MODIFICATION OF PATHOLOGIC CHANGES IN TOXICOLOGICAL STUDIES DUE TO ENDOTOXIN DERIVED FROM INTESTINAL FLORA I. Microscopic Findings in Various Organs and Tissues from Endotoxin-Treated Rats

In order to clarify the characteristics of the toxic effects of endotoxins on various organs and tissues, single and multiple doses studies of commercial endotoxins were carried out using Fischer and SD rats for the purpose of microscopic examination. In the single dose study using a dose of 10 mg/k...

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Published inJournal of Toxicologic Pathology Vol. 6; no. 1; pp. 89 - 104
Main Authors Fujii-Murakami, Hisako, Inomata, Norikazu, Shimoji, Naoshi, Noguchi, Osamu, Takagi, Hidetoshi, Ogasawara, Hiroyuki, Murata, Akiko, Harada, Yasushi
Format Journal Article
LanguageEnglish
Published JAPANESE SOCIETY OF TOXICOLOGIC PATHOLOGY 1993
The Japanese Society of Toxicologic Pathology
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ISSN0914-9198
1881-915X
DOI10.1293/tox.6.89

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Abstract In order to clarify the characteristics of the toxic effects of endotoxins on various organs and tissues, single and multiple doses studies of commercial endotoxins were carried out using Fischer and SD rats for the purpose of microscopic examination. In the single dose study using a dose of 10 mg/kg of endotoxin Salmonella typhimurium, changes of the lungs, liver, gastrointestinal tract, and thymus were observed primarily in a tme-dependent manner. After onset of hemorrhagic changes of some organs and tissues at the early stage after dosing, hepatic changes such as activation of Kupffer cells, formation of thrombi and necrosis of hepatocytes, activation of alveolar macrophages and polymorphonuclear cell infiltration in the lungs, and lymphoid depletion of the thymus were observed from 2 or 4 hours after dosing. On the other hand, in the multiple doses study using doses from 0.1 to 1.0mg/kg/day of the same endotoxin, activation of Kupffer cells in the liver and activation of alveolar macrophages in the lungs, and lymphoid depletion of the thymus were observed primarily. We concluded that the endotoxin-modified changes should be taken into consideration when we interprete and judge the results of a general toxicity study of an agent, which has effects related to generation of endotoxins from intestinal flora. Moreover, it is also necessary to understand the different sensitivity to endotoxin among the animal strain for this situation, because the microscopic changes in SD rats due to endotoxin were more prominent to be compared with those in Fischer rats in a single dose study.
AbstractList In order to clarify the characteristics of the toxic effects of endotoxins on various organs and tissues, single and multiple doses studies of commercial endotoxins were carried out using Fischer and SD rats for the purpose of microscopic examination. In the single dose study using a dose of 10 mg/kg of endotoxin Salmonella typhimurium, changes of the lungs, liver, gastrointestinal tract, and thymus were observed primarily in a tme-dependent manner. After onset of hemorrhagic changes of some organs and tissues at the early stage after dosing, hepatic changes such as activation of Kupffer cells, formation of thrombi and necrosis of hepatocytes, activation of alveolar macrophages and polymorphonuclear cell infiltration in the lungs, and lymphoid depletion of the thymus were observed from 2 or 4 hours after dosing. On the other hand, in the multiple doses study using doses from 0.1 to 1.0mg/kg/day of the same endotoxin, activation of Kupffer cells in the liver and activation of alveolar macrophages in the lungs, and lymphoid depletion of the thymus were observed primarily. We concluded that the endotoxin-modified changes should be taken into consideration when we interprete and judge the results of a general toxicity study of an agent, which has effects related to generation of endotoxins from intestinal flora. Moreover, it is also necessary to understand the different sensitivity to endotoxin among the animal strain for this situation, because the microscopic changes in SD rats due to endotoxin were more prominent to be compared with those in Fischer rats in a single dose study.
In order to clarify the characteristics of the toxic effects of endotoxins on various organs and tissues, single and multiple doses studies of commercial endotoxins were carried out using Fischer and SD rats for the purpose of microscopic examination. In the single dose study using a dose of 10mg/kg of endotoxin Salmonella typhimurium, changes of the lungs, liver, gastrointestinal tract, and thymus were observed primarily in a tme-dependent manner. After onset of hemorrhagic changes of some organs and tissues at the early stage after dosing, hepatic changes such as activation of Kupffer cells, formation of thrombi and necrosis of hepatocytes, activation of alveolar macrophages and polymorphonuclear cell infiltration in the lungs, and lymphoid depletion of the thymus were observed from 2 or 4 hours after dosing. On the other hand, in the multiple doses study using doses from 0.1 to 1.0 mg/kg/day of the same endotoxin, activation of Kupffer cells in the liver and activation of alveolar macrophages in the lungs, and lymphoid depletion of the thymus were observed primarily. We concluded that the endotoxin-modified changes should be taken into consideration when we interprete and judge the results of a general toxicity study of an agent, which has effects related to generation of endotoxins from intestinal flora. Moreover, it is also necessary to understand the different sensitivity to endotoxin among the animal strain for this situation, because the microscopic changes in SD rats due to endotoxin were more prominent to be compared with those in Fischer rats in a single dose study.
Author Ogasawara, Hiroyuki
Noguchi, Osamu
Takagi, Hidetoshi
Inomata, Norikazu
Shimoji, Naoshi
Fujii-Murakami, Hisako
Murata, Akiko
Harada, Yasushi
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References 5. Liehr, H, Englisch, G, and Rasenack, U: Lactulosea drug with antiendotoxin effect. Hepato-Gasteroenterology 27: 356-360, 1980.
12. Mckey, DG, Margaretten, W, and Csavossy, 1: An electron microscopic study of the effects of bacterial endotoxin on the blood-vascilar system. Lab Invest 15: 1815-1829, 1966.
9. Ravin, HA, Rowley, D, Jenkins, C, and Fine, J: On the absorption of bacterial endotoxin from the gastro-intestinal tract of the normal and shocked animal. J Exp Med 112: 783-792, 1960.
1. Olofsson, P, Nylander, G, and Olsson, P: Endotoxin-transport routes and kinetics in intestinal ischemia. Acta Chir Scand 151: 635-639, 1985.
4. Goldman, P: Biochemical pharmacology of the intestinal flora. Ann Rev Pharmacol Toxicol 18: 523-539, 1978.
11. Hirama, T and Ogawa, K.: An electron microscopic study of the rat liver following endotoxin administration. Sapporo Igaku-zasshi 46: 425-447, 1977.
22. Garcia, R, Viloria, MD, and Municio, AM: Influence of E. coli endotoxin on ACTH induced adrenal cell steroidgenesis. J Steroid Biochem 22: 377-385, 1985.
16. Tsujimoto, M, Yokota, S, Vil ek, J, and Weissmann, G: Tumor necrosis factor provokes superoxide anion generation from neutrophils. Biochem Biophys Res Commun 137: 1094-1100, 1986.
24. Yoshitake, H and Hirata, K: studies on the pathogenesis of early hepatic changes after endotoxin treatment in the rat. (1) Changes in hepatic parenchymal cells and non-parenchymal cells isolated periodically after endotoxin treatment. Sapporo Igaku-zasshi 57: 237-248, 1988.
27. Helander, I, Saxen, H, Salkinoja-Salonen, M, and Rylander, R: Pulmonary toxicity of endotoxins: comparison of lipopolyssacharides from various bacterial species. Infect Immun 35: 528-532, 1982.
31. Remick, DG, Strieter, RM, Eskandari MK, Nguyen, DT, Genord, MA, Raiford, CL and Kunkel, SL: Role of tumor necrosis factor-α in lipopolyssacharide-induced pathologic alteration. Am J Pathol 136: 49-60, 1990.
26. Snella, M-C and Rylander, R: Lung cell reactions after inhalation of bacterial lypopolyssacharides. Eur J Res Dis 63: 550-557, 1982.
29. Bosch, MA, Garcia, R, Pagani, R, Portoles, MT, Diaz-Laviada I, Abarca, S, Aninaga, MJ, Risco, C, and Municio, AM: Induction of reversible shock by Escherichia coli lypopolyssacharide in rats. Changes in serum and cell membrane parameter. Br J Exp Pathol 69: 805-812, 1988.
18. Nagano, T, Kita, T, and Tanaka, N: The immunocytochemical localization of tumor necrosis factor and leukotriene in the rat liver after treatment with lypopolyssacharide. Int J Exp Pathol 73: 675-683, 1992.
15. Pohlman, TH, Stanness, KA, Beatty, PG, Ochs, HD, and Harlan, JH: An endothelial cell surface factor (s) induced in vitro by lypopolyssacharide, interleukine 1, and tumor necrosis factor-α. Increases neutrophil adherence by a CDw 18-dependent mechanism. J Immumol 136: 4548-4553, 1986.
17. Wallace, JL and Whittle, BJR: Gastrointestinal damage induced by platelet-activating factor. Digest Dis Sci 33: 225-232, 1988.
30. Mobery, GP: Site of action of endotoxins on hypothalmic-pituitary-adrenal axis Am J Physiol 220: 397-400, 1971.
19. Chen, AR, Mckinnon, KP, and Koren, HS: Lipopolyssacharide (LPS) stimulates fresh human monocytes to lyse actinomycin D-treated WEH1-164 target cells via increased secretion of a monokine similar to tumor necrosis factor. J Immunol 135: 3978-3987, 1985.
2. Berg, RD: Bacterial translocation from intestine. Exp Anim 34: 1-16, 1985.
3. Shibayama, Y: Endotoxin and liver injury. Metab Dis 26: 441-451, 1989.
13. Flohé, L and Giertz, H: Endotoxin, arachidonic acid, and superoxide formation Rev Infect Dis 9 (Suppl. 5): 5553-5561, 1987.
25. Chensue, SW, Terebuh, PD, Remik, DG, Scales, WE, and Kunkel, SL: In Vitro biologic and immunohistochemical analysis of interleukin-1 alpha, beta and tumor necrosis factor during experimental endoxemia. Kinetics, Kupffer cell experession, and glucocorticoid effects. Am J Pathol 138: 395-402, 1991.
8. Nagura, H and Watanabe, K: Intestinal local immune system. Saishin-Igaku 38: 2440-2449, 1983.
10. Shute, K: Effect of intraluminal oxygen on endotoxin absorption in experimental occulusion of the superior mesenteric artery. Gut 18: 567-570, 1977.
20. Kornbluth, RS and Edgington, TS: Tumor necrosis factor production by human monocyte is a regulated event: Induction of TNF-α-mediated cellular cytotoxicity by endotoxin. J Immunol 137: 2585-2591, 1986.
14. Smedegård, G, Cui, L, and Hugh, TE: Endotoxininduced shock in the rat. A role for C5a. Am J Pathol 135: 489-497, 1989.
28. Hsueh, W, Gonzalez-Crussi, F, and Arroyave, JL: Platelet-activating factor-induced ischemic bowel necrosis. An investigation of secondary mediators in its pathogenesis. Am J Pathol 122: 231-239, 1986.
21. Fujiwara, H and Kuratsuka, K: Enhancement by lead acetate of body weight-decreasing activity of endotoxin: Quantitative comparison of some administration methods of lead acetate. Jpn J Med Sci Biol 33: 203-216, 1980.
23. Ogawa, Y, Kiso, M, and Hasegawa, A: Biological activities of lipid A analogs. Metab Dis 26: 415-427, 1989.
33. Tiegs, G and Wendel, A: Leukoriene-mediated liver injury. Biochem Pharmacol 37: 2569-2573, 1988.
6. Sherman, P, Fleming, N, Forstner, J, Roomi, N, and Forstner, G: Bacteria and the mucus blanket in experimental small bowel bacteria overgrowth. Am J Pathol 126: 527-534, 1987.
7. Brown, WR, Isobe, Y, and Nakane, PK: Studies on translocation of immunoglobulins across intestinal epithelium. II. Immunoelectron-microscopic localization of immunoglobulins and secretory component in human intestinal mucosa. Gasteroenterology 71: 985-995, 1976.
32. Keane, WF, Gekker, G, Schlievert, PM, and Peterson, PK: Enhancement of endotoxin-induced isolated renal tubular cell injury by toxic shock syndrome toxin 1. Am J Pathol 122: 169-176, 1986.
References_xml – reference: 17. Wallace, JL and Whittle, BJR: Gastrointestinal damage induced by platelet-activating factor. Digest Dis Sci 33: 225-232, 1988.
– reference: 5. Liehr, H, Englisch, G, and Rasenack, U: Lactulosea drug with antiendotoxin effect. Hepato-Gasteroenterology 27: 356-360, 1980.
– reference: 6. Sherman, P, Fleming, N, Forstner, J, Roomi, N, and Forstner, G: Bacteria and the mucus blanket in experimental small bowel bacteria overgrowth. Am J Pathol 126: 527-534, 1987.
– reference: 18. Nagano, T, Kita, T, and Tanaka, N: The immunocytochemical localization of tumor necrosis factor and leukotriene in the rat liver after treatment with lypopolyssacharide. Int J Exp Pathol 73: 675-683, 1992.
– reference: 9. Ravin, HA, Rowley, D, Jenkins, C, and Fine, J: On the absorption of bacterial endotoxin from the gastro-intestinal tract of the normal and shocked animal. J Exp Med 112: 783-792, 1960.
– reference: 15. Pohlman, TH, Stanness, KA, Beatty, PG, Ochs, HD, and Harlan, JH: An endothelial cell surface factor (s) induced in vitro by lypopolyssacharide, interleukine 1, and tumor necrosis factor-α. Increases neutrophil adherence by a CDw 18-dependent mechanism. J Immumol 136: 4548-4553, 1986.
– reference: 19. Chen, AR, Mckinnon, KP, and Koren, HS: Lipopolyssacharide (LPS) stimulates fresh human monocytes to lyse actinomycin D-treated WEH1-164 target cells via increased secretion of a monokine similar to tumor necrosis factor. J Immunol 135: 3978-3987, 1985.
– reference: 25. Chensue, SW, Terebuh, PD, Remik, DG, Scales, WE, and Kunkel, SL: In Vitro biologic and immunohistochemical analysis of interleukin-1 alpha, beta and tumor necrosis factor during experimental endoxemia. Kinetics, Kupffer cell experession, and glucocorticoid effects. Am J Pathol 138: 395-402, 1991.
– reference: 16. Tsujimoto, M, Yokota, S, Vil ek, J, and Weissmann, G: Tumor necrosis factor provokes superoxide anion generation from neutrophils. Biochem Biophys Res Commun 137: 1094-1100, 1986.
– reference: 8. Nagura, H and Watanabe, K: Intestinal local immune system. Saishin-Igaku 38: 2440-2449, 1983.
– reference: 33. Tiegs, G and Wendel, A: Leukoriene-mediated liver injury. Biochem Pharmacol 37: 2569-2573, 1988.
– reference: 2. Berg, RD: Bacterial translocation from intestine. Exp Anim 34: 1-16, 1985.
– reference: 20. Kornbluth, RS and Edgington, TS: Tumor necrosis factor production by human monocyte is a regulated event: Induction of TNF-α-mediated cellular cytotoxicity by endotoxin. J Immunol 137: 2585-2591, 1986.
– reference: 12. Mckey, DG, Margaretten, W, and Csavossy, 1: An electron microscopic study of the effects of bacterial endotoxin on the blood-vascilar system. Lab Invest 15: 1815-1829, 1966.
– reference: 4. Goldman, P: Biochemical pharmacology of the intestinal flora. Ann Rev Pharmacol Toxicol 18: 523-539, 1978.
– reference: 28. Hsueh, W, Gonzalez-Crussi, F, and Arroyave, JL: Platelet-activating factor-induced ischemic bowel necrosis. An investigation of secondary mediators in its pathogenesis. Am J Pathol 122: 231-239, 1986.
– reference: 3. Shibayama, Y: Endotoxin and liver injury. Metab Dis 26: 441-451, 1989.
– reference: 11. Hirama, T and Ogawa, K.: An electron microscopic study of the rat liver following endotoxin administration. Sapporo Igaku-zasshi 46: 425-447, 1977.
– reference: 21. Fujiwara, H and Kuratsuka, K: Enhancement by lead acetate of body weight-decreasing activity of endotoxin: Quantitative comparison of some administration methods of lead acetate. Jpn J Med Sci Biol 33: 203-216, 1980.
– reference: 27. Helander, I, Saxen, H, Salkinoja-Salonen, M, and Rylander, R: Pulmonary toxicity of endotoxins: comparison of lipopolyssacharides from various bacterial species. Infect Immun 35: 528-532, 1982.
– reference: 23. Ogawa, Y, Kiso, M, and Hasegawa, A: Biological activities of lipid A analogs. Metab Dis 26: 415-427, 1989.
– reference: 29. Bosch, MA, Garcia, R, Pagani, R, Portoles, MT, Diaz-Laviada I, Abarca, S, Aninaga, MJ, Risco, C, and Municio, AM: Induction of reversible shock by Escherichia coli lypopolyssacharide in rats. Changes in serum and cell membrane parameter. Br J Exp Pathol 69: 805-812, 1988.
– reference: 10. Shute, K: Effect of intraluminal oxygen on endotoxin absorption in experimental occulusion of the superior mesenteric artery. Gut 18: 567-570, 1977.
– reference: 31. Remick, DG, Strieter, RM, Eskandari MK, Nguyen, DT, Genord, MA, Raiford, CL and Kunkel, SL: Role of tumor necrosis factor-α in lipopolyssacharide-induced pathologic alteration. Am J Pathol 136: 49-60, 1990.
– reference: 7. Brown, WR, Isobe, Y, and Nakane, PK: Studies on translocation of immunoglobulins across intestinal epithelium. II. Immunoelectron-microscopic localization of immunoglobulins and secretory component in human intestinal mucosa. Gasteroenterology 71: 985-995, 1976.
– reference: 14. Smedegård, G, Cui, L, and Hugh, TE: Endotoxininduced shock in the rat. A role for C5a. Am J Pathol 135: 489-497, 1989.
– reference: 26. Snella, M-C and Rylander, R: Lung cell reactions after inhalation of bacterial lypopolyssacharides. Eur J Res Dis 63: 550-557, 1982.
– reference: 24. Yoshitake, H and Hirata, K: studies on the pathogenesis of early hepatic changes after endotoxin treatment in the rat. (1) Changes in hepatic parenchymal cells and non-parenchymal cells isolated periodically after endotoxin treatment. Sapporo Igaku-zasshi 57: 237-248, 1988.
– reference: 32. Keane, WF, Gekker, G, Schlievert, PM, and Peterson, PK: Enhancement of endotoxin-induced isolated renal tubular cell injury by toxic shock syndrome toxin 1. Am J Pathol 122: 169-176, 1986.
– reference: 13. Flohé, L and Giertz, H: Endotoxin, arachidonic acid, and superoxide formation Rev Infect Dis 9 (Suppl. 5): 5553-5561, 1987.
– reference: 22. Garcia, R, Viloria, MD, and Municio, AM: Influence of E. coli endotoxin on ACTH induced adrenal cell steroidgenesis. J Steroid Biochem 22: 377-385, 1985.
– reference: 1. Olofsson, P, Nylander, G, and Olsson, P: Endotoxin-transport routes and kinetics in intestinal ischemia. Acta Chir Scand 151: 635-639, 1985.
– reference: 30. Mobery, GP: Site of action of endotoxins on hypothalmic-pituitary-adrenal axis Am J Physiol 220: 397-400, 1971.
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Subtitle I. Microscopic Findings in Various Organs and Tissues from Endotoxin-Treated Rats
Title MODIFICATION OF PATHOLOGIC CHANGES IN TOXICOLOGICAL STUDIES DUE TO ENDOTOXIN DERIVED FROM INTESTINAL FLORA
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