Effects of Multiple Doses of Dichloroacetate on GSTZ1 Expression and Activity in Liver and Extrahepatic Tissues of Young and Adult Rats

In newborn rats, lipoprotein lipase (LPL) activity was higher in the liver than in several other tissues, such as heart, diaphragm or lungs, and accounted for about 3% of total LPL activity in the body. There was no significant correlation between LPL activity in liver and in plasma. Thus transport of the enzyme from extrahepatic tissues was probably not the major source of LPL in liver. To study LPL biosynthesis directly, newborn rats were injected intraperitoneally with [35S]methionine, and LPL was isolated by immunoprecipitation and separation by SDS/polyacrylamide-gel electrophoresis. Radioactivity in LPL increased with a similar time course in all tissues studied, including the liver. Substantial synthesis of LPL was also demonstrated in isolated perfused livers from newborn rats, whereas synthesis was low in livers from adult rats. There was strong LPL immunofluorescence in livers from newborn rats, mainly within sinusoids and along the walls of larger vessels. This labelling disappeared after perfusion with heparin, which indicates that much of the enzyme is in contact with blood and can take part in lipoprotein metabolism.

Download Full-text

Induction of ceruloplasmin gene expression in rat lung during inflammation and hyperoxia

AJP Lung Cellular and Molecular Physiology ◽

10.1152/ajplung.1991.260.2.l68 ◽

1991 ◽

Vol 260 (2) ◽

pp. L68-L74 ◽

Cited By ~ 3

Author(s):

R. E. Fleming ◽

I. P. Whitman ◽

J. D. Gitlin

Keyword(s):

Gene Expression ◽

Relative Rate ◽

Rat Tissues ◽

Adult Rats ◽

Mrna Accumulation ◽

Adult Rat ◽

Mrna Content ◽

Extrahepatic Tissues ◽

Kinetics Of

To determine the effect of inflammation on extrahepatic ceruloplasmin gene expression we examined the ceruloplasmin mRNA content of adult rat tissues after endotoxin injection. Within 8 h of a dose of endotoxin ceruloplasmin mRNA content increased in the liver as expected and was also detectable in the lung. The effect of endotoxin was tissue specific because ceruloplasmin mRNA was not consistently detected in other extrahepatic tissues. The kinetics of ceruloplasmin mRNA accumulation in lung and liver tissue were similar with a maximum seven- to ninefold increase in ceruloplasmin mRNA content in each tissue within 24 h. The relative rate of ceruloplasmin gene transcription was increased in both tissues within 3 h of endotoxin, suggesting similar mechanisms of regulation of ceruloplasmin gene expression during inflammation. One cellular site of ceruloplasmin production in the inflamed lung was found to be the alveolar macrophage, which expressed the ceruloplasmin gene and synthesized ceruloplasmin protein in response to endotoxin in vitro. Because of these findings we also examined the effects of hyperoxia on ceruloplasmin gene expression. Exposure of adult rats to 95% O2 resulted in a five- to sixfold induction of ceruloplasmin mRNA in lung tissue within 46 h, and this response was time dependent, reaching maximum values at 86 h. Hyperoxic induction of ceruloplasmin mRNA was specific to the lung and not the result of systemic inflammation because hepatic ceruloplasmin mRNA content remained constant. These data indicate that the lung is a prominent site of ceruloplasmin gene expression during inflammation and hyperoxia and suggest that this protein may play a previously unappreciated role in pulmonary injury or repair.

Download Full-text

EFFECT OF STEROID HORMONES ON OESTROGEN-INDUCED UTERINE GLYCOGEN SYNTHESIS

Journal of Endocrinology ◽

10.1677/joe.0.0420065 ◽

1968 ◽

Vol 42 (1) ◽

pp. 65-77 ◽

Cited By ~ 7

Author(s):

HELENE C. CECIL ◽

J. BITMAN

Keyword(s):

Single Dose ◽

Testosterone Propionate ◽

Single Injection ◽

Initial Period ◽

Glycogen Synthesis ◽

Uterine Weight ◽

Adult Rats ◽

Control Value ◽

Multiple Doses ◽

Ovariectomized Adult Rats

SUMMARY Uterine weight, water, glycogen and glucose responses were analysed for 96 hr. after a single dose or daily doses of oestradiol given to ovariectomized adult rats. Six hr. after a single dose of oestradiol the uterine glycogen concentration doubled, reached a maximum of 4 times the control value at 12 hr. and then declined during the 16–48 hr. period. The ability of cortisol, deoxycorticosterone, progesterone, 17-ethyl-19-nortestosterone (Nilevar) or testosterone propionate to inhibit these responses was determined at 6 hr. (the initial period of maximum oestrogen action) and at 24 hr. (period of uterine glycogenolysis). A single injection of the antagonist given at the same time as oestrogen had no effect on the 6 hr. glycogen response. Pretreatment with cortisol, progesterone or testosterone propionate for 3 days caused a 30–50% inhibition of the oestrogen-induced increase. Multiple doses of testosterone propionate by itself were glycogenic. Single doses of the compounds appeared to be more effective at 24 hr. Multiple doses of cortisol, deoxycorticosterone, progesterone and testosterone propionate inhibited the 24 hr. glycogen response to oestradiol by 30–50%.

Download Full-text

Further Studies on the Ultrastructure of Harderian Gland in Adult Rats

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100051451 ◽

1974 ◽

Vol 32 ◽

pp. 288-289

Author(s):

Alfredo Feria-Velasco ◽

Guadalupe Tapia-Arizmendi

Keyword(s):

Fine Structure ◽

Domestic Fowl ◽

Animal Species ◽

Acinar Cells ◽

Harderian Gland ◽

Myoepithelial Cells ◽

The Other ◽

Albino Rats ◽

Adult Rats ◽

Cell Components

The fine structure of the Harderian gland has been described in some animal species (hamster, rabbit, mouse, domestic fowl and albino rats). There are only two reports in the literature dealing on the ultrastructure of rat Harderian gland in adult animals. In one of them the author describes the myoepithelial cells in methacrylate-embbeded tissue, and the other deals with the maturation of the acinar cells and the formation of the secretory droplets. The aim of the present work is to analize the relationships among the acinar cell components and to describe the two types of cells located at the perifery of the acini.

Download Full-text

Biodegradable polyester neuroprostheses promote the reconnection of separated peripheral nerve stubs

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100130109 ◽

1992 ◽

Vol 50 (2) ◽

pp. 1094-1095

Author(s):

Beverly L. Giammara ◽

Jennifer S. Stevenson ◽

Peggy E. Yates ◽

Robert H. Gunderson ◽

Jacob S. Hanker

Keyword(s):

Image Analysis ◽

Basement Membrane ◽

Periodic Acid ◽

Light And Electron Microscopy ◽

Computer Assisted ◽

Type Iii Collagen ◽

Image Analysis System ◽

Biodegradable Polyester ◽

Adult Rats ◽

Type Iv

An 11mm length of sciatic nerve was removed from 10 anesthetized adult rats and replaced by a biodegradable polyester Vicryl™ mesh sleeve which was then injected with the basement membrane gel, Matrigel™. It was noted that leg sensation and movement were much improved after 30 to 45 days and upon sacrifice nerve reconnection was noted in all animals. Epoxy sections of the repaired nerves were compared with those of the excised segments by the use of a variation of the PAS reaction, the PATS reaction, developed in our laboratories for light and electron microscopy. This microwave-accelerated technique employs periodic acid, thiocarbohydrazide and silver methenamine. It stains basement membrane or Type IV collagen brown and type III collagen (reticulin), axons, Schwann cells, endoneurium and perineurium black. Epoxy sections of repaired and excised nerves were also compared by toluidine blue (tb) staining. Comparison of the sections of control and repaired nerves was done by computer-assisted microscopic image analysis using an Olympus CUE-2 Image Analysis System.

Download Full-text

High-voltage EM description of the types and distribution of sensory endings in the inner conical body of the rat vibrissal follicle-sinus complex

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s042482010015959x ◽

1990 ◽

Vol 48 (3) ◽

pp. 410-411

Author(s):

Tony M. Mosconi ◽

Min J. Song ◽

Frank L. Rice

Keyword(s):

Mammalian Species ◽

Dorsal Side ◽

Hair Shaft ◽

Sensory Innervation ◽

Conical Body ◽

Adult Rats ◽

Perpendicular Plane ◽

Ultrastructural Studies ◽

Unmyelinated Axons ◽

Sensory Endings

Whiskers or vibrissal follicle-sinus complexes (F-SCs) on the snouts of many mammalian species are structures that have complex, dense sensory innervation. The innervation of F-SCs is remarkably similar in all species with the exception of one site - the inner conical body (ICB). The ICB is an elongated cylindrical structure that encircles the hair shaft near the neck of the follicle. This site has received only cursory attention in ultrastructural studies of the F-SCAdult rats were perfused after the method of Renehan and Munger2. F-SCs were quartered longitudinally and embedded separately in Epon-Araldite. Serial 0.25 μm sections were cut in either the longitudinal or perpendicular plane through the ICB and examined with an AEI EM7 1.2 MV HVEM (Albany, NY) at 1000 KV. Sensory endings were reconstructed from serial micrographs through at least 20 μm in the longitudinal plane and through 10 μm in the perpendicular plane.From two to six small superficial vibrissal nerves converge upon the neck of the F-SC and descend into the ICB. The nerves branch into smaller bundles of myelinated and unmyelinated axons along the dorsal side of the hair shaft.

Download Full-text