Search PubMed⌕ Search

Biomedical subjects

M Guerre-Millo

Publications and source records attributed to M Guerre-Millo.

58 records · Page 4Linked to original sources

Maternofetal transfer of two benzodiazepines. Effect of plasma protein binding and placental uptake.

The influence of plasma protein binding on the maternofetal transfer of diazepam was studied in the perfused human placental lobule. Substitution of buffered salt perfusate in both maternal and fetal circuits for a perfusate with plasma proteins did not alter diazepam transfer significantly. Diazepam placental uptake was shown to be important in perfusion, with both types of perfusates. Comparison with the less liposoluble and less protein-bound benzodiazepine, fosazepam, revealed a marked difference in placental uptake but not in maternofetal transfer. In incubation studies, the kinetics of placental uptake confirmed this difference.

Blood Proteins↗

Transfer in vitro of three benzodiazepines across the human placenta.

A comparative study of the placental transfer to the foetus of three benzodiazepines was performed using a dual perfusion system of the human placental lobule. A transport fraction was calculated for each benzodiazepine and was compared with reference substances. Relative to antipyrine, the transport fraction of diazepam was 85%, and that of nordiazepam was 84%. The transport fraction of clorazepate represented only 20% of that of tritiated water. The relatively high transfer of diazepam and nordiazepam can be attributed to their high lipid solubility, and the lower transfer of clorazepate is due to its polar nature. It is suggested that in certain instances this benzodiazepine may be of especial value to obstetricians.

Anti-Anxiety Agents↗

Effects of photoperiod and feeding level on perirenal adipose tissue metabolic activity and leptin synthesis in the ovariectomized ewe.

Leptin is secreted by adipose tissue and plays a pivotal role in regulating both body energy homeostasis and reproductive function in rodents. Among livestock, sheep is a seasonal breeder whose reproductive period is initiated by short daylength. We show that plasma leptin and leptin gene expression in perirenal adipose tissue were decreased when ovariectomized Lacaune ewes were exposed to short days (8 versus 16 h light/d). This effect of the photoperiod occurred despite the nutritional status, with leptin levels lower in underfed than in refed ewes, and without significant changes in perirenal fat mass and adipocyte size. Plasma prolactin and leptin followed a similar pattern suggesting a relationship between the two hormones. These findings indicate, for the first time, that adipose tissue leptin is modulated by daylength independently of food intake, body fatness and gonadal activity. Furthermore, plasma non-esterified fatty acids of underfed ewes subjected to short days were more elevated than for underfed ewes on long days. On the other hand, refed ewes placed under long daylength tended to have a higher adipose tissue lipogenic activity than refed ewes on short days. We propose that these adaptations of leptin production and lipogenic activity with long photoperiod are of physiological significance for body fat deposition, which naturally occurs during long days when food is abundant. Conversely, a low leptin level during short days may enhance the sensitivity to food deprivation during the natural reproductive season, where any food shortage would decrease plasma leptin under a threshold critical for reproduction. Furthermore, in this situation, the observed enhanced ability to mobilize body fat may be related to the necessity to cope with energy shortage.

Adipose Tissue↗

[Recent data on the regulation of glucose transport and glucose transporters in insulin-sensitive tissues].

This review concerns the acute and long-term regulation of glucose transport. In insulin-sensitive tissues, the acute effect of insulin on this process occurs mainly through the translocation of glucose transport proteins (glucose transporters) from an intracellular pool to the plasma membrane. Some other factors are also able to modify acutely glucose transport by the translocation mechanism. However, recent data are reported which indicate that in addition, modifications of the glucose transporters activity are involved. The long-term regulation of the glucose transport capacity has been less studied. In different types of cultured cells, a role of two factors, glucose and insulin, has been clearly shown. The availability of cDNA probes encoding for glucose transporters, has given the opportunity to study the molecular regulation of glucose transport. However, it appears that different sub-types of glucose transport proteins exist which might be regulated in a specific manner depending on the cell-type and the regulatory factor. The existence of an insulin-sensitive glucose transporter is strongly suggested. The regulation of this protein, which could be specifically involved in insulin resistant physiopathological situations, remains to be studied.

Adipose Tissue↗