{"title":"Differential responses of intracisternal injection of interleukin‐1 β to acute and inflammatory orofacial pain model in freely moving rats","authors":"H. Choi, J. S. Park, D. Ahn","doi":"10.1002/NRC.10047","DOIUrl":"https://doi.org/10.1002/NRC.10047","url":null,"abstract":"The present study was performed to investigate the modulatory role of certain interleukin (IL)-1β in nociception with a nociceptive jaw opening reflex and an orofacial formalin test in freely moving rats. In an acute pain model, 10 pg, 100 pg and 1 ng IL-1β injected intracisternally did not change the digastric eletromyogram (dEMG). However, 10 ng IL-1β suppressed dEMG to 76±8 % of control values. In an inflammatory pain model, 10 pg IL-1β injected intracisternally did not change formalin-induced noxious behavioral responses. However, 100 pg IL-1β increased formalin-induced noxious behavioral responses. At higher dose of 10 ng IL-1β, it did not increase formalin-induced behavioral responses. Pretreatment with IL-1 receptor antagonist abolished hyperalgesic response of 100 pg IL-1β. These results suggest that the intracisternal injection of IL-1β modulate the transmission of nociceptive information in the orofacial area. The hypo/hyper-algesic responses of central cytokines seem to depend on the pain model or dose related manner and the hyperalgesic action seems to be mediated by IL-1 receptor.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"43 1","pages":"145-154"},"PeriodicalIF":0.0,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80780023","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}
{"title":"Stimulation of Ca2+/Mg2+‐ATPase activity in adult rat cerebrocortical synaptosomes by 3‐5‐3′‐L‐triiodothyronine","authors":"Nilkanta Chakrabarti, A. Ray","doi":"10.1002/NRC.10052","DOIUrl":"https://doi.org/10.1002/NRC.10052","url":null,"abstract":"Stimulation of the calcium-stimulated and magnesium-dependent adenosine triphosphatase (Ca2+/Mg2+-ATPase) activity by 3-5-3′-L-triiodothyronine (T3) in synaptosomes prepared from adult rat cerebral cortex was demonstrated both in vitro and in vivo. T3 stimulated the Ca2+/Mg2+-ATPase activity in time dependent and dose dependent manner to depolarization-induced synaptosomes suspended in Ca2+-loaded choline-chloride buffer, represented involvement of the recovery phase of the changes in intrasynaptosomal Ca2+ level in this activation. T3 (100nM) also stimulated the enzyme activity in nondepolarized intact synaptosomes suspended in choline-chloride buffer. T3 had direct and dose-dependent stimulatory effect on the Ca2+/Mg2+-ATPase activity of the lysed synaptosomal suspension. The effect of T3 on the lysed synaptosomes was higher than that found on the nondepolarized intact synaptosomes. The condition probably represents the direct and/or indirect interaction of T3 with the enzyme through plasmamembrane related phenomenon that needs further investigation. After T3 treatment, a dose-dependent activation of the enzyme was found in vivo. It appears that T3 plays a role on adult brain neuronal Ca2+-mobilization through stimulation of the Ca2+/Mg2+-ATPase activity in nerve terminals.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"32 1","pages":"193-201"},"PeriodicalIF":0.0,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91352329","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}
T. Kurt, A. Oğuzhanoğlu, R. Ortaç, B. Turman, E. Adiguzel
{"title":"Effects of L‐arginine on the brain ischaemia‐reperfusion damage in rats: An investigation by somatosensory evoked potentials and histopathology","authors":"T. Kurt, A. Oğuzhanoğlu, R. Ortaç, B. Turman, E. Adiguzel","doi":"10.1002/NRC.10050","DOIUrl":"https://doi.org/10.1002/NRC.10050","url":null,"abstract":"We investigated whether administration of L-arginine reduces the ischaemia-reperfusion damage in the rat brain. The effects of L-arginine were evaluated by means of somatosensory evoked potential (SEP) measurements and quantitative histopathological investigations. There was no significant difference between groups based on SEP data. The results obtained from quantitative histopathological investigations indicate that the nitric oxide (NO) precursor L-arginine does not appear to have a protective effect on the brain ischaemia-reperfusion damage. Furthermore, histopathological evaluation revealed a higher number of damaged cells in the L-arginine treated rats than in control group. The results of the present study suggest that high concentrations of L-arginine present in later stages of reperfusion might have harmful effects on reperfusion damage in the brain.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"9 1","pages":"175-182"},"PeriodicalIF":0.0,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83429055","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}
{"title":"Effects of low‐dose scopolamine on locomotor activity: No dissociation between cognitive and non‐effects","authors":"G. Poorheidari, J. Pratt, Nima Dehghani","doi":"10.1002/NRC.10049","DOIUrl":"https://doi.org/10.1002/NRC.10049","url":null,"abstract":"Attempts have been made to dissociate the cognitive effects of scopolamine from its non-cognitive effects. It has been suggested that low doses of scopolamine may induce memory impairment without inducing significant non-cognitive effects. We therefore tested changes in locomotor activity (as a non-cognitive effect) in rats treated with low-dose scopolamine (which is believed to induce cognitive effects only). \u0000 \u0000 \u0000 \u0000In this study, locomotor activity (as a non-cognitive effect) induced by low doses of this drug was evaluated by using two methods and rat strains. In the first study (circular box method, an automated open-field), scopolamine hydrobromide (HBr), scopolamine methylbromide (MeBr) or saline was injected subcutaneously into male Sprague-Dawley rats. After 30 min, rats were put into an automated open-field and locomotor activity was quantified by recording interruptions of infrared beams, with print-outs every 2 min for 16 min. Locomotor activity was assessed by summing these recordings. In the second study (closed platform), scopolamine HBr or saline was injected intraperitoneally into male Long-Evans rats. Twenty minutes later, the rats were placed in the center of a square-shaped closed platform (with 3×3 divisions). Locomotor activity was defined as the sum of crossings (traversing of four paws of the rat from one area into another of nine) and rears, which were recorded every 5 min for 20 min. \u0000 \u0000 \u0000 \u0000Results from the circular box study showed that scopolamine HBr produced a marked increase in locomotor activity whereas scopolamine MeBr produced a non-significant decrease in locomotor activity. The closed platform data also demonstrated that scopolamine HBr increased locomotor activity significantly. \u0000 \u0000 \u0000 \u0000These data show that scopolamine can induce non-cognitive effects (such as increased locomotor activity), even at low doses. Our results also imply that the increase in locomotor activity is mediated centrally.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"37 4","pages":"165-174"},"PeriodicalIF":0.0,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91535637","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}
{"title":"Intrathecal methylprednisolone does not improve outcome after severe spinal cord injury in the rat","authors":"I. Vanický, L. Urdzikova, K. Saganová, M. Marsala","doi":"10.1002/NRC.10051","DOIUrl":"https://doi.org/10.1002/NRC.10051","url":null,"abstract":"In a rat model of spinal cord compression-induced injury, we have tested the hypothesis that intrathecally administered methylprednisolone will improve long-term recovery of the injured rats. The effect of the treatment was evaluated quantitatively as 1, behavioral testing of spontaneous locomotion and 2, morphometric measurement of the tissue loss in the white matter and grey matter, respectively. Intrathecal methylprednisolone elicited remarkable motor reactions in the paraplegic animals immediately after administration. However, during 4 weeks' survival, no significant differences were observed in the parameters of recovery between the methylprednisolone-treated and placebo-treated group. We conclude that intrathecal administration of methylprednisolone had no effect on the outcome after compressive spinal cord injury in the rat at the doses and timing used in the present study.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"26 1","pages":"183-191"},"PeriodicalIF":0.0,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83258136","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}
Yi Li, X. Yang, Jieli Chen, Lei Wang, Ying Wang, Chunling Zhang, Xiaoguang Chen, M. Katakowski, T. Mikkelsen, Mei Lu, M. Chopp
{"title":"Transplantation of a new composite of neural cells and marrow stromal cells into rat brain after stroke","authors":"Yi Li, X. Yang, Jieli Chen, Lei Wang, Ying Wang, Chunling Zhang, Xiaoguang Chen, M. Katakowski, T. Mikkelsen, Mei Lu, M. Chopp","doi":"10.1002/NRC.10048","DOIUrl":"https://doi.org/10.1002/NRC.10048","url":null,"abstract":"We constructed a biologic material composed of fetal rat brain cells (neurospheres) and adult rat bone marrow stromal cells (MSCs), designated as NMCspheres. Adult rats were subjected to 2 hours of middle cerebral artery occlusion (MCAo) and implanted with cultured prelabeled NMCspheres (n=6), neurospheres (n=5) or MSCs (n=6) into the ischemic penumbra at 24 hours after MCAo. Control adult rats (n=10) were subjected to MCAo alone. In vitro within the NMCspheres, MSCs rapidly formed a process network with intact neural cells compared with a necrotic core within neurospheres alone. An in vivo rat corneal assay demonstrated that NMCspheres enhanced angiogenesis compared to MSCs and neurospheres. Neurological functional recovery after stroke was enhanced in rats treated with NMCspheres, compared to rats with neurosphere or MSC treatments by day 7 and day 14 after transplantation. The NMCspheres are a new composite material that may be employed in the treatment of stroke.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"115 1","pages":"155-163"},"PeriodicalIF":0.0,"publicationDate":"2002-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79107877","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}
{"title":"Hindbrain glucoprivic inhibition of the proestrus lutenizing hormone surge in the female rat is attenuated by exogenous lactate administration","authors":"K. Briski","doi":"10.1002/NRC.10039","DOIUrl":"https://doi.org/10.1002/NRC.10039","url":null,"abstract":"Central glucose availability is a critical monitored variable in the regulation of reproductive neuroendocrine function. While current studies implicate the periventricular caudal brainstem as a source of signaling of decreased availability of catabolic intermediates and/or glycolytic end products, the mechanisms by which local metabolic ‘sensors’ signal diminished glucose utilization are not clear. The present experiments investigated whether fourth ventricular infusion of the aerobic catabolic substrate, lactate, attenuates glucoprivic suppression of luteinizing hormone (LH). Cyclic female rats were injected at 13.00h on proestrus with the glucose antimetabolite, 2-deoxy-D-glucose (2DG; 50 vs. 150ug), or vehicle into the rostral fourth ventricle. Additional proestrus animals were treated by continuous fourth ventricular infusion of 10.0 µM lactate/hr or vehicle, initiated prior to ip injection of 400mg 2DG/kg bw or saline. Serial blood samples were obtained hourly during proestrus afternoon for radioimmunoassay of plasma LH. The results demonstrate a reduction in the LH surge following icv 2DG administration, while showing that fourth ventricular infusion of lactate reversed inhibition of hormone release by systemic antimetabolite administration. These findings support the view that hindbrain signaling of glucose metabolic dysfunction initiates neural mechanisms that inhibit the proestrus LH surge, and that lactate utilization may be monitored as an indicator of local cellular energy stasis.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"10 1","pages":"67-73"},"PeriodicalIF":0.0,"publicationDate":"2002-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85943767","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}
L. Rodella, G. Bonaspetti, R. Rezzani, E. Borsani, R. Fenu, U. Pazzaglia, R. Bianchi
{"title":"Cyclosporine‐A delays the end‐plate degeneration in denerved rat muscles","authors":"L. Rodella, G. Bonaspetti, R. Rezzani, E. Borsani, R. Fenu, U. Pazzaglia, R. Bianchi","doi":"10.1002/NRC.10041","DOIUrl":"https://doi.org/10.1002/NRC.10041","url":null,"abstract":"When an adult skeletal muscle is denervated, its end-plates degenerate and their acethylcholinesterase (AChE) activity gradually decreases. However, if the proximal segment of the nerve is sutured to the distal segment, or if the nerve is implanted in a previous denerved muscle the axons regenerate and reconstitute new end-plates over a variable period. This period depends on the time passed between the nerve cutting and the reimplantation suggesting that the degenerative processes are closely correlated to regeneration. It has been shown that cyclosporine-A (CsA) is useful in nerve regeneration but their role in nerve degeneration is not well understand. We evaluated, using AChE histochemistry, the effects of CsA, on the degeneration of the end-plates in an experimental model of gastrocnemius muscle denervation in the rat. CsA at a dose of 15 mg/kg/day did not cause any quantitative or qualitative alterations in the end-plates on normal rat muscles. Moreover, our findings showed that CsA reduced the end-plate degeneration and loss in the denerved rat muscles.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"142 1","pages":"85-92"},"PeriodicalIF":0.0,"publicationDate":"2002-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88669140","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}
Keyue Ding, Xiaojing Sun, Min Zhou, Jing Cai, Tianjing Cai, Yan Zhang, Tongbin Zhu, Zhengguo Zhang, B. Qiang, Yan Shen
{"title":"Identification of novel protein-coding genes from human fetal hippocampus ESTs database","authors":"Keyue Ding, Xiaojing Sun, Min Zhou, Jing Cai, Tianjing Cai, Yan Zhang, Tongbin Zhu, Zhengguo Zhang, B. Qiang, Yan Shen","doi":"10.1002/NRC.10042","DOIUrl":"https://doi.org/10.1002/NRC.10042","url":null,"abstract":"We presented a procedure to identify novel protein-coding genes from human fetal hippocampus ESTs database generated in our previous study. The protocol is involved in searching the GenBank non-redundant (nr) protein database with ESTs coding regions query. We used ESTScan program to detect and reconstruct coding regions in the ESTs sequence data. With almost 10,000 raw ESTs analyzed, 4,061 coding regions were extracted. The corresponding amino acid sequences were then searched against the GenBank nr-protein databases; all the similarity hits were parsed in a homology analysis workbench. 22 ESTs were identified as the “seed” ESTs, which might be the fragment of the novel protein-coding genes. Indeed, further analysis of these ESTs in full-length cDNA cloning in silico, as well as the mapping information in UCSC and the added experimental proof, verified the effectiveness of the strategy. Taking advantage of rare ESTs resources, and the effective strategy, we would explore more novel genes in the human genome.\u0000 \u0000 \u0000 \u0000 [The ESTs sequence data described in this paper have been submitted to the GenBank data library (http://www.ncbi.nlm.nih.gov/dbEST) under accession nos. BM174886-958, BM259607-9; and the full length cDNA sequence can be obtained in http://www.chgb.org.cn/hippocampus.htm]","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"72 1","pages":"93-99"},"PeriodicalIF":0.0,"publicationDate":"2002-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87270389","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}
Ş. Şahin, S. Sogut, H. Ozyurt, E. Uz, A. Ilhan, O. Akyol
{"title":"Tissue xanthine oxidase activity and nitric oxide levels after spinal cord ischemia/reperfusion injury in rabbits: comparison of caffeic acid phenethyl ester (CAPE) and methylprednisolone","authors":"Ş. Şahin, S. Sogut, H. Ozyurt, E. Uz, A. Ilhan, O. Akyol","doi":"10.1002/NRC.10044","DOIUrl":"https://doi.org/10.1002/NRC.10044","url":null,"abstract":"Caffeic acid phenethyl ester exhibits antioxidant properties. This experimental study was designed to determine the effect of CAPE on nitric NO level and XO activity after reperfusion injury of spinal cord. New Zealand white rabbits were undergone aortic occlusion. CAPE, methylprednisolone or saline were injected intraperitoneally before surgical intervention. Animals were subjected to 21 min of crossclamp time. At the end of occlusion time, the clamps were removed and restoration of the blood flow was verified visually. Animals in sham group underwent a surgical procedure similar to the other groups but the aorta was not occluded. Spinal cord specimens were obtained to determine the tissue levels of NO and XO activity. \u0000 \u0000 \u0000 \u0000Both XO activity and NO level in ischemia group were significantly higher than those of sham group (p = 0.0005 and 0.0003, respectively). MP and CAPE had no effect on XO activity after reperfusion. These two agents decreased NO levels nearly to that of sham group after reperfusion. There were no differences between MP and CAPE on reducing NO level. These results suggest that rabbits with ischemia-reperfusion injury in spinal cord have increased cord concentrations of nitrite and nitrate that are indicative of endogenous overproduction of NO. CAPE may be regarded as an agent that protects spinal cord from ischemia-reperfusion injury.","PeriodicalId":19198,"journal":{"name":"Neuroscience Research Communications","volume":"42 1","pages":"111-121"},"PeriodicalIF":0.0,"publicationDate":"2002-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85114301","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}