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21.
J F Blickle P Reville F Stephan P Meyer C Demangeat R Sapin 《Hormones et métabolisme》1984,16(7):336-340
It is well established that glucagon plays an important role in the regulation of fuel supplies as its plasma level increases during the first days of a complete fast. However, it is not certain that glucagon is involved in the adaptation to chronic starvation. In the present study, this problem was investigated by the determination of the changes in the plasma glucagon level elicited by an i.v. glucose tolerance test followed by an i.v. arginine perfusion in 26 self starved patients suffering from anorexia nervosa (AN) and 14 control patients having only minor neurotic disorders. The basal plasma glucagon level tended to be higher in the AN patients than in the controls; but the difference was not statistically significant. Glucagon responses to glucose and arginine observed in the AN patients were not significantly different from those seen in the control patients. In the AN patients, the insulin response to both loads was reduced and the plasma GH level increased paradoxically after the glucose load, whereas it rose normally after the arginine load. It may be concluded that in chronic starvation by AN the regulation of fuel supplies depends mainly on decreased insulin and increased growth hormone secretion. The role of glucagon seems to be of minor importance in this condition. 相似文献
22.
Electrorotation—the spin of cells in rotating high frequency electric fields—has been used to investigate properties of human peripheral blood lymphocytes. The rotation spectra of lymphocytes deviate from those of single shell spheres. The deviations are caused by the electrical properties of the nucleus in the cell interior.Electrorotation allows the distinction between successfully stimulated lymphocytes and unstimulated cells after application of concanavalin A. Notwithstanding the fact that only a proportion of the cells will be mitogenically stimulated we detected an enhanced cell membrane conductivity for the whole cell population immediately after the addition of mitogen. 相似文献
23.
In this first of a series of papers concerning the theoretical analysis of rate theory models for ion transport through rigid pores, the case of vanishing interactions is investigated. "Rigidity" means that ions crossing membranes through pores see a fixed structure of the pores, not changing in time. A single pore is considered to be a sequence of (n + 1) activation barriers separated by n energy minima. The explicit analytical treatment is restricted to pores with regular internal barrier structure, including the nonequilibrium situation of an applied electric field. In this case the connection with continuum diffusion models is demonstrated by performing in the limit n leads to infinity (n = number of binding sites within the pores) the transition to continuum. Thus, from diffusion equations describing a discrete number of jumps, the corresponding diffusion-like partial differential equations and boundary conditions are generated. For regular pores, from the time dependent solutions of the discrete equations, the corresponding solutions of the continuum equations are explicitly generated. The time-dependent relaxation behaviour of the discrete model is in good agreement with the continuum model if one assumes more than two binding sites in the pores. 相似文献
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T S Elton C C Stephan G R Taylor M G Kimball M M Martin J N Durand S Oparil 《Biochemical and biophysical research communications》1992,184(2):1067-1073
A rat genomic Southern blot, probed with a type I angiotensin II receptor probe, demonstrated that two highly homologous type I angiotensin II receptors were present. A rat genomic library was subsequently screened and four clones were isolated. From restriction mapping, differential hybridization, polymerase chain reaction amplification and sequence analyses we have determined that there are two unique type I angiotensin II receptor genes. The first of these genes corresponds to the published rat vascular complementary DNA sequence; the second, corresponds to a novel receptor not previously described. 相似文献
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Roelof-Jan Oostra Stephan Kemp Pieter A. Bolhuis Elisabeth M. Sleeker-Wagemakers 《Human genetics》1996,97(4):500-505
Leber’s hereditary optic neuropathy (LHON) is a maternally inherited disorder of the optic nerves. It has been proposed that
the specific mutations in the mitochondrial DNA (mtDNA) that are associated with LHON require and X-chromosomally encoded
permissive factor in order to become expressed. This would explain both the preponderance of male patients and the fact that
most carriers of specific mtDNA mutations remain unaffected. Although linkage studies have been negative so far, the existence
of such a factor has not been ruled out. We investigated the genealogical data of 24 large LHON pedigrees and concluded that
the presumed X-linked factor would be recessively inherited and that at least 57% of the affected females would be heterozygous.
Therefore, these females must be the victim of nonrandom X-chromosomal inactivation (skewed lyonization). However, analysis
of X-chromosomal methylation patterns in 16 LHON-affected females revealed substantial skewing in only 15%–20% of cases, which
is not significantly different from the patterns in 49 controls. Moreover, we found the frequency of LHON in daughters of
affected heterozygous females to be twice to three times as high as in daughters of unaffected heterozygous females, which
cannot be explained by an X-chromosomally inherited factor. We conclude that the results of our investigations do not support
the hypothesis that LHON is a digenic disease with an X-linked factor being the main cause of loss of vision in the presence
of relevant mtDNA mutations.
Received: 1 June 1995 / Revised: 20 September 1995 相似文献
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