhancing immune function in elderly persons with pressure ulcers. METHODS: Residents with one or more pressure ulcers were recruited from two local nursing homes. Subjects were randomized to receive 0 g (n = 10; age, 82 +/- 3 years), 8.5 g (n = 11; 81 +/- 3 years), or 17 g (n = 11; 87 +/- 2 years) of supplemental arginine each day for 4 weeks. Oral tolerance, ie, absence of nausea, vomiting, abdominal distention, or diarrhea, was assessed daily. Metabolic tolerance was assessed weekly by evaluating serum electrolytes. Lymphocyte proliferation to phytohemagglutinin and interleukin 2 production were measured at baseline and after 4 weeks of supplementation as indicators of immune function. RESULTS: Supplemental arginine significantly increased plasma arginine levels and was orally and metabolically tolerated with no complaints of abdominal distress or no clinically relevant changes in electrolyte levels among groups. Lymphocyte proliferation and interleukin 2 production were significantly different between nursing homes. When data from nursing homes were considered individually, arginine supplementation did not enhance the proliferative response. In subjects from nursing home 2 only, there was a 38% and 75% decrease (p < .05) in lymphocyte proliferation with 8.5 and 17 g of supplemental arginine, respectively. Interleukin 2 production was no different among supplementation groups. CONCLUSIONS: Pharmacologic doses of arginine were well tolerated but did not enhance lymphocyte proliferation or interleukin 2 production in nursing home residents with pressure ulcers. CLINICAL RELEVANCY: Enteral formulas supplemented with pharmacologic levels of arginine are frequently administered to elderly persons. This study demonstrates that the very old can tolerate these nitrogen loads if baseline renal function is normal and fluid intake is encouraged. Further research needs to be completed investigating the effect of arginine supplementation on immune function in this population before recommending arginine use.

Administration, Oral↗
PubMedDate not supplied

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