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CBD FAQ – Cannabidiol Frequently Asked Questions

Analysis of Anxiety and Rodent CBD in Stress



  • Analysis of Anxiety and Rodent CBD in Stress
  • CBD For Anxiety
  • Introduction
  • CBD has been studied in a wide range of animal models of general anxiety, including All further studies of acute systemic CBD without prior stress showed anxiolytic .. Dynamic causal modeling analysis in this data set further showed CBD. Paradigms for testing of anxiety-like behaviors in rodents In fact, the THC: CBD ratio is the main criterion to define different cannabis chemotypes .. age, gender , environmental stress and concurrent use of other drugs; a detailed analysis of. Repeated-measures analyses of variance showed that the TPSRS However, several animal studies have shown that CBD produces inverted . 80, Pre-stress (P), Measurements, VAMS-anxiety and sedation, blood.

    Analysis of Anxiety and Rodent CBD in Stress

    In some experiments AM 1. Mouse brains were perfused after behavioural analyses and processed for immunofluorescence analysis. Different mild stressors were used randomly: The NSF behaviour test was performed in a 5 min test session as previously described Santarelli et al.

    Twenty-four hours before the test, all animals were food deprived. On the day of the test a single regular chow pellet was placed in a white platform located in the middle of the box.

    Each animal was placed in one of the apparatus corners and the latency to start to eat in the new environment was measured. The stopwatch was immediately stopped when the mouse bit the chow, using its forepaws sitting on its haunches. After the test all animals were returned to their home cages and the amount of food consumed in 5 min was measured. Basal feeding latency of control mice differed in separate CUS experiments Figs.

    As these experiments were performed in different laboratories Brazil and Spain , it is conceivable that differences in animal housing, environment and handling conditions are responsible for this. Entries in the enclosed arms were also quantified c.

    At the beginning of the test, each mouse was placed in the central area of the apparatus with its head facing an enclosed arm. The Anymaze software Stoelting Co. It detects the position of the animal in the maze and calculates the number of entries and time spent in open and enclosed arms.

    Enclosed-arm entries were considered as an indicator of locomotor activity, whereas percentage of time spent in open arms and percentage open-arm entries were used as measures of anxiety. Tris HCl 50 m m pH 7. The organic and aqueous layers were separated by centrifugation g , 2 min and the organic layer transferred to a clean vial and dried under a stream of argon. The gradient elution mobile phases consisted of A The gradient flow rate of 0.

    MS analysis was performed with an electrospray ionization source. The capillary voltage was set to 3. LC-MS measurements were made by selected ion monitoring in positive mode.

    Briefly, after 1 h blockade with PBS supplemented with 0. Doublecortin immunoreactivity was detected by the avidin—biotin immunoperoxidase method Vectastain ABC kit; Vector Lab, USA and the product of the reaction was revealed by adding the chromogen 3,3-diaminobenzidine tetrahydrochloride Sigma Chemical, USA.

    In vivo , BrdU- and doublecortin-positive cells were quantified in the subgranular zone of the hippocampus in a minimum of five coronal sections per animal. A 1-in series of hippocampal sections located between 1. The absolute number of positive cells was calculated considering the total hippocampal volume as determined by the sum of the areas of the sampled sections multiplied by the distances between them.

    Doublecortin immunoreactivity was quantified using a computerized image analysis system ImagePro software. The HiB5 hippocampal progenitor cell line was grown as described Palazuelos et al. Cells were grown in polyornithine-coated plates.

    Stock solutions were prepared in dimethylsulfoxide. No significant influence of vehicle on any of the variables measured was observed at the final concentration used 0.

    Control incubations included the corresponding vehicle content. Ten thousand cells per analysis were recorded. Significant differences between the groups were evaluated by t test, one, two or three-way analysis of variance ANOVA test, followed by Duncan's post hoc test.

    To investigate the mechanism by which CBD exerts its anxiolytic effects and, in particular, its relation to hippocampal neurogenesis, we first exposed WT mice to a CUS model and CBD or vehicle was administered i.

    CUS inhibited adult hippocampal neurogenesis as determined by quantification of BrdU-positive and doublecortin-expressing cells Fig. This approach allowed us to investigate the consequence of blocking adult hippocampal progenitor cell proliferation by GCV administration Garcia et al. Chronic unpredictable stress CUS -induced reduction of hippocampal neurogenesis is attenuated by cannabidiol CBD administration. Two-way analysis of variance followed by Duncan's post hoc test. Cannabidiol CBD administration exerts a proneurogenic effect.

    Representative immunofluorescence images are shown. Analysis of the EPM test in stressed animals showed that in WT mice CBD promoted an anxiolytic-like effect by increasing the percentage of entries and time spent in the open arms Fig.

    No effect in the number of enclosed-arm entries was found Fig. These results evidenced that repeated CBD administration exerts an anxiolytic-like effect in mice subjected to CUS and that this occurs in parallel with changes in hippocampal neurogenesis. Considering the diversity of molecular targets that have been proposed to mediate CBD actions Izzo et al. No effect of CBD in the number of enclosed-arm entries was found Fig. We therefore evaluated if CBD modulates the eCB tone, as previously suggested, by inhibiting anandamide degradation Bisogno et al.

    To investigate the mechanism of action of CBD on neural progenitor cells, we used the HiB5 hippocampal progenitor cell line, which provides a good model to investigate the mechanism of action of cannabinoids as they express CB 1 and CB 2 cannabinoid receptors when cultured in proliferating conditions Palazuelos et al.

    Based on previous reports Campos and Guimaraes, ; Zanelati et al. The CB 2 antagonist alone exerted a paradoxical slight increase in cell proliferation. These results indicate that HiB5 cells express functional eCB receptors that can be activated indirectly by CBD and drive progenitor cell proliferation.

    Results are provided as percentage of total cells. Representative images are shown. Results correspond to three independent experiments. Overall, these results show that eCBs promote hippocampal progenitor proliferation and this effect can be mimicked by CBD, whose action relies on CB receptor engagement. The results shown herein contribute to the elucidation of the cellular and molecular mechanisms involved in the anxiolytic effect of chronic CBD administration.

    Specifically, genetic ablation of proliferating progenitors in the adult mouse brain prevents CBD anxiolytic action, thus demonstrating the requirement of hippocampal neurogenesis. Taken together, our findings strongly support that chronic CBD administration exerts an anxiolytic and proneurogenic hippocampal action by increasing the eCB tone.

    CBD is a plant-derived cannabinoid of high interest owing to its anxiolytic, antipsychotic and antidepressive actions evidenced in human studies as well as in animal models Izzo et al. For example, CBD is effective for the management of some symptoms of schizophrenia and psychosis with less adverse effects than other antipsychotics Leweke et al.

    The beneficial effects of CBD administration in psychiatric symptoms adds to its safe profile in humans and the existence of CBD-containing standardized medicines e. Sativex and well-defined administration routes e. However, the mechanism of CBD action is complex and remains obscure, as many targets have been shown to be candidates for its behavioural actions. CBD can facilitate eCB-mediated neuromodulation by decreasing anandamide hydrolysis or re-uptake Bisogno et al.

    Other acute anxiolytic and antidepressant effects of CBD seem to depend on facilitation of 5-HT 1A receptor-mediated neurotransmission Campos and Guimaraes, ; Gomes et al.

    The present study supports that the proliferative effects of CBD on hippocampal progenitors are mediated by CB 1 and CB 2 receptors secondary to an increased eCB tone resulting from the inhibition of anandamide deactivation. N -acylethanolamine-hydrolyzing acid amidase and their different bulk levels. Our findings are in agreement with a recent study reporting that CBD-induced hippocampal neurogenesis is absent in CB 1 -receptor knockout animals Wolf et al.

    Thus, like CBD, anandamide- and 2-arachidonoylglycerol-degradation inhibitors promote hippocampal progenitor proliferation and neurogenesis Aguado et al.

    CBD, as well as other cannabinoids, produce typically bell-shaped dose—response curves, as seen here in vitro in proliferative experiments. Higher CBD concentrations can activate TRPV1 receptors and this effect has been associated by the lack of anxiolytic action observed with these doses Campos and Guimaraes, The importance of the eCB system, and, in particular, of CB 1 receptors, in mood control and depressive behaviours has been investigated for decades Hill et al.

    Plant-derived cannabinoids exert a wide variety of effects on depressive and anxiety behaviours Izzo et al. Alterations of the eCB system such as changes in CB 1 receptor expression and eCB levels are associated with major depression and suicide commitment Hungund et al. An emerging paradigm from cannabinoid research is that the eCB system constitutes an allostatic signalling system that contributes to cellular plasticity responses in adaptation to stress-induced alterations Patel and Hillard, Indeed, stress induces an inhibitory effect on neurogenesis that can be partially reverted by engaging the eCB system Hill et al.

    The role of adult neurogenesis in the regulation of cognition and mood is the object of intense study since the initial discovery of the adult hippocampal neurogenic niche David et al. Blockade of hippocampal neurogenesis prevents some of the beneficial effects of antidepressant drugs and stimuli, although its ablation is not sufficient to induce depression and anxiety. However, blockade of adult neurogenesis makes mice more susceptible to stress-induced depressive behaviours Snyder et al.

    Pharmacological manipulation and inducible genetic expansion of adult neurogenesis can improve depressive or anxiety-related behavioural changes Santarelli et al. Thus, the emerging scenario indicates that adult hippocampal neurogenesis is involved in the plastic processes that allow for adaption to environmental changes Dranovsky et al. Accordingly, by using transgenic GFAP-TK or hippocampus-irradiated mice, it has been demonstrated that inhibition of adult neurogenesis increases hypothalamic-pituitary-adrenal axis activity and glucocorticoid resistance Snyder et al.

    The stress-induced anxiogenic response as determined in the NSF test is buffered by adult-born hippocampal neurons and, reciprocally, the neurogenic niche influences hippocampal progenitor cell fate Dranovsky et al.

    Our results indicate that chronic CBD administration, by promoting neurogenesis, favours a similar anxiolytic response in stressed mice. This result agrees with previous reports showing that adult neurogenesis does not alter NSF behaviour under baseline conditions Snyder et al. In our study, however, the animals were tested 24 h after drug injection. This suggests that repeated CBD administration prevents the effects of CUS rather than induces an acute anxiolytic effect.

    Antidepressive stimuli such as environmental enrichment and voluntary wheel running exert a proneurogenic action that has been shown to depend on the presence of functional CB 1 receptor signalling Hill et al. Voluntary running increased CB 1 receptor binding sites as well as anandamide levels in the hippocampus, but not in the prefrontal cortex, and administration of the CB 1 antagonist AM prevented running-induced proliferation Hill et al. The role of CB 1 receptors in hippocampal neurogenesis, however, could be more complex, since spatially and locally restricted eCB signalling induction by CBD is proneurogenic, THC failed to promote or even inhibited adult neurogenesis Wolf et al.

    This latter effect may be related to the spatial learning impairments caused by THC, an effect that is absent in animals treated with CBD Fadda et al.

    In agreement with the hypothesis that the anxiolytic effect of repeated administration of CBD in the CUS model is mediated by the proneurogenic action of the CB 1 receptor, pharmacological blockade of this receptor blunted the behavioural effect of CBD.

    CB 2 cannabinoid receptor agonists are also suitable candidates to promote neural progenitor proliferation Palazuelos et al. Ageing-associated decline of hippocampal and olfactory bulb neurogenesis can be prevented by the CB 2 receptor-selective agonist JWH Goncalves et al.

    Overall, CBD is safe to use at low to high doses since standardized dosage limits have yet to be established.

    Some adjustment may be necessary to realize the right dose for the personal situation. CBD is ideal for people that prefer not to feel high. Cannabinoids are responsible for mood regulation, pain sensation, as well as regulation of appetite and proper functioning of the memory.

    CBD can raise the levels of naturally-produced cannabinoids in the body called the endocannabinoids. Analysis involving animal models carried out a variety of experiments. The results suggest that CBD exhibited antidepressant and anxiety effects in the animal models. This receptor is involved in the regulation of processes such as addiction, anxiety, appetite, nausea, sleep, vomiting, and pain perception.

    Hippocampus is a fundamental part of the brain that plays a significant role in various functions of the brain. Brain scans of individuals suffering from anxiety and depression frequently reveal a smaller hippocampus.

    Successful treatment of the condition is connected with the birth of new neurons in the hippocampus. Another animal study using mice revealed that repeated administration of CBD enhances regeneration of neurons from the hippocampus.

    This could be helpful for treating depression or anxiety. This is a significant aspect since evidence suggests that critically impaired neuronal plasticity influences suicidal behavior. Some products will be labeled with concentrations of CBD, others will have nutritional information.

    Products extracted using different methods may contain cannabinoids including THC, pesticides, and fungi that are left over from the plants.

    They could also contain material as well as other contaminants introduced during the manufacturing process. Nordic Oil provides high quality, full spectrum CBD oil products that are tested and certified third-party independent laboratories. Our products are tested for concentration, quality, and content. Our products provide in-depth information regarding the nature of the testing and results. Talk to your healthcare provider on the usage of CBD oil to treat your anxiety disorder.

    Let them explain to you whether CBD could bring about any undesired reactions. Should you experience any side effects, you should share these with your health care provider as well. Remember that everybody is different. CBD may take less time for some and more time for others to be effective.

    Follow instructions on the label cautiously and any directions provided to you by your doctor for best results. These reviews are from people using CBD oil for anxiety. Multiple studies indicate that CBD helped to relieve tension among individuals suffering from anxiety-related disorders. From the reviews and testimonials below, some former anxiety sufferers acquired almost instant results using Nordic oil CBD.

    A few others took weeks for their bodies to accumulate the levels of CBD required to have the positive impact. Like any devastating illness, it can be somewhat life-changing once it is finally relieved. Here are the samples of the reviews from real people. This stuff enabled to get through my day and sleep during the night. My anxiety, migraine, sleep problems and general stress-related issues have reduced significantly.

    I suffer from anxiety, RA, and fibromyalgia. However, I felt it is the right time to share my testimony and maybe help some else. When I was grieving the passing on of my son, I went through the most unpleasant anxiety attacks and severe depression. For quite long, I never left my house, the thought of leaving or driving left me so anxious, just in a panic mood. I would just be seated watching tv, and I would experience an awful panic attack. I thought I was dying. It was all anxiety.

    Many a time I called the paramedics. The information made available on this page is based on studies and research as well as experiences from CBD users.

    CBD For Anxiety

    Rodent analysis of CBD in stress and anxiety reveal that low-to-moderate dose of CBD has. Cannabidiol (CBD), the main non-psychotomimetic component of the plant of hippocampal neurogenesis promotes anxiety-related behaviours (Revest et al., . vehicle-treated mice;+p stressed mice (analysis of. “We showed that CBD increased animal's resilience in stress models of depressive disorder: a systematic review and network meta-analysis.




    Rodent analysis of CBD in stress and anxiety reveal that low-to-moderate dose of CBD has.

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