Heterogeneity of kinetic parameters of enzymes in situ in rat liver lobules

1995 ◽  
Vol 103 (2) ◽  
pp. 93-101 ◽  
Author(s):  
C. J. F. Noorden ◽  
G. N. Jonges
Keyword(s):  
Kinetic Parameters ◽  
Rat Liver

scholarly journals In situ kinetic parameters of glucose-6-phosphatase in the rat liver lobulus.

1992 ◽  
Vol 267 (7) ◽  
pp. 4878-4881
Author(s):  
G.N. Jonges ◽  
C.J. Van Noorden ◽  
W.H. Lamers
Keyword(s):  
Kinetic Parameters ◽  
Rat Liver

scholarly journals Microbial N2O consumption in and above marine N2O production hotspots

2020 ◽  
Author(s):  
Xin Sun ◽  
Amal Jayakumar ◽  
John C. Tracey ◽  
Elizabeth Wallace ◽  
Colette L. Kelly ◽  
...  
Keyword(s):  
Kinetic Parameters ◽  
Substrate Affinity ◽  
N2o Production ◽  
Anoxic Waters ◽  
Production And Consumption ◽  
Consumption Rates ◽  
Anoxic Zones ◽  
First Time ◽  
Microbial N

AbstractThe ocean is a net source of N2O, a potent greenhouse gas and ozone-depleting agent. However, the removal of N2O via microbial N2O consumption is poorly constrained and rate measurements have been restricted to anoxic waters. Here we expand N2O consumption measurements from anoxic zones to the sharp oxygen gradient above them, and experimentally determine kinetic parameters in both oxic and anoxic seawater for the first time. We find that the substrate affinity, O2 tolerance, and community composition of N2O-consuming microbes in oxic waters differ from those in the underlying anoxic layers. Kinetic parameters determined here are used to model in situ N2O production and consumption rates. Estimated in situ rates differ from measured rates, confirming the necessity to consider kinetics when predicting N2O cycling. Microbes from the oxic layer consume N2O under anoxic conditions at a much faster rate than microbes from anoxic zones. These experimental results are in keeping with model results which indicate that N2O consumption likely takes place above the oxygen deficient zone (ODZ). Thus, the dynamic layer with steep O2 and N2O gradients right above the ODZ is a previously ignored potential gatekeeper of N2O and should be accounted for in the marine N2O budget.

scholarly journals HIGH-YIELD PREPARATION OF ISOLATED RAT LIVER PARENCHYMAL CELLS

1969 ◽  
Vol 43 (3) ◽  
pp. 506-520 ◽  
Author(s):  
M. N. Berry ◽  
D. S. Friend
Keyword(s):  
Gap Junctions ◽  
Rat Liver ◽  
Structural Integrity ◽  
Cell Injury ◽  
High Yield ◽  
Isolated Cells ◽  
Nylon Mesh ◽  
Parenchymal Cells

A new technique employing continuous recirculating perfusion of the rat liver in situ, shaking of the liver in buffer in vitro, and filtration of the tissue through nylon mesh, results in the conversion of about 50% of the liver into intact, isolated parenchymal cells. The perfusion media consist of: (a) calcium-free Hanks' solution containing 0.05% collagenase and 0.10% hyaluronidase, and (b) magnesium and calcium-free Hanks' solution containing 2 mM ethylenediaminetetraacetate. Biochemical and morphologic studies indicate that the isolated cells are viable. They respire in a medium containing calcium ions, synthesize glucose from lactate, are impermeable to inulin, do not stain with trypan blue, and retain their structural integrity. Electron microscopy of biopsies taken during and after perfusion reveals that desmosomes are quickly cleaved. Hemidesmosome-containing areas of the cell membrane invaginate and appear to pinch off and migrate centrally. Tight and gap junctions, however, persist on the intact, isolated cells, retaining small segments of cytoplasm from formerly apposing parenchymal cells. Cells which do not retain tight and gap junctions display swelling of Golgi vacuoles and vacuoles in the peripheral cytoplasm. Cytoplasmic vacuolization in a small percentage of cells and potassium loss are the only indications of cell injury detected. By other parameters measured, the isolated cells are comparable to normal hepatic parenchymal cells in situ in appearance and function.

In Situ Hybridization of Ha-RAS during Rat Liver Carcinogenesis

1991 ◽  
pp. 111-118
Author(s):  
V. Préat ◽  
Y. Nizet ◽  
S. Haesen ◽  
M. Roberfroid
Keyword(s):  
In Situ Hybridization ◽  
Rat Liver ◽  
Liver Carcinogenesis
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