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1.
Br J Surg ; 107(9): 1192-1198, 2020 08.
Article in English | MEDLINE | ID: mdl-32335898

ABSTRACT

BACKGROUND: The right hepatic venous system consists of the right hepatic vein (RHV) and inferior RHVs (IRHVs). When the right posterior section is used as a graft for liver transplantation, understanding variations and relationships between the RHV and IRHVs is critical for graft venous return and hepatic vein reconstruction. This study aimed to evaluate variations in the hepatic veins and the relationships between them. METHODS: The medical records and CT images of patients who underwent hepatectomy as liver donors were assessed retrospectively. The relationship between the veins was evaluated by three-dimensional CT. RESULTS: The configuration of the posterior section was classified into one of eight types based on the RHV and IRHVs in 307 patients. Type 1a (103 of 307), type 1b (139 of 307) and type 2a (40 of 307) accounted for 91·9 per cent of the total. The diameter of the RHV extending towards the inferior vena cava had a significant inverse correlation with that of the IRHV (r2  = -0·615, P < 0·001). Type 1a, which had no IRHVs, had the RHV with the largest diameter; conversely, type 2a, which had a large IRHV, had the RHV with the smallest diameter. CONCLUSION: The hepatic venous system of the right posterior section was classified into eight types, with an inverse relationship between RHV and IRHV sizes. This information is useful for segment VII resection or when the right liver is used as a transplant graft.


ANTECEDENTES: El sistema venoso hepático derecho consiste en la vena hepática derecha (right hepatic vein, RHV) y las RHVs inferiores (IRHVs). Cuando se utiliza la sección posterior derecha hepática como injerto para el trasplante hepático, es fundamental conocer las variaciones e interrelaciones entre la RHV y las IRHVs para el retorno venoso del injerto y la reconstrucción de la vena hepática. El objetivo de este estudio fue determinar las variaciones en las venas hepáticas y sus interrelaciones. MÉTODOS: Se evaluaron retrospectivamente las historias clínicas y las imágenes de la tomografía computarizada de los pacientes que se sometieron a una hepatectomía como donantes vivos para trasplante hepático. La interrelación entre las venas se evaluó mediante imágenes de CT tridimensional. RESULTADOS: La configuración de la sección posterior clasificó a 307 pacientes en base a la RHV y a las IRHVs. Se clasificaron en 8 tipos, de los cuales el Tipo 1a (103/307), el Tipo 1b (139/307) y el Tipo 2a (40/307) representaron el 92% del total. El diámetro de la RHV que se extiende hacia la vena cava inferior presentó una correlación inversa significativa con la de las IRHV (r2: −0,632, P < 0,0001). El diámetro mayor de la RHV se observó en el Tipo 1a, que no presentaba IRHVs; por el contrario, el diámetro más pequeño se observó en el Tipo 2a que presentaba una IRHV grande. CONCLUSIÓN: El sistema venoso hepático de la sección posterior derecha se clasificó en 8 subtipos con una relación inversa entre los tamaños de la RHV y las IRHV. Esta información es útil cuando se practica una resección del segmento 7 o cuando se utiliza el hígado derecho como injerto para el trasplante.


Subject(s)
Hepatic Veins/diagnostic imaging , Tissue Donors , Hepatic Veins/anatomy & histology , Hepatic Veins/surgery , Humans , Imaging, Three-Dimensional , Liver/blood supply , Liver Transplantation/methods , Retrospective Studies , Tomography, X-Ray Computed
2.
Mol Psychiatry ; 21(11): 1613-1623, 2016 11.
Article in English | MEDLINE | ID: mdl-26830139

ABSTRACT

Caloric restriction (CR) is known to retard aging and delay functional decline as well as the onset of diseases in most organisms. Ghrelin is secreted from the stomach in response to CR and regulates energy metabolism. We hypothesized that in CR ghrelin has a role in protecting aging-related diseases. We examined the physiological mechanisms underlying the ghrelin system during the aging process in three mouse strains with different genetic and biochemical backgrounds as animal models of accelerated or normal human aging. The elevated plasma ghrelin concentration was observed in both klotho-deficient and senescence-accelerated mouse prone/8 (SAMP8) mice. Ghrelin treatment failed to stimulate appetite and prolong survival in klotho-deficient mice, suggesting the existence of ghrelin resistance in the process of aging. However, ghrelin antagonist hastened death and ghrelin signaling potentiators rikkunshito and atractylodin ameliorated several age-related diseases with decreased microglial activation in the brain and prolonged survival in klotho-deficient, SAMP8 and aged ICR mice. In vitro experiments, the elevated sirtuin1 (SIRT1) activity and protein expression through the cAMP-CREB pathway was observed after ghrelin and ghrelin potentiator treatment in ghrelin receptor 1a-expressing cells and human umbilical vein endothelial cells. Furthermore, rikkunshito increased hypothalamic SIRT1 activity and SIRT1 protein expression of the heart in the all three mouse models of aging. Pericarditis, myocardial calcification and atrophy of myocardial and muscle fiber were improved by treatment with rikkunshito. Ghrelin signaling may represent one of the mechanisms activated by CR, and potentiating ghrelin signaling may be useful to extend health and lifespan.


Subject(s)
Ghrelin/metabolism , Ghrelin/physiology , Sirtuin 1/metabolism , Aging/physiology , Animals , Caloric Restriction , Disease Models, Animal , Drugs, Chinese Herbal/metabolism , Drugs, Chinese Herbal/therapeutic use , Hypothalamus , Mice , Mice, Inbred ICR , Receptors, Ghrelin/genetics , Signal Transduction , Sirtuin 1/physiology
4.
Phys Rev A ; 51(3): R1746-R1749, 1995 Mar.
Article in English | MEDLINE | ID: mdl-9911898
5.
Biol Pharm Bull ; 16(12): 1297-300, 1993 Dec.
Article in English | MEDLINE | ID: mdl-8130783

ABSTRACT

Acyclothymidine (AcyT, 5-methyl-1-(2'-hydroxyethoxymethyl)uracil), a potent inhibitor of pyrimidine nucleoside phosphorylase (PyNPase), was co-administered with 5'-deoxy-5-fluorouridine (5'-DFUR), a PyNPase activating prodrug of 5-fluorouracil (5-FU), to rabbits. The absorption and pharmacokinetic parameters of 5'-DFUR and its active metabolite 5-FU, after administration of 5'-DFUR in combination with AcyT, were evaluated in the animals. Animals were given an oral or intravenous administration of 5'-DFUR (50 mg/kg) in combination with an equimolar dose of AcyT (40 mg/kg). The half-lives (t1/2) of 5'-DFUR and 5-FU in plasma were 16.8 and 11.5 min, respectively. AUC (area under the plasma concentration-time curve) of 5'-DFUR and 5-FU following the oral administration of 5'-DFUR (50 mg/kg) was 1710 and 24.3 micrograms.min/ml, respectively. After the oral co-administration of 5'-DFUR and AcyT (at a molar ratio of 1:1), the AUC values for 5'-DFUR and 5-FU increased to 2680 and to 121.1 micrograms.min/ml, respectively. However, this combination had little effect on the t1/2 of 5'-DFUR.


Subject(s)
Antineoplastic Agents/pharmacokinetics , Floxuridine/pharmacokinetics , Pentosyltransferases/antagonists & inhibitors , Uracil/analogs & derivatives , Administration, Oral , Animals , Antineoplastic Agents/administration & dosage , Chromatography, High Pressure Liquid , Drug Interactions , Floxuridine/administration & dosage , Fluorouracil/pharmacokinetics , Male , Pyrimidine Phosphorylases , Rabbits , Uracil/pharmacology
7.
Phys Rev A ; 45(11): 8019-8025, 1992 Jun 01.
Article in English | MEDLINE | ID: mdl-9906895
8.
Phys Rev A ; 45(7): 4799-4802, 1992 Apr 01.
Article in English | MEDLINE | ID: mdl-9907562
10.
Appl Opt ; 20(14): 2395-9, 1981 Jul 15.
Article in English | MEDLINE | ID: mdl-20332966

ABSTRACT

The polarization characteristics of an internal mirror cw 28-microm water vapor laser at zero magnetic field are studied. A typical 90? polarization flip is observed when one mirror is tilted from parallel alignment. When the mirrors are parallel, an off-axis mode oscillates in two orthogonal linear polarizations whose frequencies are separated by 290 kHz and whose intensities are distributed in two orthogonal patterns in a plane transverse to the laser axis.

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