Evaluating the effect of pentazocine and dextromethorphan on progesterone induced depression in female mice

Background and aims: Progesterone is a female reproductive hormone. Increasing progesterone levels during menstruation or taking synthetic progesterone in oral contraceptives causes some depression in some women. Sigma receptors are considered as new targets in depression medication. Progesterone other than hormonal effects is a neuro-steroid and is an antagonist to sigma receptors. So, the aim of the current study was to investigate the effect of co-concomitant use of progesterone with sigma agonist drugs, dextromethorphan or pentazocine on depression test. Methods: This research is a basic- applied study. Experiments were performed on female mice weighing 25-30 g. The forced swimming test was used to investigate depression. Progesterone 10 mg/kg along with dextromethorphan HBr 30 mg/kg, or pentazocine 2.5 mg/kg were administered on the first day and 30 min before the FST on the second day. Data were analyzed using One-way ANOVA and Tukey tests. Results: Progesterone led to an increase in the immobility time (over 3 minutes) in mice, which is a criterion for animal depression (P<0.05). The immobility of animals was decreased by following consumption of dextromethorphan (100s±13) (P<0.001), and pentazocine (124s±6.9) (P<0.01). These changes were in parallel with antidepression medications by fluvoxamine. Conclusion: Since depression caused by progesterone is resolved by Sigma agonists, Sigma receptors are responsible for depression caused by high doses of progesterone. So, these agonists can be considered as an effective antidepressant in progesterone medications with high dose

Age related interaction of dopamine and serotonin synthesis in striatal synaptosomes

Tyrosine hydroxylase and tryptophan hydroxylase are key rate limiting enzymes in the biosynthesis of dopamine and serotonin, respectively. Since both enzymes are active in striatum, and affected by age, this study was undertaken to investigate interaction between dopamine and serotonin synthesis in brain striatal synaptosomes of aging rat. Male Wistar rats (3 and 30 month old) were killed by decapitation and brain striatal synaptosomes were prepared by discontinuous Ficoll/sucrose gradient technique. Synaptosomes were incubated in the presence of added pargiline (monoamineoxidase inhibitor), dopamine or serotonin synthesized during 25 min was measured by HPLC, employing electrochemical detection. Dopamine synthesis in synaptosomes prepared from young animals was markedly inhibited by addition of 5 μM serotonin concentrations (30) and increasing serotonin concentrations up to 50 μM caused only a smaller additional inhibition. Dopamine synthesis in synaptosomes obtained from old rats was significantly lower than that of youg animals and addition of serotonin concentrations up to 50 μM had little effect on these preparations. In case of serotonin synthesis, exogenously added 5 μM dopamine inhibited serotonin synthesis in the synaptosomes of both ages by about 40, whereas with higher concentration of dopamine (10-50 μM) the rate of inhibition was highly pronounced in old rats as compared to that of young animals. It is concluded that dopamine and serotonin interaction may be significant, and that these should be considered in long-term treatments of Parkinson's disease with L-DOPA

COMPARING THE EFFECT OF CLOFIBRATE AND PHENOBARBITAL ON THE NEWBORNS WITH HYPERBILIRUBINEMIA

The aim of treating hyperbilirubinemia is preventing the serum bilirubin to reach neurotoxic levels, which is done by phototherapy or blood transfusion. However, pharmacological treatments still remain vague. Therefore the effects of adding either clofibrate or phenobarbital on treatment outcomes was evaluated in icteric non-hemolitic newborns. Ninety neonates were divided in three groups. Two groups were prescribed 100 mg/kg clofibrate or 5 mg/kg phenobarbital orally as single dose on arrival, in addition to phototherapy. The control group only received phototherapy. Serum bilirubin was evaluated at the reception and 12, 24, 48 and 72 hours after beginning of drug therapy. Total bilirubin levels decreased in treated groups compared with the control group in all samples taken (12, 24, 48 and 72 hours). Clofibrate effect in decreasing bilirubin level was more prominent (14 % and 32 % after 12 and 72 h respectively). In addition duration of hospitalization and length of phototherapy decreased in clofibrate and phenobarbital groups compared with control group (1.5, 2 days respectively, vs. 2.6 days). Therefore using clofibrate and phenobarbital in icteric neonates are supportive not only by decreasing the serum bilirubin level, but also by lessening the duration of hospitalization and phototherapy. Thus in addition to cost benefits for the patient these drugs can reduce the risks of transfusion, and clofibrate seems more promising in this regard

The effects of increasing PGE2 on translocation of labeled albumin into rat brain

Under pathophysiological conditions, infiltration of leukocyte plays a key role in the progressionof the neuroinflammatory reaction in the CNS. Prostaglandin E2 (PGE2) is known to accumulate at lesion sites of the post-ischemic brain. Although post-ischemic treatments with cyclooxygenase-2 inhibitors reduce blood-brain barrier (BBB) leukocyte infiltration, the direct effect of PGE2 on BBB has not been fully implemented. Therefore, the direct effect of increasing PGE2 infusion on translocation of labeled albumin into the brain was assessed. Under anesthesia rats were drilled stereo-taxicaly a burr hole in the right forebrain and PGE2 was infused into the forebrain and the hole was occluded. The animals were then injected with fluorescent labeled albumin (FA), via internal right jugular vein and decapitated at different infusion time points. The forebrain was removed and each forebrain hemisphere was homogenized and fluorescence intensities were measured in the supernatant. The fluorescence intensities measured in the right and left forebrain hemispheres of the control group (0.0 µg PGE2) were almost identical. Four hours after infusion of PGE2 at doses higher than 250 µg, fluorescence intensity increased in the right forebrain supernatant, even if it was not statistically significant. The fluorescence intensity was detectable in the brain supernatant 4 h after infusion of PGE2 in doses higher than 250 µg PGE2. The highest fluorescence intensity was 16 h after infusion of 500 µg PGE2, which returned to near control values after 48 h. Increased fluorescence intensity in the brain following PGE2 infusion is concluded to be associated with disruption of the BBB

The effects of Anethum graveolens essence on scopolamine-induced memory impairment in mice

Since Anethum graveolens (Dill) has phytoestrogenic compounds and it is proven that estrogens exert beneficial effects on cognition; the aim of this study was to understand if this plant can improve memory performance. Male Balb/c mice weighing 25-30 g were used in this study and memory was assessed by the novel object recognition task. In this method, the difference in the exploration time between a familiar object and a novel object is taken as an index of memory performance (recognition index, RI). Scopolamine significantly reduced memory index (RI = -15.5% ± 3.0). Dill essence (100 mg/kg, ip) prevented the harmful effects of scopolamine on memory (RI = 40% ± 5.5), thus RI did not differ with control animals (RI = 50% ± 5.8). In addition, 17-β estradiol also prevented memory impairment in animals (0.2 mg/kg, ip; RI = 35.8% ± 6.5). Nevertheless, the beneficial effects of dill essence were antagonized by prior injection of tamoxifen (1 mg/kg, ip; RI = -30% ± 7.8). Although phytoesrogens are not steroids, the beneficial effect of dill on memory, at least in part, may have been achieved by estrogenic receptors present in the brain. Thus dill essence could be promising in improving memory and cognition, mainly in postmenopausal women

The effect of Cinnamomum zeylanicum bark water extract on memory performance in alloxan-induced diabetic mice

Cinnamomum zeylanicum (cinnamon) has a wide range of beneficial effects including mild glucose lowering activity. The aim of the present study was to investigate whether cinnamon bark extract has the potential to improve memory performance and glucose profiles in diabetic mice. Memory was assessed by the novel object recognition task in male Balb/c mice. In this method, the difference between exploration time of a familiar object and a novel object was considered as an index of memory performance (recognition index, RI). The water extract was prepared by boiling cinnamon bark for 15 min. Alloxan induced diabetes in animals (serum glucose levels were 322 ± 7.5 mg/dL), and also impaired memory performance (RI= -3.3% ± 3.3) which differed significantly from control animals (RI = 32% ± 6.5). Although treatment with cinnamon only reduced fasting blood glucose level moderately but it improved memory performance remarkably (RI = 25.5% ± 5.6). Oxidative stress following administration of cinnamon extract was lower in diabetic mice. It was concluded that cinnamon water extract could be a useful alternative medicine in diabetic patients' daily regimen which not only reduces blood glucose levels but also improves memory performance and lipid peroxidation level

Evaluating the effect of foeniculum vulgar on scopolamin-induced memory impairment in Male Mice

Background: Estrogen is a steroid that regardless of its obvious effects on females’ reproductive functions shows beneficial effects on cognition. Foeniculum vulgar (fennel) has phytoestrogen compounds that might be beneficial in memory performance. This research was performed to understand if this plant can improve memory. Methods: To evaluate memory, novel object recognition task was used in male Balb-c mice, which comprised of three sections: habituation, learning trial (T1) and the test trial (T2). In this method, the difference in the exploration time between a familial (F) and a novel (N) object is taken as an index of memory performance [recognition index (RI) = (N – F)/(N + F) × 100]. Findings: Memory was harmed using 0.5 mg/kg subcutaneous scopolamine [RI (%) = -16.0 ± 3.0]. 50 mg/kg intraperitoneal fennel considerably prevented memory impairment of scopolamine [RI (%) = 35.0 ± 7.1] and this was parallel with the memory index in normal animals [RI (%) = 50.0 ± 5.8]. In addition, 0.2 mg/kg intraperitoneal 17-β estradiol showed similar results as fennel on memory protection [RI (%) = 36.0 ± 6.6]. However, the beneficial effects of fennel were impaired by prior intraperitoneal injection of 1 mg/kg tamoxifen [RI (%) = -29.0 ± 7.1]. Conclusion: The beneficial effect of fennel on memory is achieved by estrogenic receptors present in the brain; by stimulating these receptors, they could cause an increase in acetylcholine release. Therefore, it can competitively prevent the antagonizing effect of scopolamine on cholinergic receptors. © 2015, Isfahan University of Medical Sciences(IUMS). All rights reserved. Evaluating the effect of foeniculum vulgar on scopolamin-induced memory impairment in Male Mice. Available from: https://www.researchgate.net/publication/282273930_Evaluating_the_effect_of_foeniculum_vulgar_on_scopolamin-induced_memory_impairment_in_Male_Mice [accessed Jul 29, 2017]

Nerve growth factor receptors in dementia

Background/aim: Nerve growth factor (NGF) promotes the survival and differentiation of sensory and sympathetic neurons. Several studies have found that certain neuropathological factors stimulate NGF receptor expression and release the truncated nerve growth factor receptor (TNGFR) to biological fluids. The aim of this pilot study was to determine urine TNGFR levels in patients with dementia and to verify whether TNGFR can be used as a biomarker of dementia. Materials and methods: Twelve patients with dementia and 12 healthy individuals were asked to voluntarily participate in this study. Ages, sexes, and weights were matched. The first morning urine samples were collected and the concentrations of TNGFR in the urine samples were measured by fluoroimmunoassay. Results: The mean levels of TNGFR in the urine samples of the healthy control subjects and the patients with dementia were 164 +/- 23 and 341 +/- 66 ng / mg creatinine respectively. A positive relationship was found between the levels of TNGFR in different ages of both control and patient subgroups. This is consistent with the previous observations that pathological condition may stimulate the NGF receptor expression. Conclusion: These findings might be of assistance to evaluate the development of the memory loss associated with Alzheimer disease and other age-associated diseases

A Review on Ethnobotanical and Therapeutic Uses of Fenugreek (Trigonella foenum-graceum L)

Fenugreek with the scientific name of Trigonella foenum-graceum L and with leaves consisting of 3 small obovate to oblong leaflets is an annual herbaceous plant of the Fabaceae family. It is native to the eastern Mediterranean but is cultivated worldwide. This plant has medicinal alkaloids, steroid compounds, and sapogenins and many uses have been mentioned for this plant in traditional medicine. This plant has been used to ease childbirth, to aid digestion, and as a general tonic to improve metabolism. Trigonelline is considered as the most important metabolite of fenugreek, which is very effective in treating diabetes and decreasing blood cholesterol. Diaszhenin is another important compound in seeds of this plant, which is used in producing medicinal steroids like contraceptive pills. Many studies have been performed on the therapeutic effects and identification of chemical compounds of this plant. In this article, the most important biological effects and reported compounds about fenugreek seed are reviewed and its therapeutic applications are investigated. © 2015, © The Author(s) 2015

Evaluation of the effect of soybean diet on interferon-α-induced depression in male mice

Objective: Interferon-α (IFN) therapy can cause depressive symptom which may lead to drug discontinuation. By interfering with tryptophan pathway, the available level of tryptophan required for serotonin synthesis decreases which could be related to depression. The aim of this study was to evaluate whether soybean diet could improve IFN-induced depression. Materials and Methods: Male mice weighing 28±3 g were used in the forced swimming test (FST) as an animal model of depression; also, locomotor activity was recorded. IFN 16×105 IU/kg was injected subcutaneously for 6 days. Animals were fed with regular diet or soybean diet at 3 concentrations throughout the experiment. Fluoxetine was the reference drug. To check whether the tryptophan content in the soy bean diet was effective, a group of animals was injected with a single dose of tryptophan on the test day. Results: IFN-α increased the immobility time in the FST (192 sec ± 5.4), that denotes depression in mice. Soybean diets caused less immobility that was more profound with 50% soybean (26.4 sec ± 6). This diet overcame the depression caused by IFN in the FST (54 sec±18). This result was parallel with that of tryptophan injected to animals (38 sec±17). All the animals showed normal locomotor activity. Conclusion: For the first time, we showed that soybean diet could counteract with depression caused by IFN-α. Since tryptophan therapy had similar effects, possibly the tryptophan content of soybean had induced the serotonin synthesis. Thus, not only less harmful kynurenine was produced but also more serotonin was available in the brain to overcome depression. However, this interpretation needs further evaluations