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نویسندگان: 

PALIZVAN M.R. | GHAZNAVI RAD E.

اطلاعات دوره: 
  • سال: 

    2014
  • دوره: 

    9
  • شماره: 

    4
  • صفحات: 

    295-299
تعامل: 
  • استنادات: 

    1
  • بازدید: 

    343
  • دانلود: 

    0
چکیده: 

The role of opioid receptor and voltage dependent calcium channels on the kindling induced by the convulsant pentylenetetrazole (PTZ) were investigated in the rats. Experiment involved 24 rats which were divided into four groups. Kindling was established with PTZ in subconvulsive dose (37.5 mg/kg i.p.) every 48 h and effects were observed within 20 min using five-point scoring system. All animals were kindled to three consecutive-stage five seizures and their stability was tested. Saline, verapamil (calcium channel blocker), naloxone (opioid antagonist) or both of them were then administrated 20 min before PTZ application. Convulsant parameters were significantly (P<0.05) reduced by verapamil. Naloxone had no significant effect on the seizure expression of fully kindled animals, whereas simultaneous application of naloxone and verapamil had profound inhibitory effect on all seizure parameters. The results of the present study suggest that NALOXANE increased the inhibitory effect of verapamil on the seizure induced by PTZ kindling.

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اطلاعات دوره: 
  • سال: 

    2004
  • دوره: 

    3
  • شماره: 

    Supplement 2
  • صفحات: 

    42-43
تعامل: 
  • استنادات: 

    1
  • بازدید: 

    246
  • دانلود: 

    0
کلیدواژه: 
چکیده: 

The aqueous-ethanol extract of the Hypericum perforatum (Hp-Ext.) was studied for its possible effect on Naloxone (NLX)-precipitated Opium withdrawal physical signs in rats. Purified Opium was used to induce dependence in rats using 8 days treatment schedule. The animals received Opium extract orally twice daily at 09:00 hrs and 19:00 hrs starting with initial dose of 80 mg/kg (equivalent to 8 mg/kg morphine) and increasing to 650 mg/kg (equivalent to 65 mg/kg morphine). Withdrawal syndrome was precipitated with NLX (0.25 mg/kg, s/c). Animals were divided into three groups each containing nine rats. Group one served as a control and received opium + saline during opium dependence schedule and the remaining two groups were treatment group, one of which received Hp-Ext (20 mg/kg, p/o) one hour before NLX induced withdrawal and was administered opium + saline through out the dependence protocol and 2nd treated group received opium along with Hp-Ext doses though out the dependence protocol. The spasmolytic and calcium antagonist activities of the plant extract were studied using isolated tissue experiments suspended in the Krebs solution maintained at 37 ?C and aerated with carbogen gas. The results showed a significant decrease in both, NLX-induced Opium withdrawal Jumps and Wet Dog Shakes behavior in chronically treated group (ANOVA; P < 0.05 followed by Dunnet post hoc analysis) but no significant effect was found in the acute treatment group. Interestingly, a significant effect was observed on diarrhea in acute treatment group (ANOVA; p < 0.05, followed by Student Newman Keuls test) but no such effect was seen in the chronically treated group. In a separate study, the plant extract inhibited K+-induced contractions in isolated rabbit jejunum and trachea preparations thus showing spasmolytic effect mediated through calcium antagonist activity. In view of the reported fact that NLX-induced opioid withdrawal signs could be inhibited by calcium antagonists, our results indicate the possibility that the opioid withdrawal ameliorating effect of H. perforatum extract may be at least partly though calcium channel blockade. Acknowledgements: We gratefully acknowledge the help and cooperation for the supply of Opium by Anti Narcotic Force (ANF) Peshawar Division. Financial support of University of Pehsawar is also acknowledged.

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اطلاعات دوره: 
  • سال: 

    2016
  • دوره: 

    1
  • شماره: 

    2
  • صفحات: 

    9-16
تعامل: 
  • استنادات: 

    0
  • بازدید: 

    254
  • دانلود: 

    0
چکیده: 

The role of stress in the pathogenesis of ovarian cysts is believed to be mediated by the discharge of endogenous cortisol, which inhibits LH release. Endogenous opioid peptides are involved in many responses to stress. Therefore, the aim of this study was to determine the effect of epidural administration of Naloxone (NX) on cystic regression and follicle development leading to normal oestrus in dairy cattle. This study was conducted on 91 dairy cattle affected by follicular cysts, divided randomly into 3 groups.Group1 (n=30) cows were treated epidurally (lumbo-sacral) with 0.8 mg Naloxan hydrochloride (NX). Group2 (n=30) cows were treated epidurally with GnRH analogue (100 mcg gondorelin acetate). Group3 (n=31) cows were considered as control and received 5 ml normal saline epidurally. Although the results of this study showed that NALOXANE was better than the other two groups to treat follicular cysts, there was no significant difference in differnnt criteria, such as CL formation, increasing plasma P4 concentrations and 1st service conception rates among 3 groups.

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اطلاعات دوره: 
  • سال: 

    2004
  • دوره: 

    9
  • شماره: 

    1
  • صفحات: 

    26-33
تعامل: 
  • استنادات: 

    0
  • بازدید: 

    368
  • دانلود: 

    0
چکیده: 

Background: There is growing evidence indicating that neuronal calcium channels play an important role in the mechanism of Morphine dependence.Objective: To investigate the acute and long-term effects of Verapamil in Morphine dependent mice. Methods: Mice were rendered dependent on Morphine by subcutaneous injection of Morphine over a period of 5 days. The effects of acute and chronic administration of phenylalkylamine calcium channel antagonist, Verapamil, on Naloxone induced Morphine withdrawal signs was investigated.Results: A single injection of Verapamil proved to be effective in inhibiting some signs of Morphine withdrawal but ineffective in changing the number of jumps. The concurrent injections of Verapamil with Morphine prevented most signs of Morphine withdrawal.Conclusion: The results confirmed the crucial role of voltage-sensitive calcium channels in the adaptations that occur after long-term treatment with Morphine. Concurrent injections of Verapamil with Morphine could be used to prevent some signs of Morphine withdrawal.

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نویسنده: 

ZAREI LEILA | Farhad Negin | ABTAHI FROUSHANI SEYYED MEYSAM | ESMAEILI GOUVARCHIN GHALEH HADI | MANSOURI MOTLAGH BAHMAN

اطلاعات دوره: 
  • سال: 

    2015
  • دوره: 

    1
تعامل: 
  • بازدید: 

    155
  • دانلود: 

    0
چکیده: 

OBJECTIVE: MESENCHYMAL STEM CELLS (MSCS) IN BONE MARROW FORM A NICHE THAT HAS INEVITABLE INTERACTIONS WITH MACROPHAGE. MOREOVER, PREVIOUS DOCUMENTS HAVE SHOWN THAT NALOXANE HAS AN IMPORTANT ROLE IN REGULATING THE CELL GROWTH OF MSCS.

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اطلاعات دوره: 
  • سال: 

    2012
  • دوره: 

    13
  • شماره: 

    3 (52)
  • صفحات: 

    138-142
تعامل: 
  • استنادات: 

    0
  • بازدید: 

    283
  • دانلود: 

    0
چکیده: 

Background: Punica granatum Linn. (PG) is native to the Mediterranean region. Its flower exhibited antioxidant activity. The present study attempt to investigate the effect of these extract on uterine contraction and its possible mechanism (s).Methods: Thirty five female Wistar rats (200-300 g) at estrous phases of cycle was examined in this study, pieces of virgin adult rat uterus (1.5cm) were suspended in an organ bath containing 10ml of De Jalon solution at 29oC. Tissue contractility was isometric ally recorded. KCl (60mM), BaCl2 (4 mM) and oxytocin (10 mU/ml) were applied to the tissue in the presence and absence of aqueous and hydroalcoholic extracts of the plant (0.05, 0.1, 0.2, 0.4 and 0.8 mg/ml). Propranolol (1 mM) and NALOXANE (1mM) were added in KCl induced contractions. The results were analyzed by ANOVA and p<0.05 were considered as significant.Results: Cumulative concentration of extracts reduced uterine contractions induced by KCl dose-dependently (p<0.01). Extracts in a dose dependent (p<0.05) reduced uterine contractions decreased dose-dependently after of addition oxytocin. The extracts added cumulatively to the organ bath reduced contractions but they did not affect uterine contractions induced by BaCl2 except the last dose. Spasmolytic effects of the extracts were not affected by propranolol or NALOXANE in KCl induced contractions.Conclusion: Extracts diminished K+-induced contraction in uterus, therefore it seems that substances that decrease K+-induced contraction can also block voltage dependent calcium channel. The extracts did not have any effect on b-adrenoceptors or potassium channels.

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اطلاعات دوره: 
  • سال: 

    2009
  • دوره: 

    19
تعامل: 
  • بازدید: 

    183
  • دانلود: 

    0
چکیده: 

In this study the effect of hydroalcoholic extract of Ziziphora tenuior (Z.t.) on visceral pain and involvement of opioidergic and serotoninergic systems were investigated. For this purpose from male mice (28±3g) were used. Animals were grouped randomly in to control, positive control and receivers of Ziziphora tenuior extract. Control group and positive control group received normal saline 0.9% and indomethacin (5mg/kg, i.p.), respectively. Treatments groups were injected with doses, (50mg/kg, i.p.), (75mg/kg, i.p.) and (100 mg/kg, i.p.) of hydroalcoholic extract of Ziziphora tenuior. Animals were injected with acetic acid 0.6% (10ml/kg) for iducing of visceral pain, 30 minutes after of each intraperitoneal administration. Antinociceptive effect was recorded by counting the number of writhes immediately after injection of acetic acid during 30 minutes. The potent dose of extract was used in following treatments. Involvement of opioidergic and serotoninergic systems in the antinociceptive effects of Z.t. extract were studied with pretreatment of opioid antagonist, NALOXANE (2mg/kg, i.p.) and serotoninergic antagonist, cyproheptadine (4mg/kg, i.p.) 15 minute before the administration of the extract in writhing test. The results of this study showed that hydroalcoholic extract of Ziziphora tenuior with doses (50mg/kg), (75mg/kg) and (100mg/kg) in a dose dependent manner and indomethacin (5mg/kg) induced significant reduction in pain response when compared to control group (P<0.05). Pretreatment with NALOXANE and cyproheptadine increased the pain sensation compared to the control (P<0.05) that confirms the involvement of opioidergic and serotoninergic systems in the extract induced antinociceptive effects.

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اطلاعات دوره: 
  • سال: 

    1389
  • دوره: 

    65
  • شماره: 

    1
  • صفحات: 

    57-60
تعامل: 
  • استنادات: 

    0
  • بازدید: 

    1490
  • دانلود: 

    253
چکیده: 

کاکوتی گیاهی متعلق به خانواده نعنا عیان است که به وفور در ایران یافت می شود. این گیاه در طب سنتی ایران به عنوان ضد درد و برای درمان بیماری های گوارشی استفاده می شود.این مطالعه به منظور بررسی اثرات ضد دردی عصاره هیدروالکلی گیاه کاکوتی بر درد احشایی و مداخله احتمالی آن با سیستم های اپیوئیدرژیک و سروتونرژیک، در موش های سوری نر نژاد N-MRI انجام گرفت. در این مطالعه اثر ضد دردی گیاه کاکوتی با استفاده از تست رایتینگ به عنوان یک مدل درد احشایی بررسی شد. بدین منظور، عصاره گیاه کاکوتی با دوزهای 50، 75 و 100 میلیگرم بر کیلوگرم به صورت داخل صفاقی تجویز و اثرات ضد دردی آن با ایندومتاسین (5mg/kg,i.p.) و گروه کنترل مقایسه گردید. سپس موثرترین دوز عصاره برای آزمایشات بعدی انتخاب شد و مداخله سیستم های اپیوئیدی و سروتونینی بر اثرات بی دردی ناشی از عصاره به ترتیب با استفاده از پیش درمانی با آنتاگونیست اپیوئیدی، نالوکسان (2mg/kg,i.p.) و آنتاگونیست سروتونرژیک، سیپروهپتادین (4mg/kg,i.p.)، 15 دقیقه قبل از تجویز عصاره به روش رایتینگ مورد بررسی قرار گرفت. نتایج این تحقیق نشان داد که عصاره هیدرو الکلی گیاه کاکوتی با دوزهای 50، 75 و 100 میلیگرم بر کیلوگرم و ایندومتاسین (5mg/kg) کاهش معنی داری را در پاسخ به درد در مقایسه با گروه کنترل ایجاد می کند (p<0.05) در حالی که پیش درمانی با نالوکسان و سیپروهپتادین بخشی از اثرات ضد دردی ناشی از عصاره را در مقایسه با گروه کنترل مهار کرد (p<0.05) این مطالعه نشان داد که بخشی از خصوصیات ضد دردی گیاه کاکوتی بوسیله مکانیسم های اپیوئیدرژیک و سروتونرژیک میانجی گری می شود که استفاده های مرسوم از گیاه را در درمان درد تایید می کند.

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نویسندگان: 

جاویدان نژاد عبداله

اطلاعات دوره: 
  • سال: 

    0
  • دوره: 

    8
  • شماره: 

    26
  • صفحات: 

    65-74
تعامل: 
  • استنادات: 

    0
  • بازدید: 

    1063
  • دانلود: 

    0
کلیدواژه: 
چکیده: 

 تجربه دانشمندان ثابت نموده که مواد شبه مورفین در مغز، اثرات مختلفی همچون مورفین داشته و با نالوکسان (NALOXANE) اثرشان از بین می رود.این مواد که Enkephline نامیده می شوند پروتئین هستند و از نظر ساختمانی شیمیایی از پنج اسید آمینه تشکیل شده اند.تابحال دو نوع Enkephline کشف شده است که این دو در چهار اسید آمینه مشترک بوده و پنجمین اسد آمینه در یکی میتونی Mitonine و در دیگری لوسین Leusin می باشد.

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اطلاعات دوره: 
  • سال: 

    1387
  • دوره: 

    10
  • شماره: 

    2 (مسلسل 38)
  • صفحات: 

    61-68
تعامل: 
  • استنادات: 

    0
  • بازدید: 

    1059
  • دانلود: 

    236
چکیده: 

هدف: در پژوهش حاضر، اثر تزریق درون هیپوکامپی هیستامین به صورت دو طرفه بر رفتارهای شبه اضطرابی در موش های صحرایی حساس شده به مورفین بررسی شد.روش: ابتدا با تزریق مورفین به مدت سه روز و سپس دوره پنج روزه بدون دارو حساسیت ایجاد شد، و سپس با استفاده از ماز به علاوه ای شکل (+) حیوانات آزمایش شدند.یافته ها: تزریق درون هیپوکامپی هیستامین درصد زمان طی شده در بازوی باز و تعداد ورود به بازوی باز را کاهش داد، اما بر فعالیت حرکتی تاثیری نداشت که این اثر اضطراب زایی هیستامین را نشان می دهد. اما تزریق هیستامین در حیوان حساس شده به مورفین، در مقایسه با گروه هایی که سالین دریافت کرده بودند، درصد زمان طی شده در بازوی باز و تعداد ورود به بازوی باز را افزایش داد که نشان دهنده کاهش اضطراب حیوان حساس شده است.نتیجه گیری: تزریق دو طرفه هیستامین در ناحیه هیپوکامپ شکمی، اثر اضطراب زایی بر جای می گذارد که این اضطراب ناشی از تزریق هیستامین در موش های حساس شده با مورفین کاهش می یابد. نالوکسان آثار مورفین را بر اضطراب زدایی آنتاگونیزه می کند.

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