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Biomedical subjects

M Petersson

Publications and source records attributed to M Petersson.

56 records · Page 4Linked to original sources

Dissociation of oxytocin effects on body weight in two variants of female Sprague-Dawley rats.

As a counterpoint to studies that make a case for the use of oxytocin in short-term inhibition of food intake, the aim of the present study was to determine whether the peptide facilitates weight gain in female rats in a more long-term perspective. Two different variants of females Sprague-Dawley rats were used. The two variants differed in daily weight gain (0.38 g/day vs. 1.41 g/day during 28 days), and were designated slowly and rapidly growing rates (SGR and RGR) respectively. Oxytocin 1 mg/kg given s.c. to SGR for a five-day period increased weight gain significantly in comparison to a previous five-day period with NaCl-treatment (18.0 g/5 days versus 5.0 g/5 days; p < 0.01). In a separate study, oxytocin 1 mg/kg given for four days increased weight gain significantly in SGR versus saline-treated controls (7.5 g/4 days versus 1.6 g/4 days; p < 0.05). The weight-difference persisted six days later (p < 0.001). The weight increase of oxytocin occurred only during estrus (p < 0.05) and was not accompanied by any measurable increase in food intake. In RGR, oxytocin-treatment decreased food intake significantly (p < 0.001) and tended to decrease weight gain, although not significantly. The SGR and RGR also had different endocrine profiles with, for example, twice as high oxytocin (p < 0.01) and insulin levels (p < 0.01) in RGR compared to the SGR. These data suggest that oxytocin influences weight gain and food intake differently in the two variants of Sprague-Dawley rats, perhaps depending on factors such as endocrine profile and oxytocin sensitivity.

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Non-lytic pre-NK cells are enriched in the spleen as a result of long-term depletion of mature NK cells with anti-NK-1.1 monoclonal antibody.

In this study, we wanted to establish a new model as an alternative to bone marrow, where non-lytic pre-NK cells can be further studied with respect to phenotype and relation to other haematopoietic cell lineages. B6 mice were depleted of mature NK cells by either weekly injections from birth, or a single injection as adults, with the monoclonal antibody anti NK-1.1, and the frequency of interleukin-2 (IL-2)-responding cells (as determined by cytotoxicity or proliferation) was investigated. By comparing the frequency of IL-2-induced cytotoxic cells between NK-1.1(-) mice depleted from NK cells by a single injection with those depleted from birth, we observed a 3-fold higher frequency in mice depleted from birth [1/(11,941 +/- 30) vs. 1/(29,903 +/- 104)]. Non-lytic pre-NK cells were further enriched by selective in vitro depletion of sIg+, CD4+ and CD8+ cells. In this non-B, non-T spleen cell population the frequency of cells proliferating in response to 7 days culture with IL-2 or IL-3 was 2-fold higher in NK-1.1(-) mice than in control mice [1/(4,340 +/- 27) vs. 1/(9,250 +/- 67) and 1/(3,370 +/- 41) vs. 1/(7,610 +/- 50), respectively]. We conclude that NK depletion from birth results in an enhanced frequency of pre-NK cells, and propose this as a model to further study the identity of the progenitor and pre-NK cell.

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