1976
DOI: 10.1016/s0016-5085(76)80057-1
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Morphometric Analysis of Rat Hepatocytes After Total Biliary Obstruction

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1978
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Cited by 83 publications
(29 citation statements)
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“…These data are in good agreement with those describing enhanced hepatic protein synthetic capacity in rats during the terminal portion of the life span. This study also confirmed the existence of a lobular gradient in the concentration of RER, i.e., the zone 1 hepatocytes contain slightly more of this membrane species than do centrolobular cells (Loud, 1968;Jones et al, 1976). Another quantitative morphological analysis mea- ANIMAL AGE (Months) Fig.…”
Section: Rough-surfaced Endoplasmic Reticulumsupporting
confidence: 73%
“…These data are in good agreement with those describing enhanced hepatic protein synthetic capacity in rats during the terminal portion of the life span. This study also confirmed the existence of a lobular gradient in the concentration of RER, i.e., the zone 1 hepatocytes contain slightly more of this membrane species than do centrolobular cells (Loud, 1968;Jones et al, 1976). Another quantitative morphological analysis mea- ANIMAL AGE (Months) Fig.…”
Section: Rough-surfaced Endoplasmic Reticulumsupporting
confidence: 73%
“…After 2-3 days of cholestasis, dilation and proliferation of small intralobar and interlobular bile ducts occur (11). Approximately 7 days after obstruction, fibroblast proliferation and leukocyte infiltration start and are followed by fibrosis and bile duct proliferation (19,20). In our study on histopathologic examination of the liver for 7 days after bile duct ligation mitotic activity, Councilman bodies, portal inflammation, ductular proliferation and fibrosis were observed in the DMSO and control groups.…”
Section: Discussionmentioning
confidence: 50%
“…Multiple factors may be involved in the ability of some bile acid species to accelerate HRP output into bile both in the intact rat [13,24] and in the isolated perfused liver [12]. However, although short exposure to bile acids may stimulate the TransCP, maintained elevated levels of bile acids could inhibit the activity of microtubule-based motor proteins [25], resulting in the reported impairment of microtubule-dependent vesicular transport during cholestasis [26,27]. Similarly, owing to the continuous exposure to high levels of bile acids that occurs during foetal liver development in the MOCP group [1], a certain degree of chronic inhibition of motor mechanisms responsible for vesicle movement along microtubules may exist.…”
Section: Discussionmentioning
confidence: 99%