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G Pascal

Publications and source records attributed to G Pascal.

70 records · Page 4Linked to original sources

Schedule of protein ingestion and circadian rhythm of certain hepatic enzyme activities involved in glucose metabolism in the rat.

The circadian rhythms of liver glycogen, plasma glucose, corticosterone and insulin, and hepatic activity of PK, G6PDH, ME, Ac, CoA carbox. PEP-CK and GPT were studied in adult rats. Animals either received a mixed diet ad libitum (8% protein) or a protein meal (1.1 g protein) given at 05:00 or 17:00 h, with free access to a protein-free diet (separately fed). When the protein meal was ingested during the lighted period (17:00) the 24-hour average level of liver PEP-CK was greater than in rats consuming protein during darkness (05:00). In the latter case, modification of the circadian rhythm of liver glycogen and of circadian rhythm of liver PK, G6PDH, ME and Ac.CoA carbox. activity (increase of 24 h average level, extension of period of high activity, sudden increase after ingestion of protein meal) were observed. Conversely, the circadian rhythm of plasma insulin and corticosterone and of liver PEP-CK and GPT activity were only slightly affected by the mode of feeding.

Acetyl-CoA Carboxylase↗

[Dietary protein level and circadian variation of enzyme activities for glucose metabolism and lipogenesis in male rats (author's transl)].

One hundred and seven Wistar rats, 8 weeks old and weighing 180-200 g, were housed under conditions of controlled temperature (22 plus or minus 2 degrees) and lighting (light on from 07:00 to 19:00). They were divided into 2 groups and fed diets containing either 15 per cent cas-protein for 23 days. Food consumption was recorded every 2 hours for each animal during 48 hours. Four or five rats from each group were killed every 2 hours for 24 hours and the hepatic activities of PK (EC.2.7.1.40),G6P-DH (EC1.1.1.49), ME (EC1.1.1.40), Acetyl-CoA-carbox (EC.6.4.1.2.),PC(EC.6.4.1.1.), PEP-CK(EC.4.1.1.32), G6Pase (EC.3.1.3.9) and GPT (EC.2.6.1.2.) were measured...

Acetyl-CoA Carboxylase↗

Van der Woude syndrome. A case report.

We describe several members of a family with Van der Woude syndrome, a genetic and congenital malformation syndrome with autosomal dominant inheritance and 70% to 80% penetrance with variable expressivity. It is characterized by clinical signs localized to the face, such as bilateral or unilateral pits on conical elevations in babies or extensive depressions in adults, both in the vermilion border of the lower lip, with cleft lip, with or without cleft palate and uvula. Small accessory or heterotopic salivary glands empty into sinuses or fistulas in the lips. This eight member family had various clinical signs of the condition. All had cleft lip and palate. We studied the major characteristics of the eight patients and describe histopathologic and immunohistochemical features.

Cleft Lip↗