Immunocytochemical studies on the distribution pattern of daunomycin in rat gastrointestinal tract
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Immunocytochemical studies on the distribution pattern of daunomycin in rat gastrointestinal tract. / Ohara, Koji; Shin, Masashi; Nakamuta, Hiromichi; Larsson, Lars-Inge; Hougaard, David M.; Fujiwara, Kuino.
In: Histochemistry and Cell Biology, Vol. 128, No. 3, 2007, p. 285-290.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Immunocytochemical studies on the distribution pattern of daunomycin in rat gastrointestinal tract
AU - Ohara, Koji
AU - Shin, Masashi
AU - Nakamuta, Hiromichi
AU - Larsson, Lars-Inge
AU - Hougaard, David M.
AU - Fujiwara, Kuino
PY - 2007
Y1 - 2007
N2 - The cancer drug daunomycin is used in treatment of leukemia but possesses severe side effects that involve the gastrointestinal tract. We therefore used a newly developed immunocytochemical procedure to determine the distribution of DM in the gastrointestinal tracts of rats after i.v. injection. Two hours after injection, DM was diffusely distributed in nuclei and most parts of the cytoplasm of intestinal epithelial cells. The cytoplasmic immunoreactivity for DM was most pronounced in small granules of the apical cytoplasm. Sixteen hours after injection, DM immunostaining was by and large absent in the villous epithelium but persisted in the intestinal crypts. In addition, staining was also detected in endothelial cells, scattered cells of the lamina propria and in smooth muscle cells. After 5 days, only little staining for DM remained. Similar findings were made in the colon. In the gastric mucosa, DM accumulation persisted at 16 h in some glandular cells but was lost from the surface epithelium. No staining was detected in saline-injected control rats. The distribution of DM accumulation correlated partially with the distribution of apoptotic cells as detected by the TUNEL procedure. Our results pinpoint that DM may exert prolonged effects on glandular and regenerative cells of the gastrointestinal tract - an observation that may explain the gastrointestinal toxicity of the drug. It seems possible that DM accumulation in surface epithelial cells is rapidly cleared through drug transporters.
AB - The cancer drug daunomycin is used in treatment of leukemia but possesses severe side effects that involve the gastrointestinal tract. We therefore used a newly developed immunocytochemical procedure to determine the distribution of DM in the gastrointestinal tracts of rats after i.v. injection. Two hours after injection, DM was diffusely distributed in nuclei and most parts of the cytoplasm of intestinal epithelial cells. The cytoplasmic immunoreactivity for DM was most pronounced in small granules of the apical cytoplasm. Sixteen hours after injection, DM immunostaining was by and large absent in the villous epithelium but persisted in the intestinal crypts. In addition, staining was also detected in endothelial cells, scattered cells of the lamina propria and in smooth muscle cells. After 5 days, only little staining for DM remained. Similar findings were made in the colon. In the gastric mucosa, DM accumulation persisted at 16 h in some glandular cells but was lost from the surface epithelium. No staining was detected in saline-injected control rats. The distribution of DM accumulation correlated partially with the distribution of apoptotic cells as detected by the TUNEL procedure. Our results pinpoint that DM may exert prolonged effects on glandular and regenerative cells of the gastrointestinal tract - an observation that may explain the gastrointestinal toxicity of the drug. It seems possible that DM accumulation in surface epithelial cells is rapidly cleared through drug transporters.
KW - Former LIFE faculty
KW - Daunomycin
KW - Immunocytochemistry
KW - Monoclonal antibody
KW - Rat
KW - Distribution
KW - Gastrointestinal tract
KW - Apoptosis
U2 - 10.1007/s00418-007-0314-6
DO - 10.1007/s00418-007-0314-6
M3 - Journal article
VL - 128
SP - 285
EP - 290
JO - Histochemistry and Cell Biology
JF - Histochemistry and Cell Biology
SN - 0948-6143
IS - 3
ER -
ID: 8099429