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81.
Shuzo Miyamoto Yoshihiro Matsuda Shin-ichiro Sano Hiroshi Shiraki Hachro Nakagawa 《Neurochemical research》1992,17(7):723-727
The activity of ammoniagenesis from guanine nucleotides was found to increase significantly in rat brain after infusion of kainic acid into the striatum. Among the enzymes involved in degrading guanine nucleotides, nucleoside diphosphatase was markedly increased in the lesioned striatum. The enzyme activity began to increase 2 days after the infusion, and reached the maximum on the 13th day, the level being 4 times as high as that of the intact contralateral region. The increased activity was due to Type L enzyme, judging from its substrate specificity. Puromycin and cycloheximide inhibited this increase, indicating that the increased activity resulted from an increase in the net synthesis of the enzyme. These findings suggest that Type L NDPase might play some important roles in gliosis after neuronal lesion. 相似文献
82.
Antipsychotics represent high affinity for sigma receptors and sigma-like drugs often have the psychotomimetic properties. Besides, the receptors are unevenly distributed in human brain. These findings suggest that sigma receptors might be involved in the pathophysiology of schizophrenia. Sigma receptors in rat and human brain were measured with [3H]-1, 3, di-o-tolylguanidine (DTG) and non-specific binding of [3H]DTG was determined in the presence of 10–5M haloperidol. Monovalent and divalent cations strongly inhibited [3H]DTG binding. Glutamate, aspartate and glycine also decreased the binding to human cerebral membranes. With post-mortem brain samples from 12 schizophrenics and 10 controls, sigma receptors were measured in 17 areas of cerebral cortex. Sigma receptors binding showed the regional differences in the cortex, but no significant differences between schizophrenics and controls were observed except the superior parietal cortex where the binding significantly increased in the schizophrenic group. These results suggest that sigma receptors in cerebral cortices might not be directly concerned with the pathophysiological role in schizophrenia.Dedicated to Dr. Morris Aprison. Received too late for publication in special issue. 相似文献
83.
实验在α氯醛糖和氨基甲酸乙酯混合麻醉的大鼠中进行。脑室内注射高张盐水(icv.HS)后,肾血浆流量、肾小球滤过率、尿量、尿钠排出量、尿钾排出量和渗透物质清除率均增加,游离水清除率下降。去除垂体后,icv.HS不再能引起上述肾脏反应。另外给大鼠静脉注射血管升压素(VP)拮抗剂(V_1和V_2受体拮抗剂),并不能削弱上述icv.HS引起的肾脏反应。脑室内注射高张盐水后,尿中多巴胺(DA)排出量无显著增多;给予多巴脱羧酶抑制剂苄丝肼也不能削弱icv.HS引起的肾脏反应。上述实验结果表明,在本实验条件下刺激脑内渗透压感受器引起的肾脏反应依赖于垂体的完整性,但看来并不依赖于外周的VP和DA,故垂体通过何种机制介导icv.HS引起上述肾脏反应,有待于进一步的研究。 相似文献
84.
Klaas J. Lusthof Nicolaas J. del Mol Wilma Richter Lambert H.M. Janssen John Butler Brigid M. Hoey Willem Verboom David N. Reinhoudt 《Free radical biology & medicine》1992,13(6):599-608
The formation of reactive oxygen intermediates (ROI) during redox cycling of newly synthesized potential antitumor 2,5-bis (1-aziridinyl)-1,4-benzoquinone (BABQ) derivatives has been studied by assaying the production of ROI (superoxide, hydroxyl radical, and hydrogen peroxide) by xanthine oxidase in the presence of BABQ derivatives. At low concentrations (< 10 microM) some BABQ derivatives turned out to inhibit the production of superoxide and hydroxyl radicals by xanthine oxidase, while the effect on the xanthine-oxidase-induced production of hydrogen peroxide was much less pronounced. Induction of DNA strand breaks by reactive oxygen species generated by xanthine oxidase was also inhibited by BABQ derivatives. The DNA damage was comparable to the amount of hydroxyl radicals produced. The inhibiting effect on hydroxyl radical production can be explained as a consequence of the lowered level of superoxide, which disrupts the Haber-Weiss reaction sequence. The inhibitory effect of BABQ derivatives on superoxide formation correlated with their one-electron reduction potentials: BABQ derivatives with a high reduction potential scavenge superoxide anion radicals produced by xanthine oxidase, leading to reduced BABQ species and production of hydrogen peroxide from reoxidation of reduced BABQ. This study, using a unique series of BABQ derivatives with an extended range of reduction potentials, demonstrates that the formation of superoxide and hydroxyl radicals by bioreductively activated antitumor quinones can in principle be uncoupled from alkylating activity. 相似文献
85.
Effect of pyridoxine on tumor necrosis factor activitiesin vitro 总被引:1,自引:0,他引:1
Clinical trials with tumor necrosis factor (TNF) as an antitumor agent have so far given rather disappointing results. In this study we show that the naturally occuring vitamin B6 compound, pyridoxine, enhances TNF-induced cytolysis of three subclones of a mouse fibrosarcoma cell line (WEHI 164). The degree of pyridoxine-induced enhancement of TNF cytotoxicity seems to be dependent on the cells sensitivity to TNF, as the enhancement was much more pronounced in the relatively TNF resistant subclone act-R(cl.12)-WEHI 164, than in the very TNF sensitive subclone WEHI 164 clone 13. Furthermore, our study shows that pyridoxine, in contrast to its enhancing effect on TNF-induced cytotoxicity, rather inhibits TNF-induced growth of human FS-4 fibroblasts. Pyridoxine also enhances lymphotoxin (LT)-induced tumor cell killing and inhibits LT-induced fibroblast growth. Pyridoxine is a relatively non-toxic agentin vivo. Our results suggest that a combination of TNF and pyridoxine may be more efficient than TNF alone, in the treatment of cancer patients. 相似文献
86.
Kunio Nakagawa Norio Omori Kahoko Hashimoto Tetsuya Yamamoto Takashi Tsunoda Tadao Nose 《Biotherapy》1992,4(2):109-115
Thein vitro effect of a combined treatment with lymphokine activated killer (LAK) cell and radiation therapy on rat brain tumor was examined using51Cr release assay. The tumor cell-line used in this experiment was 9L rat brain tumor derived from a Fischer 344 rat. LAK cells were obtained by culturing rat lymphocytes with recombinant human interleukin 2 for at least 3 days. The cytotoxic activity of the LAK cells was examined by51Cr release assay. Irradiation was done by exposing the microtiter plate in which the15Cr labeled 9L cells and LAK cells were cultured to a137Cs gamma cell unit. Without irradiation, there was 18% cytotoxicity in the 1:100 tumor-to-LAK cell ratio specimen after 24 hrs cocultivation. However, if 5 Gy of irradiation was given, followed by 12 hrs incubation, the cytotoxicity was enhanced significantly at the same cell ratio (30%). This enhancement effect was the most prominent when the cell ratio was 1:100 and the irradiation dose was 5 Gy. To generate the enhancement effect, an incubation time of over 8 hrs both before and after irradiation was required. The supernatant of the LAK cells showed 19.8% and 11.4% cytotoxicity with and without irradiation, respectively. This result indicates the participation of a cytotoxic factor released from LAK cells.This work is supported in part by grant from Univeristy of Tsukuba Project Research. 相似文献
87.
Antigen-specific,MHC-unrestricted T cells 总被引:2,自引:0,他引:2
Olivera J. Finn 《Biotherapy》1992,4(4):239-249
The published record suggests that in the majority of cases the antigen is recognized by the T cell receptor (TCR) as a complex of a foreign antigen and amino acid residues contributed by the major histocompatibility complex (MHC) antigens, and the antigen-specific, MHC-restricted effector function is an unambiguous result of this process. Alternatively, the T cell receptor may recognize a particular conformational form of the antigen which is dictated by the allelic differences in the MHC, resulting also in MHC-restricted recognition. When, however, a T cell which phenotypically fulfills all the requirements necessary to perform antigen specific, MHC-restricted function, shows a lack of MHC restriction, there are two possible explanations: 1) In addition to the MHC-restricted, antigen-specific T cell receptor the cell expresses, or has newly acquired the expression of another, MHC-unrestricted (NK-like) receptor, or 2) The specific antigen recognized by the T cell receptor, is able to bind to the receptor and activate the T cell without being presented by the MHC molecule. While the first possibility has been extensively described in the literature as well as other articles in this issue, the second possibility has not been dealt with to the same extent and is the primary focus of this review. 相似文献
88.
The pigment of substantia nigra human brain has been extracted by a mild procedure consisting of washes with phosphate buffer, methanol and incubation with SDS-proteinase. Pyrolisis gas chromatography mass spectrometry infrared spectrometry, termogravimetric analysis and elemental analysis were the techniques used for the chemical characterization. An indole moiety bound to a sulfur containing amino acid and to palmitic acid were the main aspects found in the structure. The presence of a 7% inorganic component was observed. This probably contains Fe, Cu, Zn and Cr which are also relevant, for the formation and the role of melanin in substantia nigra neurons. The fatty acid moiety is chemically bound to the indole structure as it was not eliminated by repeated methanol washing. The same situation occurs for the sulfur containing gropu. Considering these data and the most abundant molecules present in substantia nigra the precursor of neuromelanin seems to be a cysteinyl-cethecol, to which is then bound a palmityl group. 相似文献
89.
Claude Sauvage Jean-François Rumigny Michel Maitre 《Molecular and cellular biochemistry》1991,107(1):65-77
Summary Three G proteins from human brain membranes were purified to near homogeneity by conventional techniques including preparative
electrophoresis. These G proteins were characterized by their ability to bind GTP, GDP and GTP analogs. Two of these proteins
have molecular weights of 50,000 (G50) and 36,000 (G36), as determined on SDS-gels. G36 was ADP-ribosylated by pertussis toxin. Thus, G50 could represent a Gsα subunit, whereas G36 could be Giα or Goα. G50 was phosphorylated by cAMP dependent protein kinase and protein kinase C. G36 was phosphorylated by a protein kinase independent of calcium and phospholipid, a proteolytic product of protein kinase C,
analogous to protein kinase M. Phosphorylation of G36 by this protein kinase induced a dramatic decrease in its GTPase activity. The third G protein, of molecular weight 22,000
probably belongs to the group of monomeric G proteins possessing functional similarities withras gene products. The regulation of G proteins involving calcium-dependent and independent pathways is delineated. 相似文献
90.
N. Aste C. Viglietti-Panzica A. Fasolo C. Andreone H. Vaudry G. Pelletier G. C. Panzica 《Cell and tissue research》1991,265(2):219-230
Summary In the present study, we have demonstrated, by means of the biotin-avidin method, the widespread distribution of neuropeptide Y (NPY)-immunoreactive structures throughout the whole brain of the Japanese quail (Coturnix coturnix japonica). The prosencephalic region contained the highest concentration of both NPY-containing fibres and perikarya. Immunoreactive fibres were observed throughout, particularly within the paraolfactory lobe, the lateral septum, the nucleus taeniae, the preoptic area, the periventricular hypothalamic regions, the tuberal complex, and the ventrolateral thalamus. NPY-immunoreactive cells were represented by: a) small scattered perikarya in the telencephalic portion (i.e. archistriatal, neostriatal and hyperstriatal regions, hippocampus, piriform cortex); b) medium-sized cell bodies located around the nucleus rotundus, ventrolateral, and lateral anterior thalamic nuclei; c) small clustered cells within the periventricular and medial preoptic nuclei. The brainstem showed a less diffuse innervation, although a dense network of immunopositive fibres was observed within the optic tectum, the periaqueductal region, and the Edinger-Westphal, linearis caudalis and raphes nuclei. Two populations of large NPY-containing perikarya were detected: one located in the isthmic region, the other at the boundaries of the pons with the medulla. The wide distribution of NPY-immunoreactive structures within regions that have been demonstrated to play a role in the control of vegetative, endocrine and sensory activities suggests that, in birds, this neuropeptide is involved in the regulation of several aspects of cerebral functions.Abbreviations
AA
archistriatum anterius
-
AC
nucleus accumbens
-
AM
nucleus anterior medialis
-
APP
avian pancreatic polypeptide
-
CNS
centrai nervous system
-
CO
chiasma opticum
-
CP
commissura posterior
-
CPi
cortex piriformis
-
DIC
differential interferential contrast
-
DLAl
nucleus dorsolateralis anterior thalami, pars lateralis
-
DLAm
nucleus dorsolateralis anterior thalami, pars medialis
-
E
ectostriatum
-
EW
nucleus of Edinger-Westphal
-
FLM
fasciculus longitudinalis medialis
-
GCt
substantia grisea centralis
-
GLv
nucleus geniculatus lateralis, pars ventralis
-
HA
hyperstriatum accessorium
-
Hp
hippocampus
-
HPLC
high performance liquid chromatography
-
HV
hyperstriatum ventrale
-
IF
nucleus infundibularis
-
IO
nucleus isthmo-opticus
-
IP
nucleus interpeduncularis
-
IR
immunoreactive
-
LA
nucleus lateralis anterior thalami
-
LC
nucleus linearis caudalis
-
LFS
lamina frontalis superior
-
LH
lamina hyperstriatica
-
LHRH
luteinizing hormone-releasing hormone
-
LoC
locus coeruleus
-
LPO
lobus paraolfactorius
-
ME
eminentia mediana
-
N
neostriatum
-
NC
neostriatum caudale
-
NPY
neuropeptide Y
-
NIII
nervus oculomotorius
-
NV
nervus trigeminus
-
NVI
nervus facialis
-
NVIIIc
nervus octavus, pars cochlearis
-
nIV
nucleus nervi oculomotorii
-
nIX
nucleus nervi glossopharyngei
-
nBOR
nucleus opticus basalis (ectomamilaris)
-
nCPa
nucleus commissurae pallii
-
nST
nucleus striae terminalis
-
OM
tractus occipitomesencephalicus
-
OS
nucleus olivaris superior
-
PA
palaeostriatum augmentatum
-
PBS
phosphate-buffered saline
-
POA
nucleus praeopticus anterior
-
POM
nucleus praeopticus medialis
-
POP
nucleus praeopticus periventricularis
-
PP
pancreatic polypeptide
-
PYY
polypeptide YY
-
PVN
nucleus paraventricularis magnocellularis
-
PVO
organum paraventriculare
-
R
nucleus raphes
-
ROT
nucleus rotundus
-
RP
nucleus reticularis pontis caudalis
-
Rpc
nucleus reticularis parvocellularis
-
RPgc
nucleus reticularis pontis caudalis, pars gigantocellularis
-
RPO
nucleus reticularis pontis oralis
-
SCd
nucleus subcoeruleus dorsalis
-
SCv
nucleus subcoeruleus ventralis
-
SCNm
nucleus suprachiasmaticus, pars medialis
-
SCNl
nucleus suprachiasmaticus, pars lateralis
-
SL
nucleus septalis lateralis
-
SM
nucleus septalis medialis
-
Ta
nucleus tangentialis
-
TeO
tectum opticum
-
Tn
nucleus taeniae
-
TPc
nucleus tegmenti pedunculo-pontinus, pars compacta
-
TSM
tractus septo-mesencephalicus
-
TV
nueleus tegmenti ventralis
-
VeL
nucleus vestibularis lateralis
-
VLT
nucleus ventrolateralis thalami
-
VMN
nucleus ventromedialis hypothalami
A preliminary report of this study was presented at the 15th Conference of European Comparative Endocrinologists, Leuven, Belgium, September 1990 相似文献