scholarly journals A dizájner drog metiléndioxi-pirovaleron hatása a fejlődő idegrendszerre kísérletes állatmodellben

2015 ◽  
Vol 156 (30) ◽  
pp. 1221-1225
Author(s):  
László István Gerecsei ◽  
Ágota Ádám
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Locomotor Activity ◽  
Grip Strength ◽  
Open Field ◽  
Field Test ◽  
Motor Coordination ◽  
Open Field Test ◽  
Strength Test ◽  
Maternal Behaviour

Introduction: The designer drug methylenedioxypyrovalerone is a frequently used psychoactive drug of abuse. Aim: The aim of this study was to determine the effect of methylenedioxypyrovalerone, administrated from the 8th to the 14th day of the gestation, on the development of central nervous system and on the behaviour of offspring mice. Method: Pregnant mice were treated during this period either with subcutaneous injection of 1×10 mg/kg body weight methylenedioxypyrovalerone or vehicle (saline). Maternal behaviour (pup retrieval test), locomotor activity (open field test) and motor coordination (grip strength test) of dams were evaluated. Locomotor activity at the 7th and 21st postnatal day (open field test) and motor coordination at the 21st postnatal day (grip strength test) were examined. Results: Reduced maternal behaviour among treated animals was observed. There was no difference in the results of the open field test between treated and control groups. Decrease of locomotor activity was observed in the pups of the methylenedioxypyrovalerone treated dams. Conclusions: The results suggest that cathinones (in particular methylenedioxypyrovalerone) may adversely affect neural integrity of the developing central nervous system. Orv. Hetil., 2015, 156(30), 1221–1225.

The effect of Qing Huan Ling combined risperidone on the open field behavior of schizophrenic mice model

2016 ◽  
Vol 33 (S1) ◽  
pp. s289-s289
Author(s):  
Y. Zhang ◽  
F. Liu ◽  
Z. Dai ◽  
B. Wu ◽  
Q. Wu
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Locomotor Activity ◽  
Open Field ◽  
Open Field Test ◽  
Model Group ◽  
Mice Model ◽  
Blank Group ◽  
The Central Nervous System ◽  
Risperidone Group

ObjectiveTo observe the effect of Qing Huan Ling and (or) risperidone on locomotor activity and explorative behavior of schizophrenia mice model by open field test.MethodsSeventy kunming mice were randomly divided into 5 groups, one group as blank group. The rest groups ip MK-801 continuously 14 day, then randomly numbered: model group, risperidone group, Qing Huan Ling group and risperidone combined Qing Huan Ling group. Ig give corresponding drugs for each group 4 weeks, observe the change of locomotor activity and explorative behavior by open field test.ResultsAfter Ig 4 weeks, compared with the blank group, there were no obvious difference in locomotor activity and explorative behavior between risperidone group, Qing Huan Ling group and the combined group. Compared with the model group, risperidone had statistics meaning in the repression of explorative behavior (P < 0.05),the combined group has statistics meaning in the repression of locomotor activity and explorative behavior (78.92 ± 36.18 m vs. 186.92 ± 41.08 m, P < 0.01).ConclusionQing Huan Ling regulate the central nervous system of schizophrenia mice model; when combined with risperidone, it restrain the central nervous system of schizophrenia mice model and the effect is stronger than risperidone alone.Disclosure of interestThe authors have not supplied their declaration of competing interest.

scholarly journals Proposal of open field test as a model of varenicline pharmacokinetic study in rats

2018 ◽  
Vol 11 (3) ◽  
Author(s):  
Julia Zaccarelli-Magalhães ◽  
Thaisa Meira Sandini ◽  
André Rinaldi Fukushima ◽  
Helenice De Souza Spinosa
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Single Dose ◽  
Open Field ◽  
Field Test ◽  
Open Field Test ◽  
Male Rats ◽  
Control Group ◽  
Immobility Time ◽  
The Central Nervous System

Varenicline is a medication used for smoking treatment that acts as a partial agonist for nicotinic cholinergic receptors α4β2 and α3β4 and as a total agonist of receptor α7 in the central nervous system. Pharmacokinetic is important information for medications that acts in the central nervous system. This kind of assay is commonly done by expensive and complex analytical techniques. Therefore, the aim of this study was to evaluate the possibility of using the open field test as a pharmacokinetic model for varenicline in male rats exposed to a single dose of varenicline. Male rats received a single dose orally (gavage) of three different concentrations of varenicline: 0.03 (therapeutic dose for humans), 0.1 and 0.3 mg/kg or water (control group). The open field observations were recorded 30 min, 1, 2, 4, 6, 24, 48, 72 h and 7 days after the administration of varenicline or water. The results showed alterations in locomotion and rearing frequencies, as well as in immobility time observed in open field, which is consistent with this drug’s plasma peak. Consequently, this behavioral test apparently can be considerate as a model for pharmacokinetic evaluation of varenicline.

scholarly journals Analgesic and Neuropharmacological Investigations of the Aerial Part of Achyranthes aspera Linn.

1970 ◽  
Vol 1 (1) ◽  
pp. 44-50 ◽  
Author(s):  
Md Ashraful Alam ◽  
Nazmuj Slahin ◽  
Riaz Uddin ◽  
SM Raquibul Hasan ◽  
Raushanara Akter ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Acetic Acid ◽  
Open Field ◽  
Field Test ◽  
Open Field Test ◽  
Sleeping Time ◽  
Achyranthes Aspera ◽  
Central Nervous System Depressant ◽  
Thiopental Sodium

Analgesic and central nervous system depressant activity of the methanol extract of Achyranthes aspera Linn. was assessed by using acetic acid induced writhing test, thiopental sodium induced sleeping time determination, hole cross test and open field test in albino mice. The extract (250 and 500mg/kg) showed a dose dependent inhibition of writhing response generation by acetic acid compared to reference drug diclofenac sodium (50mg/kg). Methanol (70%) extract of Achyranthes aspera (500 mg/kg) also produced rapid onset and maximized the duration of sleeping time when administered with thiopental sodium. The extract also decreased the motor activity and exploratory behavior of mice in hole cross and open field test. The overall experimental results suggest the analgesic and central nervous system depressant activity of the methanolic extract of Achyranthes aspera and justify its use in folkloric remedies. Key Words: Achyranthes aspera, Analgesic activity, Central nervous system depressant activity. doi:10.3329/sjps.v1i1.1807 S. J. Pharm. Sci. 1(1&2): 44-50

scholarly journals Pharmacological activity of new imidazole-4,5-dicarboxylic acid derivatives in dopaminergic transmission suppression ttests in mice and rats

2020 ◽  
Vol 6 (4) ◽  
pp. 51-57
Author(s):  
Ekaterina E. Yakovleva ◽  
Eugeny R. Bychkov ◽  
Maria M. Brusina ◽  
Levon B. Piotrovsky ◽  
Petr D. Shabanov
Keyword(s):  
Locomotor Activity ◽  
Dicarboxylic Acid ◽  
Open Field ◽  
Field Test ◽  
Open Field Test ◽  
Dicarboxylic Acids ◽  
Dopaminergic Transmission ◽  
Dose Dependent ◽  
Derivatives Of ◽  
Experimental Improvement

Objective: To study the antiparkinsonian activity of new 1,2-substituted imidazole-4,5-dicarboxylic acids in dopaminergic transmission suppression tests in mice and rats. Materials and methods: On a model of reserpine extrapyramidal disorders, the derivatives of imidazole-dicarboxylic acids (IEM2258, IEM2248, IEM2247) were injected into the lateral brain ventricles of the mice 30 minutes after injecting reserpine at the doses of 0.1–0.5 mmol. Locomotor activity was analyzed in the Open-field test 2 hours later. In the catalepsy model, the studied agents were injected, using a pre-implanted cannula, with a simultaneous intraperitoneal injection of haloperidol. The severity of catalepsy was assessed with the Morpurgo method. Amantadine was used as a comparator drug in all the tests. Results: It was shown that IEM2258 significantly increased the main indicators of locomotor activity in the Open-field test at all the studied doses. The value of the antiparkinsonian effect of IEM2258 at doses of 0.4–0.5 mmol significantly exceeded that of amantadine. The antiparkinsonian effect of IEM2247 was maximally expressed and was significantly different from those in the control and comparator group at doses of 0.2 and 0.3 mmol. For all the experimental groups, a significant decrease in the manifestations of catalepsy in comparison with control indexes was determined. Discussion: The results made it possible to suggest the involvement of imidazole-4,5-dicarboxylic acids derivatives in the process of experimental improvement of dopaminergic neuromodulation and efficiency in animals. Conclusion: The data showed a significant dose-dependent antiparkinsonian activity of new imidazole-4,5-dicarboxylic acid derivatives, which makes it promising to develop these agents and to further search for effective and safe antiparkinsonian drugs in this pharmacological class. Graphical abstract

scholarly journals Monoaminergic Involvement in Decreased Locomotor Activity of Mice Treated with α and β-amyrin from Protium heptaphyllum

2018 ◽  
Vol 13 (8) ◽  
pp. 1934578X1801300
Author(s):  
Gislei F. Aragão ◽  
Manoel O. de Moraes Filho ◽  
Paulo N. Bandeira ◽  
Antônio P. Frota Junior ◽  
Yasmin Ingrid S. Oliveira de ◽  
...  
Keyword(s):  
Cerebral Cortex ◽  
Locomotor Activity ◽  
Open Field ◽  
Field Test ◽  
High Performance ◽  
Open Field Test ◽  
Inhibitory Effect ◽  
Pharmacological Agents ◽  
Tissue Homogenates ◽  
The Central Nervous System

A triterpenic mixture of α and β-amyrin (AMY) extracted from Protium heptaphyllum has demonstrated several pharmacological effects, including activity in the central nervous system. The aim of this study was to evaluate the effect of AMY administration on locomotor activity of mice by the open field test using some monoaminergic agonists and antagonists and the cerebral cortex levels of monoamines and their major metabolites by high-performance liquid chromatography. Mice were treated acutely with AMY at doses of 1, 2.5 and 5 mg/kg given intraperitoneally and with the pharmacological agents and placed in open field test, then the animals were sacrificed and the cerebral cortex extracted, and monoamines were assayed in tissue homogenates. AMY at 1, 2.5 and 5 mg/kg decreased locomotor activity of animals by 25, 31 and 39%, respectively in the open field test. Ondasentron, doxazosin, oxymetazoline and clonidine did not reverse the inhibitory effect of 5 mg/kg AMY. Venlafaxine and yohimbine reversed the inhibitory effect of 5 mg AMY. In the cortex, the 5-HT and 5-HIAA were significantly reduced by the administration of AMY. NE and HVA were also reduced with 2.5 and 5 mg/kg AMY, while Dopamine and DOPAC were not increased with AMY. In conclusion, AMY decreased locomotor activity of animals accompanied by a decrease in 5-HT and NE levels in the cerebral cortex, this locomotor effect is reversed by drug that blocker the α-2-adrenoreceptor.

scholarly journals Broiler Response to Open Field Test in Early Ontogeny

2010 ◽  
Vol 79 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Linda Balážová ◽  
Eva Baranyiová
Keyword(s):  
Locomotor Activity ◽  
Open Field ◽  
Field Test ◽  
Repeated Measures ◽  
Broiler Chickens ◽  
Open Field Test ◽  
Early Ontogeny ◽  
Visual Orientation ◽  
Novel Environment ◽  
Post Hoc

The aim of this study was to observe the development of exploratory behaviour in growing broilers, i.e. their reaction to a novel environment (habituation) during the post-incubation period. Twelve males and twelve females of ROSS 308 line were kept from hatching until 42 days of age in separate pens, under identical husbandry conditions. To study their behaviour, we used the open-field test (OFT). Individual 10-min tests were initiated at the age of 3 days, and were repeated at weekly intervals, i.e. a total of 6 tests were carried out. The results were evaluated using analysis of variance (ANOVA) for repeated measures and Tukey post-hoc test. Broilers of both sexes were most active during the first OFT on day 3 after hatching. In male broilers, we found a significant decrease in all exploratory activities between the first and 2nd OFT; duration of their horizontal locomotor activity was reduced from 104 ± 51.86 s to 3.50 ± 3.50 s (p < 0.05), duration of visual orientation decreased from 327.50 ± 55.94 s to 125.00 ± 31.94 s (p < 0.001), and duration of vocalizations decreased from 412.50 ± 63.12 s to 90.00 ± 34.25 s (p < 0.001). In females, a significant decrease was observed betwen the first and 2nd OFT only in duration of horizontal locomotor activity that decreased from 234.25 ± 52.07 s to 14.25 ± 8.36 s (p < 0.001) and between the first and 3rd OFT in duration of vocalization (decreasing from 430.00 ± 66.30 s in 1st OFT to 60.00 ± 23.35 s; p < 0.001). On the other hand, a significant increase in duration of comfort behaviour was noted between the first and second OFT in both sexes (in males from 95.00 ± 40.76 s to 462.50 ± 38.81 s; p < 0.001; in females from 85.00 ± 31.73 s to 437.50 ± 67.74 s; p < 0.001). Changes in defecation numbers were not significant in either sex. Our findings show that the most profound changes in behaviour of broiler chickens occurred between the first and second OFT, that male broilers used visual orientation in the open field arena more than females in the first test, they vocalized less in the second test, and they seem to have habituated to the novel environment earlier than females.

scholarly journals Analgesic Effects and Impairment in Locomotor Activity Induced by Cannabinoid/Opioid Combinations in Rat Models of Chronic Pain

2020 ◽  
Vol 10 (8) ◽  
pp. 523
Author(s):  
Mohammad Alsalem ◽  
Ahmad Altarifi ◽  
Mansour Haddad ◽  
Belal Azab ◽  
Heba Kalbouneh ◽  
...  
Keyword(s):  
Chronic Pain ◽  
Neuropathic Pain ◽  
Locomotor Activity ◽  
Open Field ◽  
Field Test ◽  
Inflammatory Pain ◽  
Open Field Test ◽  
Antinociceptive Effect ◽  
Synthetic Cannabinoids ◽  
Antinociceptive Effects

Both opioids and cannabinoids have well-known antinociceptive effects in different animal models of chronic pain. However, unwanted side effects limit their use. The aim of this study is to evaluate the antinociceptive effect of combining synthetic cannabinoids with subtherapeutic doses of opioids, and to evaluate the effects of these drugs/combinations on rat’s locomotor activity. Intra-plantar injection of Complete Freund’s Adjuvant (CFA) into the left hindpaw and intraperitoneal injection of streptozotocin (STZ) were used to induce inflammatory and diabetic neuropathic pain in adult male Sprague-Dawley rats, respectively. Von Frey filaments were used to assess the antinociceptive effects of opioids (morphine and tramadol) and the synthetic cannabinoids (HU210 and WIN55212) or their combinations on CFA and STZ-induced mechanical allodynia. Open field test was used to evaluate the effect of these drugs or their combinations on locomotion. HU210 and WIN55212 did not produce significant antinociceptive effect on inflammatory pain while only the maximal dose of HU210 (1 mg/kg) was effective in neuropathic pain. Only the maximal doses of morphine (3.2 mg/kg) and tramadol (10 mg/kg) had significant anti-allodynic effects in both models. Tramadol (1 mg/kg) enhanced the antinociceptive effects of WIN55212 but not HU210 in neuropathic pain with no effect on inflammatory pain. However, in open field test, the aforementioned combination did not change tramadol-induced depression of locomotion. Tramadol and WIN55212 combination produces antinociceptive effects in neuropathic but not inflammatory pain at low doses with no additional risk of locomotor impairment, which may be useful in clinical practice.

scholarly journals Genotype-Dependent Difference in 5-HT2CReceptor-Induced Hypolocomotion: Comparison with 5-HT2AReceptor Functional Activity

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Darya V. Bazovkina ◽  
Elena M. Kondaurova ◽  
Vladimir S. Naumenko ◽  
Evgeni Ponimaskin
Keyword(s):  
Locomotor Activity ◽  
Open Field ◽  
Field Test ◽  
Serotonin Receptor ◽  
Open Field Test ◽  
Inbred Mouse ◽  
Receptor Activation ◽  
Mouse Strains ◽  
Functional Responses ◽  
Mk 212

In the present study behavioral effects of the 5-HT2Cserotonin receptor were investigated in different mouse strains. The 5-HT2Creceptor agonist MK-212 applied intraperitoneally induced significant dose-dependent reduction of distance traveled in the open field test in CBA/Lac mice. This effect was receptor-specific because it was inhibited by the 5-HT2Creceptor antagonist RS102221. To study the role of genotype in 5-HT2Creceptor-induced hypolocomotion, locomotor activity of seven inbred mouse strains was measured after MK-212 acute treatment. We found that the 5-HT2Creceptor stimulation by MK-212 decreased distance traveled in the open field test in CBA/Lac, C57Bl/6, C3H/He, and ICR mice, whereas it failed to affect locomotor activity in DBA/2J, Asn, and Balb/c mice. We also compared the interstrain differences in functional response to 5-HT2Cand 5-HT2Areceptors activation measured by the quantification of receptor-mediated head-twitches. These experiments revealed significant positive correlation between 5-HT2C and 5-HT2A receptors functional responses for all investigated mouse strains. Moreover, we found that 5-HT2Areceptor activation with DOI did not change locomotor activity in CBA/Lac mice. Taken together, our data indicate the implication of 5-HT2Creceptors in regulation of locomotor activity and suggest the shared mechanism for functional responses mediated by 5-HT2Cand 5-HT2Areceptors.

scholarly journals Like Mother Like Child: Do Fearful Sows Have Fearful Piglets?

Animals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1232
Author(s):  
Hazel B. Rooney ◽  
Oceane Schmitt ◽  
Alexandra Courty ◽  
Peadar G. Lawlor ◽  
Keelin O’Driscoll
Keyword(s):  
Open Field ◽  
Field Test ◽  
Open Field Test ◽  
Age And Growth ◽  
Maternal Behaviour ◽  
Human Contact ◽  
Fear Level ◽  
Behavioural Profile ◽  
D 20 ◽  
Gestational Stress

Gestational and early life experiences affect subsequent behavioural and physical development. The objective of the current study was to investigate associations between gilts’ fear of humans, gestational stress level, and feeding and maternal behaviour, as well as how these related to aspects of the personality and growth of their offspring. A total of 37 gilts were used. Four human approach tests were performed between d 104 and d 111 of gestation to classify gilts as fearful or friendly. Gilt feeding behaviour and salivary cortisol concentration was measured between d 90 and d 108 of gestation, and gilt nursing behaviour assessed at d 13 of lactation. Piglets were subject to a back test at d 13 of age, to an open field test and a human approach test at d 20 of age, and growth was monitored to weaning (d 26 of age). Gilts classified as having a fearful behavioural profile had higher cortisol levels than friendly gilts (p < 0.05). Human fear level did not affect reproductive performance or the growth of offspring (p > 0.05). The offspring of friendly gilts tended to have a more active response to the back test (p = 0.09), less freezing response in the open field test (p < 0.05), and received human contact more than piglets from fearful gilts (p < 0.05). The present study shows that gilt human fear level is linked to their stress levels, which can affect the personality of their piglets.

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