Combined effect of obesity and aging on feeding-induced monoamine release in the rostromedial hypothalamus of the Zucker rat

International Journal of Obesity

Volumn 22, Issue 10, 1998, Pages 993-999

  Lemierre, S ^a   Rouch, C ^a   Nicolaidis, S ^a   Orosco, M ^a,b  

^a l'alimentation et l'Environnement   (France)

^b EUROPEAN SPACE AGENCY   (France)

Author keywords

Aging; Dopamine; Hypothalamus; Microdialysis; Serotonin; Spontaneous feeding; Zucker rats

Indexed keywords

DOPAMINE; MONOAMINE; NEUROTRANSMITTER; SEROTONIN;

ANIMAL EXPERIMENT; ARTICLE; FEEDING BEHAVIOR; HYPOTHALAMUS; LONGEVITY; MALE; MICRODIALYSIS; MONOAMINE RELEASE; NONHUMAN; OBESITY; PRIORITY JOURNAL; RAT; SATIETY; SENESCENCE;

EID: 0031684918     PISSN: 03070565     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ijo.0800717     Document Type: Article

References (54)

1. Grossman SP. Eating or drinking elicited by direct adrenergic or cholinergic stimulation of hypothalamus. Science 1960; 132: 301-302.
2. Hoebel BG. The pharmacology of feeding. In: Iversen LL, Iversen SD, Snyder SH (eds). Handbook of Psychopharmacology. Plenum Press: New York, 1977, pp 55-129.
3. Blundell JE. Serotonin and appetite. Neuropharmacology 1984; 23: 1537-1552.
4. Garattini S, Caccia S, Mennini T, Samanin R, Consolo S, Ladinsky H. Biochemical pharmacology of the anorectic drug fenfluramine: A review. Curr Med Res Opin 1979; 1 (suppl 6): 15-27.
5. Leibowitz SF, Shor-Posner G. Brain serotonin and eating behaviour. Appetite 1986; 7: 1-14.
6. Samarin R, Mennini T, Garattini S. Evidence that it is possible to cause anorexia by increasing release and/or directly stimulating postsynaptic serotonin receptors in the brain. Prog Neuropsychopharmacol 1980; 4: 363-369.
7. Leibowitz SF, Rossakis C. Pharmacological characterization of perifornical hypothalamic dopamine receptors mediating feeding inhibition in the rat. Brain Res 1979; 172: 115-130.
8. Orosco M, Nicolaidis S. Spontaneous feeding-related monoaminergic changes in the rostromedial hypothalamus revealed by microdialysis. Physiol Behav 1992; 52: 1015-1019.
9. Bray GA, York D. Genetically transmitted obesity in rodents. Physiol Rev 1971; 51: 598-646.
10. Dilettuso BA, Wangsness PJ. Effect of age on hyperphagia in the genetically obese Zucker rat. Proc Soc Exp Biol Med 1977; 154: 1-5.
11. Becker EE, Grinker J. Meal patterns in the genetically obese Zucker rat. Physiol Behav 1977; 18: 685-691.
12. Castonguay TW, Upton DE, Leung MB, Stern JS. Meal patterns in the genetically obese Zucker rat: A reexamination. Physiol Behav 1982; 28: 911-916.
13. Levin BE, Sullivan AC. Catecholamine levels in discrete brain nuclei of seven month old genetically obese rats. Pharmacol Biochem Behav 1979; 11: 77-82.
14. Orosco M, Trouvin JH, Cohen Y, Jacquot C. Ontogeny of brain monoamines in lean and obese female Zucker rats. Physiol Behav 1986; 36: 853-856.
15. Tsuji S, Nakai Y, Fukata J, Nakaishi S, Takahashi H, Usui T, Imura H, Ikeda H, Matsuo T. Monoamine metabolism and its response to food deprivation in the brain of Zucker rats. Physiol Behav 1988; 44: 495-500.
16. Orosco M, Rouch C, Meile MJ, Nicolaidis S. Spontaneous feeding-related monoamine changes in rostromedial hypothalamus of the obese Zucker rat: a microdialysis study. Physiol Behav 1995; 57: 1103-1106.
17. Phillips MS, Liu Q, Hammond HA, Dugan V, Caskey CT, Hess JF. Leptin receptor missense mutation in the fatty Zucker rat. Nat Genet 1996; 13: 18-19.
18. Cusin I, Rohner-Jeanrenaud F, Stricker-Krongrad A, Jeanrenaud B. The weight-reducing effect of an intracerebroventricular bolus injection of leptin in genetically obese fa/fa rats. reduced sensitivity compared to lean animal. Diabetes 1996; 45: 1146-1150.
19. Stephens TW, Basinksi M, Bristow PK, Bue-Valleskey JM, Burgett SG, Craft L, Hale J, Hoffmann J, Hsiung HM, Kriauclunas A, MacKellar W, Rostock PR, Schoner B, Smith D, Tinsley FC, Zhang XY, Helman M. The role of neuropeptide Y in the antiobesity action of the obese gene product. Nature 1995; 377: 530-532.
20. Costa A, Poma A, Martignoni E, Nappi G, Ur E, Grossman A. Stimulation of corticotrophin-releasing hormone release by the obese (ob) gene product, leptin, from hypothalamic explants. Neuroreport 1997; 8: 1131-1134.
21. Myers RD, Lankford MF, Paez X. Norepinephrine, dopamine and 5-HT release from perfused hypothalamus of the rat during feeding induced by Neuropeptide Y. Neurochem Res 1992; 17: 1123-1132.
22. Shimizu H, Bray GA. Modulation by corticotrophin-releasing factor of monoamine metabolism in the lateral hypothalamus. Neurosci Lett 1989; 103: 74-80.
23. Matson CA, Wiater MF, Kuijper JL, Weigle DS. Synergy between leptin and cholecystokinin (CCK) to control daily caloric intake. Peptides 1997; 18: 1275-1278.
24. Voigt JP, Sohr R, Fink H. CCK-8S facilitates 5-HT release in the rat hypothalamus. Pharamcol Biochem Behav 1998; 59: 179-182.
25. Newby FD, Digirolamo M, Costonis GA, Kutner MH. Model of spontaneous obesity in aging male Wistar rats. Am J Physiol 1990; 259: R1117-R1125.
26. Duhault J, Lacour F, Boulanger M, Della-Zuana O, Ravel D, Wierzbicki M, Espinal J. S15261, a new compound for the treatment of the insulin resistance syndrome. Diabetologia 1994; 37: 969-975.
27. Bray GA. The Zucker fatty rat: a review. Federation Proc 1977; 36: 148-153.
28. Zucker LM, Antoniades HN. Insulin and obesity in the genetically obese rat 'fatty'. Endocrinology 1972; 90: 1320-1330.
29. Rietveld WJ, Ruis J, Buijs P. The effect of ageing on the circadian control of food intake in the rat. J Interdiscipl Cycle Res 1988; 19: 289-295.
30. Stricker-Krongrad A, Max JP, Musse N, Nicolas JP, Burlet C, Beck B. Increased threshold concentrations of neuropeptide Y for a stimulatory effect on food intake of obese Zucker rats changes in the microstructure of the feeding behavior. Brain Res 1994; 660: 162-166.
31. Merlo Pich E, Messori B, Zoli M, Ferraguti F, Marrama P, Biagini G, Fuxe K, Agnati LF. Feeding and drinking responses to neuropeptide Y injections in the paraventncular hypothalamic nucleus of aged rats. Brsin Res 1992; 575: 265-271.
32. Estes KS, Simpkins JW. Age-related alterations in catecholamine concentrations in discrete preoptic area and hypothalamic regions in the male rat. Brain Res 1980; 194: 556-560.
33. Reiss DJ, Ross RA, Joh TH. Changes in the activity and amounts of enzymes synthesizing catecholamines and acetylcholine in brain, adrenal medulla and synpathetic ganglia of aged rat and mouse. Brain Res 1977; 136: 465-474.
34. Roubein IF, Embree LJ, Jackson DN. Changes in catecholamine levels in discrete regions of rat brain during aging. Exp Aging Res 1986; 12: 193-196.
35. Venero JL, Machado A, Cano J. Turnover of dopamine and serotonin and their metabolites in the striatum of aged rats. J Neurochem 1991; 56: 1940-1948.
36. Arranz B, Blennow K, Ekman R, Eriksson A, Manson JE, Marcusson J. Brain monoaminergic and neuropeptidergic variations in human aging. J Neural Transm 1996; 103: 101-115.
37. Carfagna N, Trunzo F, Moretti A. Brain catecholamine turnover in aging rats. Exp Gerontol 1985; 20: 265-269.
38. Freeman GB, Gibson CE. Selective alteration of mouse brain neurotransmitter release with age. Neurobiol Aging 1987; 8: 147-152.
39. 3H-dopamine accumulation and release from striatal slices in young mature and senescent rats. Brain Res 1981; 16: 436-440.
40. Paxinos G, Watson C. The rat brain in stereotaxic coordinates. Academic Press: New York, 1986.
41. Nicolaïdis S, Rowland N, Meile MJ, Marfaing-Jallat P, Pesez A. A flexible technique for long-term infusions in unrestrained rats. Pharmacol Biochem Behav 1974; 2: 131-136.
42. Westerink BHC. Brain microdialysis and its application for the study of animal behavior. Behav Brain Res 1995; 70: 103-124.
43. Adell A, Carceller A, Artigas F. Regional distribution of extracellular 5-hydroxytryptamine and 5-hydroxyindolacetic acid in the brain of freely moving rats. J Neurochem 1991; 56: 709-712.
44. Wood PL, Altar CA. Dopamine release in vivo from nigrostriatal, mesolimbic and mesocortical neurons: utility of 3-methoxytyramine measurements. Pharmacol Rev 1988; 148: 327-334.
45. Stern JS, Johnson P. Spontaneous activity and adipose cellularity in genetically obese Zucker rats (fa-fa). Metabolism 1977; 26: 371-380.
46. Kubanis P, Zornetzer SF. Age-related behavioral and neurological changes: a review with an emphasis on memory. Behav Neural Biol 1981; 31: 115-172.
47. Roth RH, Walter JR, Aghajanian GK. Effect of impulse flow on the release and synthesis of dopamine in the rat striatum. In: Usdin E, Snyder SH (eds). Frontiers in Catecholamine Research. Pergamon Press: New York, 1973, pp 567-574.
48. Westerink BHC. Sequence and significance of dopamine metabolism in the rat brain. Neurochem Int 1985; 7: 221-227
49. Cerrito F, Aloisi G, Arminio P. Age-related changes in rat brain monoamines release: peculiarity of dopamine release. J Neurosci Res 1993; 34: 364-370.
50. Hastings JA, Pavia JM, Morris MJ. Altered in vivo catecholamine release in the hypothalamic paraventricular nucleus of the aged rat. Naunyn-Schmied Arch Pharmacol 1996; 353: 161-167.
51. Fairbrother IS, Arbuthnott GW, Kelly JS, Butcher SP. In vivo mechanisms underlying dopamine release from rat nigrostriatal terminals: studies using potassium and tyramine. J Neurochem 1990; 54: 1844-1851.
52. Nakano M, Mizuno T. Age-related changes in the metabolism of neurotransmitters in rat striatum: a microdialysis study. Mech Ageing Dev 1996; 86: 95-104.
53. Demarest KT, Riegle GD, Moore KE. Characteristics of dopaminergic neurons in the aged male rat. Neuroendocrinology 1980; 31: 222-227.
54. Pradhan SN. Minireview: central neurotransmitters and aging. Life Sci 1980; 26: 1643-1646.