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1.
Mech Ageing Dev ; 102(2-3): 263-77, 1998 May 15.
Article in English | MEDLINE | ID: mdl-9720657

ABSTRACT

Previous studies show that fast exploration of a T-shaped maze by mature mice may predict an above average longevity. Since the nervous and the immune systems work in a coordinated fashion, and it seems that these two homeostatic systems both influence organismic aging and suffer a senescent decline, we have performed a comparative study of the above behavioral parameter and different functions of three representative immune cells: lymphocytes, macrophages and natural killer (NK) cells obtained from old (76 +/- 1 weeks of age) female OF1-Swiss mice. At 70 weeks of age the mice were divided into a 'fast' and a 'slow' group, containing 100 and 0%, respectively, of animals able to explore the 50 cm-long first arm of the maze in 20 s or less. At 76 +/- 1 weeks of age the animals were sacrificed, the peritoneal cell suspensions were obtained and the immune organs (axillary nodes, spleen and thymus) were isolated. The following leukocyte functions were studied in peritoneal macrophages: adherence to substrate, mobility (spontaneous and chemotaxis), ingestion of particles and superoxide anion production whereas mobility, lymphoproliferative response to the mitogen Con A and NK activity were studied in the immune-organ leukocyte suspensions. The results show that the aged fast mice have better immune functions than the aged slow mice.


Subject(s)
Aging/physiology , Killer Cells, Natural/physiology , Macrophages, Peritoneal/physiology , Aging/immunology , Animals , Female , Mice , Superoxides/metabolism
2.
Mech Ageing Dev ; 102(2-3): 249-61, 1998 May 15.
Article in English | MEDLINE | ID: mdl-9720656

ABSTRACT

The general immunodepression found in ageing organisms may be related to changes in the neuroimmune network. In the present study, the migration capacity of lymphocytes from BALB/c mice of three different ages: young (12 +/- 2 weeks), adult (24 +/- 2 weeks) and old (72 +/- 2 weeks), has been assayed in vitro in response to three neuropeptides: sulfated cholecystokinin octapeptide (CCK-8s), gastrin-releasing peptide (GRP) and neuropeptide Y (NPY) in a physiological range of concentrations (10(-8)-10(-12) M). The capacity of migration to a chemical gradient or chemotaxis was studied by the Boyden's technique using f-met-leu-phe at 10(-8) M as chemoattractant. The results show a different response of lymphocytes to the different neuropeptides, as wells as to age, concentrations and locations studied. However, some similarities were found, for instance the three neuropeptides inhibited chemotaxis in thymus. The stimulatory effects that GRP and NPY exerted in young and adult mice were not observed in old animals. CCK-8s inhibited the chemotaxis in every organ studied, with the effect being more striking in old mice. Our conclusion is that stimulatory effects of the neuropeptides disappear or become inhibitory with ageing.


Subject(s)
Aging/physiology , Chemotaxis, Leukocyte/physiology , Gastrin-Releasing Peptide/metabolism , Neuropeptide Y/metabolism , Receptors, Cholecystokinin/metabolism , Sincalide/analogs & derivatives , T-Lymphocytes/physiology , Animals , Chemotaxis, Leukocyte/drug effects , Gastrin-Releasing Peptide/pharmacology , Male , Mice , Mice, Inbred BALB C , Neuropeptide Y/pharmacology , Sincalide/metabolism , Sincalide/pharmacology , T-Lymphocytes/drug effects
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