Biological signals and receptors最新文献

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Changes in phospholipids and free fatty acids in the brains of mice preconditioned by hypoxia. 缺氧预处理小鼠大脑中磷脂和游离脂肪酸的变化。
Biological signals and receptors Pub Date : 1999-07-01 DOI: 10.1159/000014596
C Duan, F Yan, G Lu, H Liu, N Yin
{"title":"Changes in phospholipids and free fatty acids in the brains of mice preconditioned by hypoxia.","authors":"C Duan,&nbsp;F Yan,&nbsp;G Lu,&nbsp;H Liu,&nbsp;N Yin","doi":"10.1159/000014596","DOIUrl":"https://doi.org/10.1159/000014596","url":null,"abstract":"<p><p>Changes in the composition and contents of phospholipids and free fatty acids were observed and compared in three groups: (A) unpreconditoned normal controls, (B) exposure to 1 run of hypoxia and (C) exposure to 4 runs of hypoxia. In group B, the content of phosphatidyl ethanolamine (PE), phosphatidyl serine (PS) and free fatty acids (FFAs) increased significantly and the content of phosphatidyl choline (PC) and sphingomyelin (SM) decreased significantly. While in group C the content of PE, PS, PC and FFAs changed significantly when compared with that of group B, all phospholipid (except SM) and FFA contents tended to decrease to the level of group A. No new FFA was seen in the brain homogenates in any of the three groups. These results suggest that the changes in the content of mouse brain phospholipids and FFAs may be adaptive and involved in the animals' tolerance to hypoxia.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 4-5","pages":"261-6"},"PeriodicalIF":0.0,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014596","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21356725","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Changes of superoxide dismutase, glutathione perioxidase and lipid peroxides in the brain of mice preconditioned by hypoxia. 缺氧预处理小鼠脑内超氧化物歧化酶、谷胱甘肽周期氧化酶及脂质过氧化物的变化。
Biological signals and receptors Pub Date : 1999-07-01 DOI: 10.1159/000014595
C Duan, F Yan, X Song, G W Lu
{"title":"Changes of superoxide dismutase, glutathione perioxidase and lipid peroxides in the brain of mice preconditioned by hypoxia.","authors":"C Duan,&nbsp;F Yan,&nbsp;X Song,&nbsp;G W Lu","doi":"10.1159/000014595","DOIUrl":"https://doi.org/10.1159/000014595","url":null,"abstract":"<p><p>We have developed an animal model of hypoxic preconditioning and assumed that oxygen radicals and their endogenous scavenging enzymes may play an important role in the preconditioning. To test this hypothesis, activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and the content of lipid peroxides (LPO) were measured during the preconditioning. Compared with unpreconditioned control animals, in animals exposed to hypoxia only once, the activities of SOD and GSH-Px in whole brain were found to be significantly decreased while the LPO content in the hippocampus significantly increased. However, those in animals exposed to 4 runs of hypoxia tended to return to control levels and were lower than those in animals exposed to 1 and 2 runs of hypoxia. Our results indicate that the oxygen radicals and their specific scavenging enzymes seem to be involved in the development of tolerance to hypoxia.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 4-5","pages":"256-60"},"PeriodicalIF":0.0,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014595","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21356811","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 34
Hypoxia-ischemia-induced apoptotic cell death correlates with IGF-I mRNA decrease in neonatal rat brain. 缺氧缺血诱导的凋亡细胞死亡与新生大鼠脑IGF-I mRNA下降相关。
Biological signals and receptors Pub Date : 1999-07-01 DOI: 10.1159/000014599
T F Clawson, S J Vannucci, G M Wang, L B Seaman, X L Yang, W H Lee
{"title":"Hypoxia-ischemia-induced apoptotic cell death correlates with IGF-I mRNA decrease in neonatal rat brain.","authors":"T F Clawson,&nbsp;S J Vannucci,&nbsp;G M Wang,&nbsp;L B Seaman,&nbsp;X L Yang,&nbsp;W H Lee","doi":"10.1159/000014599","DOIUrl":"https://doi.org/10.1159/000014599","url":null,"abstract":"<p><p>Hypoxia-ischemia induces apoptotic and necrotic cell death, which results partially from persistent alterations in cellular energy homeostasis. Insulin-like growth factor I (IGF-I) is an anabolic pleiotrophic factor required by developing neurons for their optimal proliferation, differentiation, and survival. To determine how cell death and changes in IGF-I gene expression relate to the extent of hypoxia-ischemia, we evaluated the time course of apoptosis in a neonatal hypoxia-ischemia model in relation to the cellular distribution of IGF-I and IGFBP5 mRNA. Severe hypoxia-ischemia results in an immediate decrease in neuronal IGF-I and IGFBP5 mRNA. The decrease in neuronal IGF-I mRNA was concurrent with an increase in the number of apoptotic cells. It is conceivable that the immediate decrease in IGF-I gene expression may contribute to the impending neuronal death and selective vulnerability of myelinogenesis during the perinatal period.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 4-5","pages":"281-93"},"PeriodicalIF":0.0,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014599","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21356727","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 49
Neurophysiological changes associated with selective neuronal damage in hippocampus following transient forebrain ischemia. 短暂性前脑缺血后海马选择性神经元损伤的神经生理变化。
Biological signals and receptors Pub Date : 1999-07-01 DOI: 10.1159/000014600
Z C Xu, T M Gao, Y Ren
{"title":"Neurophysiological changes associated with selective neuronal damage in hippocampus following transient forebrain ischemia.","authors":"Z C Xu,&nbsp;T M Gao,&nbsp;Y Ren","doi":"10.1159/000014600","DOIUrl":"https://doi.org/10.1159/000014600","url":null,"abstract":"<p><p>Neurophysiological changes of hippocampal neurons were compared before and after transient forebrain ischemia using intracellular recording and staining techniques in vivo. Ischemic depolarization (ID) was used as an indication of severe ischemia. Under halothane anesthesia, approximately 13 min of ID consistently produced severe neuronal damage in the CA1 region of rat hippocampus, while CA3 pyramidal neurons and dentate granule cells remained intact. After such severe ischemia, approximately 60% of the CA1 neurons exhibited a synaptic potentiation. The excitability of these neurons progressively decreased following reperfusion. Approximately 30% of the CA1 neurons showed a synaptic depression following ischemia. The excitability of these neurons transiently decreased following reperfusion. After ischemia of the same severity, both synaptic transmission and excitability of CA3 and granule cells transiently depressed. These data suggest that ischemia-induced synaptic potentiation may be associated with the pathogenesis of neuronal damage following ischemia, and that the synaptic depression may have protective effects on hippocampal neurons after ischemic insult.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 4-5","pages":"294-308"},"PeriodicalIF":0.0,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014600","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21356730","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 33
Acute adaptation of mice to hypoxic hypoxia. 小鼠对缺氧的急性适应。
Biological signals and receptors Pub Date : 1999-07-01 DOI: 10.1159/000014594
G Lu, D Ding, M Shi
{"title":"Acute adaptation of mice to hypoxic hypoxia.","authors":"G Lu,&nbsp;D Ding,&nbsp;M Shi","doi":"10.1159/000014594","DOIUrl":"https://doi.org/10.1159/000014594","url":null,"abstract":"<p><p>Tolerance to hypoxia in vivo and in vitro was significantly increased by acute and repetitive exposure of mice to autoprogressive hypoxia. The average tolerance times of the successive 2nd, 3rd, 4th and 5th runs of exposure were, respectively, 2, 4, 6 and 8 times as long as that of the first exposure. The survival times under hypobaric chamber and cyanide toxification in the 4th exposure were, respectively, 10 (and even as much as 86) and 4 times those in control mice without exposure to hypoxia. Mandibular respiration and spinal reflex in vitro in hypoxia-resistant animals lasted 5-6 times as long as in control animals not previously exposed to hypoxia. Animals that received brain homogenate from hypoxia-resistant mice remained alive in a hypobaric chamber 2 times as long as those that received homogenate from controls and those that received saline. These results indicate that a kind of quickly developing adaptation with increased tolerance is achieved by acute and repetitive exposure of mice to progressive autohypoxia and some plastic or adaptive changes occur in the brain of hypoxia-resistant animals, including the production of some kind of water-soluble antihypoxic factors.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 4-5","pages":"247-55"},"PeriodicalIF":0.0,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014594","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21356812","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 23
Role of excitatory amino acids in hypoxic preconditioning. 兴奋性氨基酸在缺氧预处理中的作用。
Biological signals and receptors Pub Date : 1999-07-01 DOI: 10.1159/000014597
J Xie, G Lu, Y Hou
{"title":"Role of excitatory amino acids in hypoxic preconditioning.","authors":"J Xie,&nbsp;G Lu,&nbsp;Y Hou","doi":"10.1159/000014597","DOIUrl":"https://doi.org/10.1159/000014597","url":null,"abstract":"<p><p>We examined the effects of the extrinsic ionotropic NMDA receptor agonist (aspartate) and antagonist (ketamine) on the hypoxic preconditioning of mice and the concentration changes of intrinsic excitatory amino acids (EAAs), aspartate and glutamate, in the whole brain and different brain regions during preconditioning by an HPLC method. Our results showed that aspartate and ketamine significantly prolonged and shortened the standard tolerance time of mice during preconditioning and survival time in hypobaric chambers, respectively. After the 1st exposure, EAA concentrations in the whole brain and brain regions were increased. After run 4, they were decreased or maintained. It is suggested that the activation and suppression of ionotropic NMDA receptors is harmful and beneficial to hypoxic preconditioning, respectively. Degradation and/or inactivation of EAAs might be beneficial to the tolerance of mice to hypoxia.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 4-5","pages":"267-74"},"PeriodicalIF":0.0,"publicationDate":"1999-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014597","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21356729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 25
Regulation of the plasminogen activator system in the ovary. 卵巢纤溶酶原激活剂系统的调节。
Biological signals and receptors Pub Date : 1999-05-01 DOI: 10.1159/000014587
Y X Liu
{"title":"Regulation of the plasminogen activator system in the ovary.","authors":"Y X Liu","doi":"10.1159/000014587","DOIUrl":"https://doi.org/10.1159/000014587","url":null,"abstract":"<p><p>Extracellular matrix (ECM) not only provides a structural support for the organism, but also actively conducts cell-to-cell signal transduction and regulates cell proliferation, migration, development and metabolism. The targeted ECM degradation generated by plasminogen activator (PA) and regulated by plasminogen activator inhibitor (PAI) is, therefore, an event that affects a wide variety of physiological and pathological processes. The ovary is the best model to study the regulation and function of extracellular proteolysis mediated by multicomponents like the PA system. Studies carried out over the past 10 years in a number of laboratories have elucidated some of the biochemical events related to the function and regulation of the PA system in the ovary: hormone-induced proteolytic activity provided by tissue-type PA(tPA) and modulated by PAI-1 in the preovulatory follicles is responsible for a controlled and directed proteolysis leading to rupture of selected follicles during ovulation, whereas the coordinated expression of urokinase-type PA (uPA) and PAI-1 in the early growing follicle may be important in ECM degradation during cell proliferation and migration; the PA system may also play a role in the control of corpus luteum (CL) development through an autocrine or paracrine mechanism. Increase in tPA and PAI-1 expression in CL at a later stage is well correlated with a sharp decrease in CL progesterone production, while the increase in uPA mRNA levels and activity in the early stage of CL development is correlated with an increase in progesterone secretion.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 3","pages":"160-77"},"PeriodicalIF":0.0,"publicationDate":"1999-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014587","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21084577","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 33
Twenty-four hour rhythms of hypothalamic corticotropin-releasing hormone, thyrotropin-releasing hormone, growth hormone-releasing hormone and somatostatin in rats injected with Freund's adjuvant. 注射弗氏佐剂大鼠下丘脑促肾上腺皮质激素释放激素、促甲状腺激素释放激素、生长激素释放激素和生长抑素的24小时节律。
Biological signals and receptors Pub Date : 1999-05-01 DOI: 10.1159/000014588
A I Esquifino, L Selgas, E Vara, A Arce, D P Cardinali
{"title":"Twenty-four hour rhythms of hypothalamic corticotropin-releasing hormone, thyrotropin-releasing hormone, growth hormone-releasing hormone and somatostatin in rats injected with Freund's adjuvant.","authors":"A I Esquifino,&nbsp;L Selgas,&nbsp;E Vara,&nbsp;A Arce,&nbsp;D P Cardinali","doi":"10.1159/000014588","DOIUrl":"https://doi.org/10.1159/000014588","url":null,"abstract":"<p><p>The effect of Freund's adjuvant injection on 24-hour variation of hypothalamic corticotropin-releasing hormone (CRH), thyrotropin-releasing hormone (TRH), GH-releasing hormone (GRH) and somatostatin levels was examined in adult rats kept under light between 0800 and 2000 h daily. Groups of rats receiving Freund's complete adjuvant or its vehicle 3 days before sacrifice were killed at six different time intervals throughout a 24-hour cycle. In the median eminence, adjuvant vehicle-injected rats exhibited significant 24-hour variations for the four hormones examined, with maxima at noon. These 24-hour rhythms were inhibited or suppressed by Freund's adjuvant injection. In the anterior hypothalamus of adjuvant vehicle-treated rats, CRH content peaked at 1600 h, while two peaks were found for TRH and GRH levels, i.e., at 2400-0400 h and 1600 h. Freund's adjuvant injection suppressed 24-hour rhythm of anterior hypothalamic CRH, TRH and GRH content and uncovered a peak in anterior hypothalamic somatostatin levels at 0400 h. In the medial hypothalamus of adjuvant vehicle-treated rats, significant 24-hour variations were detectable for TRH (peaks at 1600 and 2400 h) and somatostatin (peak at 2400 h) which disappeared after Freund's adjuvant injection. In the posterior hypothalamus of adjuvant vehicle-treated rats, two peaks were apparent for CRH, TRH and somatostatin levels, i.e. at 1600 h and 2400-0400 h, this hormonal profile remaining unmodified after Freund's adjuvant administration. The administration of the immunosuppressant drug cyclosporine (5 mg/kg, 5 days) impaired the depressing effect of Freund's adjuvant injection on CRH, TRH and somatostatin content in median eminence, but not that on GRH. In the anterior hypothalamus, cyclosporine generally prevented the effect of immunization on hormone levels an revealed a second maximum in TRH at 0400 h. Cyclosporine also restored 24-hour variations in TRH and somatostatin levels of medial hypothalamus of Freund's adjuvant-injected rats but was unable to modify them in the posterior hypothalamus. The results further support the existence of a significant effect of immune-mediated inflammatory response at an early phase after Freund's adjuvant injection on hypothalamic levels which was partially sensitive to immunosuppression by cyclosporine.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 3","pages":"178-90"},"PeriodicalIF":0.0,"publicationDate":"1999-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014588","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21084580","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
Neurotransmitters and neuropeptides in the developing human central nervous system. A review. 发育中的人类中枢神经系统中的神经递质和神经肽。复习一下。
Biological signals and receptors Pub Date : 1999-05-01 DOI: 10.1159/000014586
D T Yew, W Y Chan, C B Luo, D R Zheng, M C Yu
{"title":"Neurotransmitters and neuropeptides in the developing human central nervous system. A review.","authors":"D T Yew,&nbsp;W Y Chan,&nbsp;C B Luo,&nbsp;D R Zheng,&nbsp;M C Yu","doi":"10.1159/000014586","DOIUrl":"https://doi.org/10.1159/000014586","url":null,"abstract":"<p><p>This is a review on the ontogenesis of major neurotransmitters and neuropeptides in the developing human central nervous system. In general, the molecules under study appeared early in development, usually in the first trimester. Cholinergic neurons were found to be present around the time of neuropeptide formation. The newly formed neuropeptidergic fibers extended towards the cholinergic centers where both might interact. In the major centers of the central nervous system, neuropeptides were also noted to colocalize with various neurotransmitters. For example, in the facial nucleus, enkepahlin and substance P fibers coexisted with cholinergic and catecholaminergic neurons, suggesting complex interactions. In the interpeduncular nucleus, peptidergic neurons acting as interneurons clearly modulated the afferent input to this nucleus. In the hippocampus and in sensory organs such as the retina, there were indications that neuropeptides and gamma-amino butyric acid coexisted. We hypothesize that interactions of neurotransmitters and peptides in neurons and fibers early in development play an indispensable role in the morphogenesis of the human central nervous system.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 3","pages":"149-59"},"PeriodicalIF":0.0,"publicationDate":"1999-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014586","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21084675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
Indole melatonin agonists and antagonists derived by shifting the melatonin side chain from the C-3 to the N-1 or to the C-2 indole position. 吲哚褪黑激素激动剂和拮抗剂是通过将褪黑激素侧链从吲哚的C-3位转移到N-1位或C-2位而获得的。
Biological signals and receptors Pub Date : 1999-01-01 DOI: 10.1159/000014565
G Tarzia, G Diamantini, G Spadoni
{"title":"Indole melatonin agonists and antagonists derived by shifting the melatonin side chain from the C-3 to the N-1 or to the C-2 indole position.","authors":"G Tarzia,&nbsp;G Diamantini,&nbsp;G Spadoni","doi":"10.1159/000014565","DOIUrl":"https://doi.org/10.1159/000014565","url":null,"abstract":"<p><p>This article reviews our efforts in the development of indole melatonin (MLT) agonist and antagonist compounds. Evidence is presented which indicates that high-affinity melatonergic agonists were obtained by shifting the MLT amido side chain from the C-3 to the N-1 indole position. Conversely, by moving the side chain from the C-3 to the C-2 indole position it is possible to produce MLT antagonist compounds.</p>","PeriodicalId":79565,"journal":{"name":"Biological signals and receptors","volume":"8 1-2","pages":"24-31"},"PeriodicalIF":0.0,"publicationDate":"1999-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000014565","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"20957926","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
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