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31.
Takeshi Minami Masayo Ichii Yoshiyuki Tohno Setsuko Tohno Masako Utsumi Masa-oki Yamada Yuko Okazaki 《Biological trace element research》1996,55(1-2):199-205
The purpose of this study was to determine the extent of aluminum (Al) accumulation in the human aorta and cerebral arteries.
The Al contents in the aortae and in the cerebral arteries from 23 human subjects was determined by inductively coupled plasma
atomic emission spectrophotometry (ICP-AES). The subjects' age range was 45–99-yr-old; 15 of the subjects were males and 8
were females. Al was detected in twelve aortae and in six cerebral arteries, when the entire specimen was analyzed. Two specimens
where Al was found in the cerebral arteries contained no Al in the aorta. No relationship to the subject's sex was found.
When related to age, two groups were established. Group L (45–75 yr old) and group H (>75 yr old), which exhibited aortal
Al concentrations of 33.3 and 72.7%, respectively. When the aortic wall was dissected into the tunica intima, media, and adventitia,
Al was found mainly in the tunica media. In the aorta, significant relationships were found between Al and phosphorus (P)
levels (r=0.801,p<0.01) and between Al and calcium (Ca) (r=0.661,p<0.05). We have concluded that Al accumulation is age-dependent and that it occurs both in the aorta and in the cerebral artery.
In the aorta, accumulation occurs mainly in the tunica media. Both P and Ca appear to enhance aortal Al accumulation. 相似文献
32.
The lungs of three silvered lutongs (Presbytis cristata) were examined. The right and left lungs have the dorsal, lateral, ventral, and medial bronchiole systems, which arise from
the corresponding sides of both bronchi, respectively. Bronchioles in the dorsal and lateral bronchiole systems are well developed,
whereas those in the ventral and medial bronchiole systems are poorly developed and lack some portions. According to the fundamental
structure of bronchial ramifications of the mammalian lung (Nakakuki, 1975, 1980), the right lung consists of the upper, middle, lower, and accessory lobes, whereas the left lung consists of
a bilobed middle lobe and a lower lobe, in which the right upper lobe is extremely well developed. The right pulmonary artery
runs across the ventral side of the right upper lobe bronchiole, and then across the dorsal side of the right middle lobe
bronchiole. Initially it runs along the lateral side of the right bronchus and then gradually comes to run along the dorsal
side. During its course, it gives off branches which run mainly along the dorsal or lateral side of the bronchiole. The left
pulmonary artery runs across the dorsal side of the left middle lobe bronchiole, and then follows the same course as that
in the right lower lobe. The pulmonary veins run medially or ventrally to the bronchioles, and finally enter the left atrium
as four or five large veins. 相似文献
33.
L. H. Clapp A. M. Gurney N. B. Standen P. D. Langton 《The Journal of membrane biology》1994,140(3):205-213
Tension and patch clamp recording techniques were used to investigate the relaxation of rabbit pulmonary artery and the properties of the K+ current activated by levcromakalim in isolated myocytes. Under whole-cell voltage clamp, holding at –60 mV in symmetrical 139 mm K+, levcromakalim (10 m) induced a noisy inward current of –116 ± 19 pA (n = 13) which developed over 1 to 2 min. This current could be blocked by either glibenclamide (10 m) or phencyclidine (5–50 M) and was unaffected when extracellular Ca2+ was removed. Both these drugs inhibited the levcromakalim-induced relaxation of muscle strips precontracted with 20 mm [K+]
o
. Application of voltage ramps in symmetrical 139 mm K+ confirmed that the levcromakalim-induced current was carried by K+ ions and was weakly voltage dependent over the potential range from –100 to +40 mV.The unitary current amplitude and density of the channels underlying the levcromakalim-activated whole-cell K+ current was estimated from the noise in the current record. We estimate that levcromakalim caused activation of around 300 channels per cell, with a single channel current of 1.1 pA, corresponding to a slope conductance of about 19 pS. Furthermore, cells dialyzed with an ATP-free pipette solution developed a large noisy inward current at –60 mV, which could subsequently be blocked by flash photolysis of caged ATP. Analysis of the noise associated with this current indicated that the single channel amplitude underlying the ATP-blocked current was 1.4 pA, a value similar to that estimated for the levcromakalim-induced current. We conclude that the conductance of this ATP-sensitive channel is likely to be small under physiological conditions and that it is present at low density.We thank SmithKline & Beecham for the gift of levcromakalim, ICI Pharmaceuticals for the gift of charybdotoxin and Prof. D. Colquhoun for the noise analysis programs. We also thank Mr. R. Davey for technical assistance with tension experiments. This work was supported by the British Heart Foundation and the Wellcome Trust. L.H.C. is a Wellcome Research Fellow and P.L. is an intermediate fellow of the BHF. 相似文献
34.
Raquel Fernández-Durango José A. de Juan Horatio Zimman Francisco J. Moya Mario Garcia de la Coba Arturo Fernández-Cruz 《Journal of neurochemistry》1994,62(4):1482-1488
Abstract: Specific endothelin (ET) binding sites were characterized in membranes prepared from human cerebral cortices using binding assay and cross-linking analysis. The presence of immunoreactive (IR) ET-1 was studied by radioimmunoassay. Saturation binding experiments revealed that the K D and B max for 125 I-ET-1 and 125 l-ET-3 to membranes from gray matter were 25 ± 6 pM and 115 ± 15 fmol/mg of protein and 24 ± 5 p M and 108 ± 13 fmol/mg of protein, respectively. Similar results were obtained for white matter. In the presence of 10 n M sarafotoxin-6c, which is selective for ETB receptors, 125 I-ET-1 and 125 l-ET-3 binding was totally abolished. However, in the presence of 1 μ M BQ123, which is selective for ETA receptors, both bindings were not affected. These results suggest that the human cerebral cortex contains only ETB receptors. Cross-linking of 125 I-ET-1 and 125 l-ET-3 to membranes with disuccinimidyl suberate resulted in the labeling of two bands of 48 and 31 kDa. Concentrations of IR-ET-1 in the gray and white matter were 7.0 ± 3.2 and 2.5 ± 1.7 fmol/g wet weight, respectively. The demonstration of high-affinity ETB receptors and the presence of IRET-1 suggest that the peptide may act as a neurotransmitter or neuromodulator in the human cerebral cortex. 相似文献
35.
内皮素对失血性休克鼠脑微循环的影响及尼莫地平、川芎嗪的治疗作用 总被引:1,自引:1,他引:0
利用大鼠颅骨开窗观察软脑膜微循环的方法研究了内皮素(ET-1)10-10-10-7mol/L对软脑膜微循环的影响以及失血性休克时软脑膜对ET-1的反应性。并用10-7mol/L造成失血性休克后脑血管痉挛的模型,观察尼莫地平、川芎嗪、654-2对内皮素引起血管痉挛的治疗作用。10-9、10-8和10-7mol/L3种浓度ET-1可使软脑膜小动脉、细动脉强烈收缩,收缩率分别为27.7%、46.8%、78.5%,其收缩强度与ET-1的浓度有关。对静脉的作用不明显。10-10mol/LET-1可使细动脉轻度扩张。出血性休克时,软脑膜血流明显减慢,小动脉、细动脉管径对ET-1的收缩作用更敏感,脑组织血流明显减少。尼莫地平具有较好的拮抗ET-1引起软脑膜动脉的收缩和改善局部微循环的作用。川芎嗪也能拮抗ET-1引起软脑膜动脉的收缩,但作用较尼莫地平弱。654-2不能缓解ET-1对软脑膜动脉的收缩作用。 相似文献
36.
37.
通过对80例急性脑出血死亡组分析,发现死于脑疝的占62.5%,脑疝与一种或二种以上合并症同存者占77.5%,显著高于存活组(P<0.01).它们互为因果,加速死亡。因此,应重视早期或超早期采用简易定向锥颅脑内血肿碎吸术吸除血肿,同时注意维持生命体征稳定,加强脱水降颅压,预防、控制合并症等综合治疗。且要全面分析,相互兼顾,正确处置。这是帮助机体渡过调控障碍难关,挽救生命的有效治疗措施。 相似文献
38.
Louis Faso Richard S. Trowbridge Wei Quan Xiu-Lan Yao Edmund C. Jenkins Alma Maciulis Thomas D. Bunch Henry M. Wisniewski 《In vitro cellular & developmental biology. Animal》1994,30(4):226-235
Summary A strain of cerebral endothelial cells was established from isolated cortical microvessels of caprine brain. These cells,
which are referred to as ECl cells, can be routinely subcultured to 32 passages without the loss of differentiated morphologic
and immunologic traits. The ability to routinely subculture ECl cells is an important asset, given that isolated cerebral
endothelial cells in mammals generally lose their differentiated traits after only 2 to 3 passages.
ECl cells were shown to contain Factor VIII-related antigen, which is a specific marker for cells of endothelial origin. ECl
cells morphologically demonstrated a scarcity of pinocytotic vesicles on their apical surfaces, a lack of trans-cytoplasmic
vesicles, and the ability to form in culture confluent monolayers with tight junctional complexes. Therefore, ECl cells possess
specific antigenic and ultrastructural features which classify them as being small vessel endothelial cells of the blood-brain
barrier type. Cytogenetic evaluation of ECl cells demonstrated a normal female goat 60,XX karyotype and confirmed the apparent
non-transformed nature of ECl cells due to the lack of chromosome abnormalities or rearrangements. Using scanning electron
microscopy, ECl cells were also shown to form confluent monolayers on mixed nitrocellulose filters, a feature that will enable
the development of an in vitro system to study trans-endothelial transport. Given that ECl cells are readily subcultured and
grow well on nitrocellulose filters, and that they resemble cerebral endothelium in vivo, it seems evident that ECl cells
can be used as a versatile model for the study of blood-brain barrier function, regulation, and pathology. 相似文献
39.
Trinidad Hernández-Caselles José Villalaín Juan C. Gómez-Fernández 《Molecular and cellular biochemistry》1993,121(2):119-126
The roles of sulfhydryl and disulfide groups in the specific binding of synthetic cannabinoid CP-55,940 to the cannabinoid receptor in membrane preparations from the rat cerebral cortex have been examined. Various sulfhydryl blocking reagents including p-chloromercuribenzoic acid (p-CMB), N-ethylmaleimide (NEM), o-iodosobenzoic acid (o-ISB), and methyl methanethiosulfonate (MMTS) inhibited the specific binding of [3H]CP-55,940 to the cannabinoid receptor in a dose-dependent manner. About 80–95% inhibition was obtained at a 0.1 mM concentration of these reagents. Scatchard analysis of saturation experiments indicates that most of these sulfhydryl modifying reagents reduce both the binding affinity (Kd) and capacity (Bmax). On the other hand, DL-dithiothreitol (DTT), a disulfide reducing agent, also irreversibly inhibited the specific binding of [3H]CP-55,940 to the receptor and about 50% inhibition was obtained at a 5 mM concentration. Furthermore, 5mM DTT was abelt to dissociate 50% of the bound ligand from the ligand-receptor complex. The marked inhibition of [3H]CP-55,940 binding by sulfhydryl reagents suggests that at least one free sulfhydryl group is essential to the binding of the ligand to the receptor. In addition, the inhibition of the binding by DTT implies that besides free sulfhydryl group(s), the integrity of a disulfide bridge is also important for [3H]CP-55,940 binding to the cannabinoid receptor. 相似文献
40.
Paul M. Gross Madan G. Joneja Judy J. Pang Trevor M. Polischuk Steven W. Shaver Dan S. Wainman 《Cell and tissue research》1993,272(1):79-88
We applied scanning electron microscopy combined with imaging and morphometric techniques to analyze the dorsal topography and morphology of short portal vessels linking the capillary beds of the pituitary neural and anterior lobes in adult male albino rats. The pituitary microvasculature was replicated by intracarotid injection of Batson's No. 17 compound producing plastic casts that were advantageous for comprehensive morphometric analyses using an imaging device. The analysis revealed the existence of two types of portal vessels having quantitatively different morphological properties. The bilateral venular plexus of 3–4 vessels located at the base of the infundibular stalk (each venule measuring 300 m in length and 32 m in diameter) appears to be the major part of the short portal system in the dorsum of the rat pituitary gland. Narrower capillary-like shunt vessels (6.8 m in diameter), of about the same length as the venules, were situated throughout other subregions of the intermediate lobe cleft. The short portal vessels of both types made direct anastomoses with the capillary networks in the neural and anterior lobes. The neural lobe capillaries were twice as numerous (1324 per mm2), and only half as wide (6.2 m), as the sinusoidal capillaries in the anterior lobe (density of 637 per mm2; diameter of 13.7 m). The topographical position of the portal venular system suggests that the caudolateral subregions of the pituitary neural and anterior lobes have a functional relationship dependent on rapid interlobe transfer of neurohumoral factors such as hormones via the portal blood. This process appears to be supplemented throughout the rest of the cleft between the two lobes by a small number of capillary shunts that supply the epithelial cell lobules of the intermediate lobe in situ. The findings collectively indicate that this portal system provides a constant stream of neurohumoral information that is shared moment-by-moment between the pituitary neural and anterior lobes. 相似文献