%0 Journal Article %1 Scheding.1992b %A Scheding, S. %A Loeffler, Markus %A Schmitz, S. %A Seidel, H. J. %A Wichmann, Heinz-Erich %D 1992 %J Toxicology %K IMISE-Publikationen %N 3 %P 265–279 %T Hematotoxic effects of benzene analyzed by mathematical modeling %V 72 %X The hematopoietic cell response to benzene intoxication in mice (during and after long-term inhalation) was analyzed by a mathematical model of murine hematopoiesis. Two complementary methods, Time-Curve and Steady-State Analysis, were developed to identify target cells for benzene toxicity and to quantify the extent of damage in different stages of development of these target cells. We found that (i) erythropoietic cells were the most sensitive; (ii) granulopoietic cells were about half as sensitive as erythropoietic and (iii) hematopoietic stem cells exhibited a sensitivity that ranged between that of erythropoietic and granulopoietic cells. A dose-response relationship between benzene levels and damage in target cells (valid from 1 to more than 900 ppm) was derived that was linear for doses up to 300 ppm and plateaued thereafter. This relationship indicated that benzene-induced hematotoxicity is subject to a saturable process. Recovery of hematopoiesis following chronic benzene intoxication was simulated for different doses and preceding exposure periods. The impaired recovery following exposure periods greater than 8 weeks could be explained by a severe reduction in the maximum self-maintenance of stem cells. This study indicates that the present mathematical model represents a useful approach to investigate alternate hypotheses for the action of hematotoxic agents.

@article{Scheding.1992b, abstract = {The hematopoietic cell response to benzene intoxication in mice (during and after long-term inhalation) was analyzed by a mathematical model of murine hematopoiesis. Two complementary methods, Time-Curve and Steady-State Analysis, were developed to identify target cells for benzene toxicity and to quantify the extent of damage in different stages of development of these target cells. We found that (i) erythropoietic cells were the most sensitive; (ii) granulopoietic cells were about half as sensitive as erythropoietic and (iii) hematopoietic stem cells exhibited a sensitivity that ranged between that of erythropoietic and granulopoietic cells. A dose-response relationship between benzene levels and damage in target cells (valid from 1 to more than 900 ppm) was derived that was linear for doses up to 300 ppm and plateaued thereafter. This relationship indicated that benzene-induced hematotoxicity is subject to a saturable process. Recovery of hematopoiesis following chronic benzene intoxication was simulated for different doses and preceding exposure periods. The impaired recovery following exposure periods greater than 8 weeks could be explained by a severe reduction in the maximum self-maintenance of stem cells. This study indicates that the present mathematical model represents a useful approach to investigate alternate hypotheses for the action of hematotoxic agents.}, added-at = {2014-10-17T12:55:47.000+0200}, author = {Scheding, S. and Loeffler, Markus and Schmitz, S. and Seidel, H. J. and Wichmann, Heinz-Erich}, biburl = {https://www.bibsonomy.org/bibtex/2b01197c9e0de025f879d509d82da99db/drtester}, interhash = {c128a0e4d750ac2b8aa38167f49860fc}, intrahash = {b01197c9e0de025f879d509d82da99db}, journal = {Toxicology}, keywords = {IMISE-Publikationen}, number = 3, pages = {265–279}, timestamp = {2014-12-03T00:00:15.000+0100}, title = {Hematotoxic effects of benzene analyzed by mathematical modeling}, volume = 72, year = 1992 }