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Biomedical subjects

H Bouissou

Publications and source records attributed to H Bouissou.

At least 109 records · Page 6Linked to original sources
PubMed1976

[Correlation between age, arteriosclerosis and elastinolytic activity of human aorta wall].

An elastolytic protease was isolated recently from human and animal aortic wall. We report here the positive correlation between the activity of human aortic elastase, the degree of atherosclerosis and age. These two parameters appear to influence independently and in an additive fashion the level of aortic elastase. There appears to be an increasing synthesis and/or liberation of aortic elastase with age. This process is accelerated in the presence of arteriosclerosis. It appears probable that the increasing elastolytic activity is mainly responsible for the fregmentation and lysis of the elastic fibers with age and arteriosclerosis as observed with histochemical techniques.

Aging↗
PubMed1976

[Cutaneous cholesterol and phospholipids in atherosclerosis].

Previously, a lesion parallelism between skin and vascular wall was established when aging. Besides, we have pointed out a significant increase of cutaneous sterols rate along with aortic atheromatous stage. This study brings forward a new fact: increase (not significant because wanting much more examples) of cutaneous squalene rate varying with atheroma intensity, but reversely stability of total phospholipids with their various fractions.

Arteriosclerosis↗
PubMed1976

[Incorporation of 32P-orthophosphate in aortic phospholipids in chronic lathyrims in the rat].

Study of 32P orthophosphate incorporation into rat aortic phospholipids after B.A.P.N. treatment, which was followed or not by a lipid-supplemented diet (4.5 p. 100 cholesterol and 37 p. 100 butter). The 32P orthophosphate turnover in the total phospholipid was twice as slow among B.A.P.N.-treated rat than among control-rat. Such a decrease of the 32P orthophosphate turnover could be found as well in phosphatidylethanolamines, phosphatidylcholines and lysophosphatidylcholines. Sphingomyelins showed a very weak metabolic activity among two groups of rats. 32P orthophosphate incorporation into inositolphosphatides was slowed down by B.A.P.N. treatment. Maximal specific activity of inositolphosphatides after injection of 32P orthophosphate was reached within 4 hours in control rats, and 8 hours in B.A.P.N.-treated rats. Three months after the end of B.A.P.N. treatment, no difference in specific activity could be found between control-rats and B.A.P.N.-treated rats. Lipid supplemented diet modified the metabolic activity of phospholipids equally in control rats and B.A.P.N.-treated rats. Specific activity decrease in total phospholipids, phosphatidylcholines, phosphatidylethanolamines, and increase in lysophosphatidylcholines were noted in both groups of animals under a high rat diet. These modifications of the metabolic activity of different phospholipids were most marked fourteen hours after 32P orthophosphate injection. B.A.P.N. treatment only slowed the incorporation of 32P phosphate into phospholipids. Administration of a single lipid supplemented diet or a diet associated with B.A.P.N. treatment induced a slower turnover of phosphatidylcholines and phosphatidylethanolamines, and a faster turnover of lysophosphatidylcholines.

Aminopropionitrile↗
PubMed1976

[Structural and biochemical alterations of human diabetic dermis studied by H-lysine incorporation and microscopy].

The alteration of the structural organization of dermal connective tissue was studied by light and electron microscopy and by biochemical techniques in normal human and in diabetic patients using skin biopsies. Part of the tissue was used for light and electron microscopy, the rest was incubated in the presence of 3H-lysine for four hours. The 3H-lysine labelled biopsies were submitted to a sequential extraction procedure in order to obtain representative macromolecular fractions containing the matrix macromolecules. The extracts were analyzed for their chemical composition and radioactivity. Electron microscopy revealed ultrastructural modifications of the fibroblasts, of the collagen and elastic fibers in the diabetic dermis. Fibroblasts contained an increased amount of electron dense deposits in the cytoplasm and dilated endoplasmic reticulum. The collagen bundles were dissociated. Elastic fibers under the epithelial basal laminae were fragmented or absent. The incorporation pattern of 3H-lysine into these macromolecular fractions was different in the normal and diabetic skin biopsies. The percentage of total radioactivity incorporated increased significantly in the 1M CaCl2 extractable fraction an in the 6M urea extractable fraction and decreased significantly in the collagenase and elastase extracts in diabetic skin biopsy. These results demonstrate the existence of morphological and biochemical alterations in diabetic connective tissue (dermis) reflecting alterations in the relative rates of synthesis and/or degradation of the intercellular matrix macromolecules as well as of their microarchitectural arrangement.

Adolescent↗
PubMed1976

[Gallium sulfate and skin allografts in the mouse].

Survival of skin allografts in mice are prolonged when these animals are injected subcutaneously with gallium sulfate before and after the grafting. The average survival is then 17, 2 days whereas it is 12,5 days for controls. For mice treated with an immunodepressive drug such as cortisone acetate average survival is 13,4 days; it is 17 days when cortisone has been added to the metallic salt.

Animals↗
PubMed1976

[Chronic lathyrism, prolonged hyperlipidic diet, and atheroma in the rat].

Deep, constant, extensive atherosclerosis can be experimentally induced on rats that are atheroresistant. Two main factors are involved in this experimentation; parietal alteration following chronic intoxication with BAPN (9 weeks) and a metabolic factor with hyperlipidic diet, but this metabolic damage should be sustained for a long time (40 weeks).

Aminopropionitrile↗
PubMed1975

[Value and duration of the bone localization of gallium in the mouse].

Gallium was administered subcutaneously to mice, and was found to be localized essentially in the skeleton. It was measured in the bones of animals given daily injections of gallium sulfate. There was little or no mortality. The amount of gallium found rose with the number of injections, and was greater when higher doses were injected. Elimination was very low after cessation of treatment. Results were used to study the action of gallium on cutaneous allografts in mice.

Animals↗