The influence of septal lesions on sodium and water retention induced by Walker 256 tumor

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Brazilian Journal of Medical and Biological Septal lesions and tumor-induced Na + Research (1999) 32: 39-317 retention ISSN 1-879X 39 The influence of septal lesions on sodium and water retention induced by Walker 256 tumor F. Guimarães 1, O. Rettori 2, A.N. Vieira-Matos 2 and G.A. Fernandes 3 1 Departamento de Fisiologia Animal e Biofísica, Instituto de Biologia, 2 Laboratório de Pesquisas Bioquímicas, Centro de Atenção Integral à Saúde da Mulher, and 3 Núcleo de Medicina e Cirurgia Experimental, Faculdade de Ciências Médicas, Universidade Estadual de Campinas, Campinas, SP, Brasil Correspondence F. Guimarães Laboratório de Pesquisas Bioquímicas CAISM, UNICAMP Caixa Postal 6151 1381-97 Campinas, SP Brasil Fax: +55-19-231-5273 Publication supported by FAPESP. Received October 28, 1997 Accepted November 17, 1998 Abstract Key words Na + retention Secondary diuretic response Tumor systemic effects Septal area lesion Multifocal tumor inoculation Walker 256 tumor

31 F. Guimarães et al. Introduction Material and Methods Animals and brain surgery Experimental conditions and parameters measured

Septal lesions and tumor-induced Na + retention 311 Tumor The multifocal tumor model Data synchronization Data analysis Experimental design

312 F. Guimarães et al. Figure 1 - Septal-lesioned rats. Top, Toluidine blue-stained coronal section (2-3 µm) and bottom, schematic representation of brain planes showing the extent of the lesion, which involved the medial and lateral (dorsal, intermediate and ventral) septal nucleus, besides part of the septofimbrial nucleus. In some rats, the lesion may have included the septohypothalamic nucleus, triangular septal nucleus, septal projection of the fornix and a small anterior portion of the corpus callosum. Results Brain lesion 1. mm.48 mm.2 mm Tumor and disease evolution -.26 mm Table 1 - Average duration (days) of the subclinical () and clinical () periods and survival (SV) of rats multifocally inoculated with Walker 256 tumor, sham-operated (SW; N = 7) and septal-lesioned (LW; N = 15). The values are reported as the means ± SEM for the number of rats indicated by N. SW (N = 7) LW (N = 15) 3. ±.2 2.6 ±.1 7.7 ±.6 7. ±.3 SV 1.7 ±.6 9.6 ± 2.5

Septal lesions and tumor-induced Na + retention 313 Body weight (%) 11 15 1 95 9 85 25 2 SW SFR LW LFR Fractional sodium balance Food intake (g) Renal Na + excretion (mmol/day) 15 1 5 4 3 2 1-2 2 4 6 8 1 12 Days after tumor inoculation Figure 2 - Time course of the changes in body weight and renal Na + excretion in septal-lesioned tumor-bearing rats (LW; N = 15) compared with shamoperated tumor-bearing rats (SW; N = 7) and their respective non-tumorbearing controls, sham-operated food-restricted (SFR; N = 7) and lesioned food-restricted (LFR; N = 1) rats. Food intake is given for the SFR and LFR groups. During the clinical period (), body weight gain and renal Na + excretion in LW rats were temporarily altered in relation to the SW rats (LSD test, P<.5 for SW x LW)., Subclinical period.

314 F. Guimarães et al. Table 2 - Body weight (%) from the fourth to the seventh day after tumor cell inoculation in sham-operated tumor-bearing (SW; N = 7) and septal-lesioned tumor-bearing (LW; N = 15) rats. Data are compared to their respective non-tumor-bearing controls, i.e., shamoperated food-restricted (SFR; N = 7) and septal-lesioned food-restricted (LFR; N = 1) rats. abc P<.5 (least significant difference test, SW x SFR and LW x LFR). Day Body weight (%) SW (N = 7) SFR (N = 7) LW (N = 15) LFR (N = 1) 4 11.8 ±.6 1.5 ±.4 99.8 ±.5 1.5 ±.4 5 12.2 ± 1. a 98.7 ±.3 a 1.2 ±.9 99.2 ±.2 6 14. ± 1. ac 97.1 ±.3 a 11.9 ±.7 bc 98.1 ±.3 b 7 15.3 ± 1.1 ac 95.3 ±.3 a 12.7 ± 1.1 bc 97.4 ±.3 b Table 3 - Renal sodium excretion (mmol/day) from the fourth to the seventh day after tumor cell inoculation in sham-operated tumor-bearing (SW; N = 7) and septal-lesioned tumor-bearing (LW; N = 15) rats. Data are compared to their respective non-tumor-bearing controls, i.e., shamoperated food-restricted (SFR; N = 7) and septal-lesioned food-restricted (LFR; N = 1) rats. abc P<.5 (least significant difference test, SW x SFR and LW x LFR). Day Renal Na + excretion (mmol/day) SW (N = 7) SFR (N = 7) LW (N = 15) LFR (N = 1) 4 1.4 ±.2 ab 2.8 ±.2 a 2.6 ±.2 b 2.1 ±.1 5 1.1 ±.1 ab 2.8 ±.2 ac 1.9 ±.1 b 2.3 ±.1 c 6 1.3 ±.2 ab 2.5 ±.2 a 1.8 ±.1 b 2.2 ±.1 7 1.3 ±.2 a 2.2 ±.1 a 1.4 ±.1 b 2.1 ±.1 b Changes in body fluids Osmolar excretion

Septal lesions and tumor-induced Na + retention 315 Autopsy findings Discussion Tumor and disease evolution Effect of septal lesions on tumor-induced alterations in water and electrolyte balances Fractional Na + balance (%) 8 6 4 2-2 -4 SW SFR LW LFR -6-2 2 4 6 8 1 12 Days after tumor inoculation Figure 3 - Time course of sodium retention induced by the tumor in septal-lesioned tumor-bearing rats (LW; N = 15) compared with sham-operated tumor-bearing rats (SW; N = 7) and their respective non-tumor-bearing controls, sham-operated foodrestricted (SFR; N = 7) and lesioned food-restricted (LFR; N = 1) rats. The fractional sodium balance was calculated as (input-output) x 1/input, where input is the food intake (g/day) x diet sodium content (meq/g), and output is the urine volume (ml/day) x urine sodium concentration (meq/ml). During the clinical period (), the tumorinduced Na + retention was temporarily reduced in LW rats compared with SW rats (least significant difference test, P<.5 for SW x LW)., Subclinical period. Urine volume changes (ml/1 g body weight) 6 4 2 SW SFR LW LFR -2-2 2 4 6 8 1 12 Days after tumor inoculation Figure 4 - Time course of urine output observed in septal-lesioned tumor-bearing rats (LW; N = 15), compared with sham-operated tumor-bearing (SW; N = 7) and their respective non-tumor-bearing controls, sham-operated food-restricted (SFR; N = 7) and lesioned food-restricted (LFR; N = 1) rats. During the clinical period (), the urine production was significantly increased in LW (least significant difference test, P<.5 for SW x LW)., Subclinical period.

316 F. Guimarães et al. Figure 5 - Fluid retention changes of sham-operated (SW) and septal-lesioned (LW) tumorbearing groups shown by plotting the differences between body weight of tumor-bearing groups and their respective controls (Figure 2; SW minus shamoperated food-restricted (SFR) and LW minus septal-lesioned food-restricted (LFR))., Subclinical period;, clinical period. Possible mechanism of temporary reduction in sodium reabsorption in LW rats 2 15 1 5-5 Body weight changes (%)25 SW - SFR LW - LFR -2 2 4 6 8 1 12 Days after tumor inoculation Table 4 - Comparison of osmolar excretion (mosm/day) during the clinical period (; average of values obtained on days 5 to 7) and the subclinical period () in septal-lesioned tumorbearing (LW; N = 15), sham-operated tumor-bearing (SW; N = 7), sham-operated food-restricted (SFR; N = 7) and septal-lesioned food-restricted (LFR; N = 1) groups. (mosm/day) SW (N = 7) 35.2 ± 2.1 33.3 ± 2.9 SFR (N = 7) 35.4 ± 2.8 36.3 ± 2.3 LW (N = 15) 45.3 ± 2.1 41.3 ± 1.6 LFR (N = 1) 32.6 ± 2.1 31.1 ± 1.7 Conclusion

Septal lesions and tumor-induced Na + retention 317 Acknowledgments References 1. Eastern Cooperative Oncology Group (198). Prognostic effect of weight loss prior to chemotherapy in cancer patients. American Journal of Medicine, 69: 491-497. 2. Graf W, Glimelius B, Pahlman L & Bergström R (1991). Determinants of prognosis in advanced colorectal cancer. European Journal of Cancer, 77: 1119-1123. 3. Pasqualetti P, Casale R, Collacciani A & Colantonio D (1991). Prognostic factors in multiple myeloma: a new staging system based on clinical and morphological features. European Journal of Cancer, 27: 1123-1126. 4. Rustig VK (1987). Epidemiology of hepatocellular carcinoma. Gastroenterology Clinics of North America, 16: 545-551. 5. Tacaks FJ (1974). Fluid and electrolyte problems in patients with advanced carcinoma. Medical Clinics of North America, 59: 449-457. 6. Blackburn SL, Maini BS, Bistrian BR & McDermott WV (1977). The effect of cancer on nitrogen, electrolyte, and mineral metabolism. Cancer Research, 37: 2348-2353. 7. Garattini S, Bizzi A, Conelli MG, Guaitani A, Samanin R & Spreafico F (198). Anorexia and cancer in animals and man. Cancer Treatment Reviews, 7: 115-14. 8. Baillie P, Millar FK & Pratt AW (1965). Food intake and Walker tumor growth in rats with hypothalamic lesions. American Journal of Physiology, 21: 293-3. 9. Scott OCA (1991). Tumor transplantation and tumor immunity: A personal view. Cancer Research, 51: 757-763. 1. Rettori O, Vieira-Matos AN & Tahin QS (1995). Variability and discontinuity of the pathognomic systemic effects caused by the Walker-256 tumor progression in rats. Tumori, 81: 37-377. 11. Rettori O, Vieira-Matos AN & Gontijo JAR (1996). Reduced renal sodium excretion in Walker-256 tumor-bearing rats. Acta Physiologica Latino Americana, 46: 111-118. 12. Morrison SD (1968). Effect of growth of a tumor on the regulation of water intake. Journal of the National Cancer Institute, 41: 1241-1248. 13. Morrison SD (1971). Water intake and exchange and hydration of rats during growth of Walker 256 carcinoma. Journal of the National Cancer Institute, 46: 825-83. 14. Morrison SD (1974). Sodium and the cachexia and hypophagia of tumor growth. Journal of the National Cancer Institute, 52: 869-874. 15. Toal JN, Millar FK, Brooks RH & White V (196). Sodium retention by rats bearing the Walker carcinosarcoma 256. American Journal of Physiology, 2: 175-181. 16. Harvey JA & Hunt HF (1965). Effect of septal lesions on thirst in the rat as indicated by water consumption and operant responding for water reward. Journal of Comparative and Physiological Psychology, 59: 49-56. 17. Negro Vilar A, Gentil CG & Antunes- Rodrigues J (1965). Influência do sistema límbico na ingestão de cloreto de sódio e água no rato. Ciência e Cultura, 17: 253 (Abstract). 18. Covian MR (1966). Fisiologia del área septal. Acta Physiologica Latino Americana, 16: 119-152. 19. Paxinos G & Watson C (1986). The Rat Brain in Stereotaxic Coordinates. 2nd edn. Academic Press, New York. 2. Paplowsky A & Isaacson RL (199). Nimodipine accelarates recovery from the hyper-emotionality produced by septal lesions. Behavioral and Neural Biology, 53: 133-139. 21. Pitts RF (1968). Regulation of volume and osmolar concentration of extracellular fluid. In: Pitts RF (Editor), Physiology of the Kidney and Body Fluids. Year Book Medical Publishers Incorporated, Chicago. 22. Haibara AS, Saad WA, Camargo LAA, Menani JV, Renzi A, De Luca Jr LA & Antunes-Rodrigues J (1992). Opiate activation suppresses the drinking pressor and natriuretic responses induced by cholinergic stimulation of the medial septal area. Brain Research Bulletin, 28: 155-16. 23. Bridge JG (1976). Unit activity in the septal nuclei during water deprivation, drinking, and rehydration. In: De France JF (Editor), Advances in Behavioral Biology. The Septal Nuclei. Plenum Press, New York.