Hot Plate Research Articles

Investigating the Bioactive Potential of Persicaria hydropiper: GC-MS Profiling and In vivo Exploration of Antinociceptive and Antidiarrheal Effects

Aims: This study aimed to investigate the impact of methanol-derived leaf extracts from the Persicaria hydropiper plant on the GCMS analysis and in-vivo antinociceptive and antidiarrheal activities.
 Study Design: The GCMS analysis was used to analyze the phytochemicals of the methanolic extract of Persicaria hydropiper (MEPH). The research aimed to investigate the possible in-vivo activities, including the antinociceptive and antidiarrheal activity, of the plant's chemical ingredient, which is of pharmaceutical significance. Whether the changes seen in experimental animals have statistical significance.
 Methodology: Potential antinociceptive and antidiarrheal properties of MEPH were studied after phytochemicals were found by GCMS analysis of the plant. Swiss albino mice assessed antidiarrheal activity using the castor oil-induced method and antinociceptive activities at various dosages using the hotplate and glutamate-induced nociception methods, respectively.
 Results: The MEPH GCMS analysis revealed that 65 phytochemicals were found which have greater pharmacological activities. In contrast, MEPH inhibited peripheral nociception in the glutamate-induced paw licking nociceptive paradigm with percent inhibitions of 86.53 and 93.59, respectively. In addition, the hot plate test revealed a significant antinociceptive effect. Where the castor oil-induced antidiarrheal method showed 80.16 and 87% of inhibition of diarrhea compared to the standard loperamide's value of 84.19%. Each pharmacological model was experimented using the dose of 200 and 400 mg/kg.Conclusion: Several pathological conditions, including dysentery, Persistent diarrhea, arthritis and other pain, inflammation related diseases, may benefit in the future from the use of plant-derived pharmacological agents due to their antinociceptive and antidiarrheal activities.

Isolation, invitro, invivo anti-inflammatory, analgesic and antioxidant potential of Habenaria plantegania Lindl.

Habenaira plantaginea belong to orchid family which is native to Asia. Members of this family are commonly famous for the cure of pain and inflammation. To date, no research was found on isolation of compounds from this plant for the treatment of inflammation and analgesia nor has been published to our knowledge. The purpose of this study was to evaluate an analgesic, anti-inflammatory and anti-oxidant activity of the isolated compound from the most potent chloroform sub-fraction and the isolated compounds form the habenaria plantaginea. Anti-inflammatory analgesic and antioxidant potential of the various chloroform sub-fractions and isolated compounds from the most potent sub-fraction (HP-1 & HP-1) were screened for their in vitro enzymatic assays. Furthermore, prior to in-vivo investigation, the isolated compounds were subjected for their toxicity study. The potent compound was then examined for acetic acid-induced writhing, hot plate test, carrageenan-induced inflammation assays. Further various phlogistic agents were used for the evaluation of mechanism. In the COX-2 inhibitory assay the chloroform sub fraction Cf-4 demonstrated excellent activity as compared to the other sub-fraction with 92.15% inhibition. The COX-2 enzyme make prostaglandins which are directly involved in inflammation. Likewise against 5-LOX the Cf-4 was the most potent sub-fraction with IC50 3.77µg/mL. The 5-LOX catalyzes the biosynthesis of leukotrienes which is a group of lipid mediators of inflammation derived from arachidonic acid. Free radicals can induce inflammation through cellular damage while chronic inflammation generates a large number of free radicals, whose eventually lead toinflammation. In antioxidant assays the Cf-4 fraction was displayed excellent results against ABTS, DPPH and H2O2 free radical with 88.88, 77.44, and 65.52% inhibition at highest concentration. Likewise, the compound HP-1 demonstrated 88.81, 89.34 and 80.43% inhibition while compound HP-2 displayed 84.34, 91.52 and 82.34% inhibition against ABTS, DPPH and H2O2 free radical which were comparable to the standard drug ascorbic acid respectively. This study's findings validate the use of this species as traditional use.

Assessing effects of tamoxifen on tolerance, dependence, and glutamate and glutamine levels in frontal cortex and hippocampus in chronic morphine treatment

Tamoxifen has been shown to reduce glutamate release from presynaptic glutamatergic nerves and reverse tolerance to morphine-induced respiratory depression. Changes in glutamatergic neurotransmission in the central nervous system contribute to morphine tolerance, dependence, and withdrawal. This study, therefore, evaluated effects of tamoxifen on development of analgesic tolerance and dependence, and brain glutamate and glutamine levels in chronic morphine administration. Mice implanted with placebo or morphine pellets were injected with tamoxifen (0.6–2 mg/kg) or vehicle twice daily for 3 days. Nociceptive response was evaluated in the hot plate and tail immersion tests, 4, 48 and 72 h post-implant, and following a challenge dose of morphine (10 mg/kg). Withdrawal signs were determined after naloxone (1 mg/kg) administration. Morphine increased nociceptive threshold which declined over time. At 72 h, acute morphine elicited tolerance to the analgesic effect in the hot plate test in vehicle or tamoxifen administered animals. In the tail immersion test, however, tolerance to morphine analgesia was observed in tamoxifen, but not vehicle, co-administration. Tamoxifen did not reduce withdrawal signs. In contrast to previous reports, glutamate and glutamine levels in the hippocampus and frontal cortex did not change in the morphine-vehicle group. Confirming previous findings, tamoxifen (2 mg/kg) decreased glutamate and glutamine concentrations in the hippocampus in animals with placebo pellets. Both doses of tamoxifen significantly changed glutamate and/or glutamine concentrations in both regions in morphine pellet implanted animals. These results suggest that tamoxifen has no effect on dependence but may facilitate tolerance development to the antinociception, possibly mediated at the spinal level, in chronic morphine administration.

In vitro, invivo metabolism and quantification of the novel synthetic opioid N-piperidinyl etonitazene (etonitazepipne).

N-piperidinyl etonitazene (etonitazepipne) is a newly synthesized opioid related to the 2-benzylbenzimidazole analog class. Etonitazepipne has been formally notified and placed under intensive monitoring in Europe in January 2022. Nitazenes have high affinity at µ-opioid receptor (MOR). Etonitazepipne, specifically shows a EC50 of 2.49 nM, suggesting about 50 times higher potency combined with higher efficacy compared to morphine. Antinociceptive potency l ('hot plate test' with rats) was 192-fold greater than that of morphine. Here we report on a post-mortem case involving etonitazepipne and its quantification using a standard addition method (SAM) through liquid chromatography tandem mass spectrometry (LC-MS/MS). In addition, characterization and identification of phase I human metabolites using invitro assay based on pooled human liver microsomes (pHLM) was performed along with the analysis of authentic urine samples by means of high-performance liquid chromatography high-resolution tandem mass spectrometry (LC-HRMS/MS). The concentration of etonitazepipne in post-mortem blood and urine was 8.3 and 11 ng/mL, respectively. SAM was validated by assessing the following parameters: intraday and interday repeatability, matrix effect and recovery rate in post-mortem blood. A total of 20 and 14 metabolites were identified after pHLM incubation and urine analysis, respectively. Most pronounced invitro and invivo transformations were O-deethylation, hydroxylation, ketone reduction, and combinations thereof. Considering small traces of the parent drug often found in real cases, the identification of metabolic biomarkers is crucial to identify exposure to this drug. O-deethylated, oxidated metabolites, and combination thereof are proposed as urinary biomarkers along with the parent compound.

Evaluation of the Modulatory Effects of Capsicum Chinensis Methanol Extract in Streptozotocin-Induced Diabetic Neuropathic Pain in Mice

Diabetes is one of the common causes of neuropathic pain. The first-line treatment drugs used in alleviating neuropathic pain can cause adverse effects. Therefore, the aim of this study is to evaluate the analgesic property of Capsicum chinensis, since the plant was reported to be used against chronic pain in traditional medicine. Streptozotocin-induced diabetes was adopted to model neuropathy in mice and the antihyperalgesic effect of the extract was evaluated using a hot plate test, cold allodynia test, and Randall- Selitto paw pressure test. The plasma level of pain-associated inflammatory biomarkers like interleukin-6 (IL-6) and tissue necrotic factor-α (TNF-α) was also measured. Treatment with varying doses of extract (1, 2.5, and 5 mg/kg) significantly (p < 0.05) increased the mean reaction time to thermal pain during hot and cold plate tests. During the Paw pressure test, reaction time was significantly prolonged in the treatment groups and the plasma level of TNF-α and IL-6 were reduced (p < 0.05). The extract showed a better antihyperalgesic effect than the positive control drug (gabapentin). The result obtained showed that Capsicum chinensis extract can alleviate diabetes neuropathic pain in mice models with a better analgesic effect thanthe control drug (gabapentin).

RP–UHPLC–ESI–QTOF–MSn analyses, antioxidant, antimicrobial, analgesic activities and toxicity of Achillea ligustica All

Fourty five polyphenols were identified in the hydroethanol extract of Achillea ligustica All. by LC-HRMS/MS with caffeoyl-6-oleside (5.74%), eucommin A (4.03%), quercetin-3-O-β-D-glucoside (3.13%) and cirsimaritin (2.95%) as the major compounds. A good antioxidant potential was shown in DPPH, ABTS and phenanthroline tests and the highest antioxidant activity (A0.5:36.23 ± 3.07 μg/mL), which was close to the standard α-tocopherol, was shown in Reducing power. The extract inhibited the growth of all tested microorganisms with MICs ranging between 10 and 190 μg/mL. In the acute toxicity test, no death was observed at doses of 100, 750 and 1500 mg/Kg with DL50 higher than 2000 mg/Kg. In analgesic in vivo assay, the extract showed a very important capacity to reduce pain, whether central or peripheral, with a certain dose-dependent relationship. For the three tests (tail flick, hot plate and acetic acid assay), the effective dose was 750 mg/kg.

Anti-inflammatory, analgesic, antitussive and antipyretic activities of polyphenol-enriched fraction from Nymphaea candida

Ethnopharmacological relevance“Snow-white waterlily” (Nymphaea candida) dried flower possesses various efficacy in Uighur medicine such as reducing fever and nourishing the liver, anti-inflammatory and cough relieving, moistening the throat and quenching thirst. Aim of the studyPolyphenols are characteristic component of N. candida as well as its quality markers, and the purpose of this study was to conduct investigations into anti-inflammatory, antitussive, antipyretic, and analgesic activities of the polyphenol-enriched fraction from N. candida (NCTP) in order to validate the traditional efficacy of this plant. Materials and methodsThe polyphenols in NCTP were analyzed by HPLC, and an acute oral toxicity study was conducted for NCTP. The anti-inflammatory activities of NCTP were evaluated using xylene induced ear edema, capillary permeability, cotton pellet granuloma, and carrageenan-induced rat paw edema, of which multiple biochemical indices were measured in carrageenan-induced rat paw edema such as prostaglandin E2 (PGE2), cyclooxygenase-2 (COX-2),5-lipoxygenase (5-LOX), interleukin-6 (IL-6), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione (GSH) activities; the analgesic activities were investigated using acetic acid writhing, hot plate test, and formalin test; the anti-tussive and antipyretic effects were tested by ammonia induced cough in mice and yeast-induced fever respectively. ResultsNCTP with LD50 of 5222 mg/kg was low toxicity and safety. NCTP (200 mg/kg) could significantly reduce ear swelling and capillary permeability by 30.63% and 31.37%, respectively. NCTP revealed 15.76% inhibiting activities in cotton pellet granuloma in mice at a dosage of 200 mg/kg. Furthermore, NCTP (50, 100, and 200 mg/kg) substantially decreased carrageenin-induced paw edema in rats between 1 and 5 h, and NCTP could decrease PGE2, 5-LOX, COX-2 levels as well as IL-6, IL-1β, TNF-α activities compared with the control group; NCTP could decrease MDA contents in carrageenin-induced rise, and increase SOD and GSH activities. Furthermore, the dose-dependent inhibition effect of NCTP on pain was revealed in the hot plate experiment. In addition to reducing the amount of writhes brought on by acetic acid, NCTP (50, 100, and 200 mg/kg) significantly inhibited pain latency against both stages of the formalin test. Moreover, NCTP (50, 100, 200 mg/kg) showed the better antitussive activities in mice in a dose-dependent manner. In the yeast-induced pyrexia test, dosages of 50, 100, and 200 mg/kg resulted in a statistically significant drop in rectal temperature. ConclusionThe experimental results proved the analgesic, anti-inflammatory, anti-tussive and antipyretic activities of the polyphenol-enriched fraction from N. candida, and supported the traditional use of this plant as well.

The Effect of Ethanoic Extract of Xylopiaaethiopica (UDA) on Pain Sensitivity of Female Wistar Rats

Background: In African traditional medicine, the dried pods of Xylopia aethiopica are frequently used to managedifferent human ailments. In Nigeria, it is consumed in soups after childbirth to aid in wound healing, painrelief, uterine recovery, and lactation. The study investigates the impact of Xylopia aethiopicafruit extract on painsensitivity using Wistar rats.Methods: Twelve female Wistar rats were divided into two groups (Group 1 - Control and Group 2 -100mg/kgXylopia aethiopicaextract-fed) and received standard rat chow and water for fourteen days following which painsensitivity was assessed using a hot plate. The results were presented as Mean and Independent Student T-testwas utilized for statistical analysis with significance determined at P≤0.05. Increased pain tolerance indicatedreduced sensitivity.The escape latencies of both groups were 5secs and 8 secs respectively. Group 2 demonstrated a noteworthyincrease in pain tolerance compared to Group 1 (P = 0.003). This experimental study indicates that the ethanoicextract of Xylopia aethiopicafruit has analgesic properties.Conclusion: The result of this study provides support for the use of dried Xylopia aethiopicapods in painmanagement across some communities in Southern Nigeria.

The Effect of Blended Palm Oil Biodiesel Droplet Properties on Evaporation Characteristics

The evaporation characteristics of a single fuel droplet of diesel fuel (DF) and the Malaysian palm oil biodiesel-diesel blend (B10-B50) were studied experimentally. The fuel droplet properties consisted of different ratios of palm oil biodiesel mixtures which could influence the droplet behaviour when impinged on the heated surface. By employing the hot surface deposition test (HSDT) method, the droplets impinging on the heated surface of an aluminum alloy plate were observed to evaluate the droplet's evaporation characteristics including the evaporation lifetime and maximum evaporation point (MEP) of the tested fuels. Furthermore, the deposit’s surface temperature for dry condition (timp=7 seconds) and wet condition (timp=3 seconds) test were also measured during the deposition test. Finally, the deposit development on the heated surface was evaluated through a logarithmic expression of MR/mD = αNDβ. The results showed that the evaporation lifetime of each test fuel decreased with increasing hot plate surface temperature. Furthermore, the MEP was the highest for B30 (380°C), followed by B20 and B40 (375°C), B10 and B50 (365°C), and DF (360°C). In the dry condition test, the recorded average minimum and maximum deposit surface temperatures were observed to be within the range of Td=295°C to Td=325°C for DF and Td=290°C to Td=350°C for B10-B50 fuels. On the other hand, for the wet condition test, the recorded average minimum deposit surface temperatures for both DF and B10-B50 fuels were consistently lower than the hot plate temperature. DF exhibited the most variation, ranging from Td=200°C to Td=300°C, whereas, for B10-B50, the recorded deposit surface temperature was only ranging from Td=150°C to Td=200°C.

Desulfurisasi Batubara Dengan Metode Leaching Menggunakan Naoh Dan HCL Di PT. Anugerah Krida Utama, Kutai Kartanegara, Kalimantan Timur

The utilization of coal as a fossil fuel causes several ecological problems, as for the consequences of the coal combustion process, namely pollution and emissions. Combustion of high sulfur coal produces sulfur dioxide gas (SO2). This sulfur dioxide (SO2) will become H2SO4 (sulfuric acid) which can directly or indirectly disrupt human life, such as causing acid rain, causing tightness in the respiratory tract and causing corrosion and shortening the life of factory equipment. To reduce SO2 gas, a reduction in sulfur content is carried out before combustion which is called desulfurization. This research was conducted using the leaching method with variations in leaching agent and solution concentration. Leaching agents used in this study are NaOH and HCl. The coal to be desulfurized is coal from PT Anugerah Krida Utama with an initial total sulfur content of 4,05% adb. 10 grams of coal with a size of 0,212 mm was leached with 250 ml of chemical solution using a hot plate stirrer at 80˚C and 250 rpm for 1 hour. The results showed that the optimum condition for leaching agent NaOH occurred at a concentration of 8 M showing the initial total sulfur content of 4,05% adb decreased to 1,69% adb with a maximum percentage decrease of 58,27% and at leaching agent HCl the optimum condition occurred at a concentration of 1 M showing the initial total sulfur content of 4,05% adb decreased to 2,91% adb with a maximum percentage decrease of 28,14%.

A Novel Leu-Enkephalin Prodrug Produces Pain-Relieving and Antidepressant Effects.

Persistent pain is a significant healthcare problem with limited treatment options. The high incidence of comorbid chronic pain and depression significantly reduces life quality and complicates the treatment of both conditions. Antidepressants are less effective for pain and depression than for depression alone and they induce severe side effects. Opioids are highly efficacious analgesics, but rapid development of tolerance, dependence, and debilitating side effects limit their efficacy and safe use. Leucine-enkephalin (Leu-ENK), the endogenous delta opioid receptor agonist, controls pain and mood and produces potent analgesia with reduced adverse effects compared to conventional opioids. High proteolytic instability, however, makes Leu-ENK ineffective after systemic administration and limits its clinical usefulness. KK-103, a Leu-ENK prodrug, was developed to overcome these limitations of Leu-ENK via markedly increased plasma stability in mice. We showed rapid and substantially increased systemic adsorption and blood plasma exposure of KK-103 compared to Leu-ENK. We also observed brain uptake of radiolabeled KK-103 after systemic administration, indicating a central effect of KK-103. We then established KK-103's prolonged antinociceptive efficacy in the ramped hot plate and formalin test. In both models, KK-103 produced a comparable dose to the maximum antinociceptive-effect relationship. The pain-alleviating effect of KK-103 primarily resulted from activating the delta opioid receptor after the likely conversion of KK-103 to Leu-ENK in vivo. Finally, KK-103 produced an antidepressant-like activity comparable to the antidepressant desipramine, but with minimal gastrointestinal inhibition and no incidence of sedation.

Biphenyl-rGO composite room temperature gas sensor for enhanced amine sensing

Amines, which are classified as volatile organic compounds (VOCs), serve a variety of purposes in the fields of environmental monitoring, food safety, and healthcare diagnosis. The present technique for detecting amine levels involves sophisticated setups and bulky equipment. Here. In this study, a chemoresistive gas sensor is developed that is cost-effective and easy to operate at room temperature (RT). The sensor is designed specifically for the detection of Ammonia, dimethylamine (DMA), trimethylamine (TMA), and total volatile basic nitrogen (TVB-N). Using biphenyl-reduced graphene oxide (B-rGO) composite gas sensors effectively addresses the issues of low sensitivity-selectivity and long-term instability commonly observed in conventional amine sensors. B-rGO sensor produced sensitivity of ∼3500 and selectivity above 30 for TVB-N sensing. The sensor is stable for temperature fluctuations below 50 °C and shows stable sensing response for period of over 3 months. A Chemoresistive B-rGO sensor was developed using an ultrasonic spray deposition system with optimized flow rate of 50 mL/h. Rapid evaporation of solvent using hot plate has resulted in unique morphology for B-rGO film sensors. The highest sensitivity, ∼836, is obtained for 100 ppm of ammonia with ammonia > DMA > TMA as a sensitivity order. B-rGO showed almost seven times higher amine sensitivity than rGO which highlights the importance of biphenyl in the B-rGO composite. Sensor calibration curve has been presented in the study to understand change in the sensitivity of sensor with increasing analyte gas concentration. The calibration curve has an average R-squared value of 0.98.

The preferential effect of Clemastine on F3/Contactin-1/Notch-1 compared to Jagged-1/Notch-1 justifies its remyelinating effect in an experimental model of multiple sclerosis in rats

Clemastine (CLM) is repurposed to enhance remyelination in multiple sclerosis (MS) patients. CLM blocks histamine and muscarinic receptors as negative regulators to oligodendrocyte differentiation. These receptors are linked to the canonical and non-canonical Notch-1 signaling via specific ligands; Jagged-1 and F3/Contactin-1, respectively. Yet, there are no previous studies showing the influence of CLM on Notch entities. Herein, the study aimed to investigate to which extent CLM aligns to one of the two Notch-1 arms in experimental autoimmune encephalomyelitis (EAE) rat model. Three groups were utilized where first group received vehicles. The second group was injected by spinal cord homogenate mixed with complete Freund’s adjuvant on days 0 and 7. In the third group, CLM (5 mg/kg/day; p.o) was administered for 15 days starting from the day of the first immunization. CLM ameliorated EAE-associated motor and gripping impairment in rotarod, open-field, and grip strength arena beside sensory anomalies in hot plate, cold allodynia, and mechanical Randall-Selitto tests. Additionally, CLM alleviated depressive mood observed in tail suspension test. These findings harmonized with histopathological examinations of Luxol-fast blue stain together with enhanced immunostaining of myelin basic protein and oligodendrocyte lineage gene 2 in corpus callosum and spinal cord. Additionally, CLM enhanced oligodendrocyte myelination and maturation by increasing 2′,3′-cyclic nucleotide 3′-phosphodiesterase, proteolipid protein, aspartoacylase as well. CLM restored the level of F3/Contactin-1 in the diseased rats over Jagged-1 level; the ligand of the canonical pathway. This was accompanied by elevated gene expression of Deltex-1 and reduced hairy and enhancer-of-split homologs 1 and 5. Additionally, CLM suppressed microglial and astrocyte activation via reducing the expression of ionized calcium-binding adaptor molecule-1 as well as glial fibrillary acidic protein, respectively. These results outlined the remyelinating beneficence of CLM which could be due to augmenting the non-canonical Notch-1 signaling over the canonical one.

In-vivo Pharmacological Evaluation of Analgesic Activity of Ethanolic Extract of Doronicum hookeri Clarke Rhizomes in Wistar Rats

A number of plants are used traditionally in different medical conditions by practitioners of traditional medicines but their claim is not yet evaluated scientifically in laboratory animals. Based on the ethnomedical claims made by the Unani health practitioners, the Clarke rhizomes of Doronicum Hookeri was evaluated for analgesics activity in rats to confirm its claim. The successive plant extraction was carried out using Soxhlet apparatus by employing ethanol as a solvent of the dried rhizomes of Doronicum Hookeri. The % yield of extracted compound was 28.27% w/w. The qualitative preliminary phytochemical screening revealed the presence of alkaloids, saponins, tannins, flavonoids, glycosides, phenolic content, terpenoids and volatile oils in the rhizomes of ethanolic extract of D. Hookeri. The extract was orally administered in rats at low dose and high dose (200 mg/kg, 400 mg/kg) and was evaluated using Eddy’s Hot Plate Method in rats for analgesics activity. Diclofenac sodium (50 mg/kg) and was taken as a standard drug. The maximum possible analgesia % of ethanolic extract of rhizomes of D. Hookeri were found to be highest at a dose of 400mg/kg which showed 68.95% and 80% analgesia at 45 minute and 60 minute which when compared to Diclofenac sodium showed 73.28% and 85.71% at 45 minute and 60 minutes. The analgesic efficacy of ethanolic extract of rhizomes of D. Hookeri showed significant analgesic activity (p<0.04) in dose dependent manner at different time intervals of 0, 15, 30, 45 and 60 min. This asserts ethnomedical claims of some tribes regarding the analgesic activity of this plant.
 Keywords - Analgesics, eddy’s hot plate, D. Hookeri, Diclofenac sodium.

Supernova emission of secretly interacting neutrino fluid: Theoretical foundations

Neutrino-neutrino scattering could have a large secret component that would turn neutrinos within a supernova (SN) core into a self-coupled fluid. Neutrino transport within the SN core, emission from its surface, expansion into space, and the flux spectrum and time structure at Earth might all be affected. We examine these questions from first principles. First, diffusive transport differs only by a modified spectral average of the interaction rate. We next study the fluid energy transfer between a hot and a cold blackbody surface in plane-parallel and spherical geometry. The key element is the decoupling process within the radiating bodies, which themselves are taken to be isothermal. For a zero-temperature cold plate, mimicking radiation into free space by the hot plate, the energy flux is 3%–4% smaller than the usual Stefan-Boltzmann law. The fluid energy density just outside the hot plate is numerically 0.70 of the standard case, the outflow velocity is the speed of sound vs=c/3, conspiring to a nearly unchanged energy flux. Our results provide the crucial boundary condition for the expansion of the self-interacting fluid into space, assuming an isothermal neutrino sphere. We also derive a dynamical solution, assuming the emission suddenly begins at some instant. A neutrino front expands in space with luminal speed, whereas the outflow velocity at the radiating surface asymptotically approaches vs from above. Asymptotically, one thus recovers the steady-state emission found in the two-plate model. A sudden end to neutrino emission leads to a fireball with constant thickness equal to the duration of neutrino emission. Published by the American Physical Society 2024

Investigation of elemental composition in red teff grains using inductively coupled plasma optical emission spectroscopy (ICP OES), Sire District, Arsi zone, Ethiopia

BackgroundMinerals are important not only for better plant growth and development but also for human and animal nutrition. It is known that east and west Gojam in the Amhara region and east and west Shoa areas in the Oromia region Ethiopia's most teff growing areas. However, there is no information on the mineral content and nutritional worth of Teff Sire district, Arsi zone, Ethiopia. Since ICP OES is a powerful technique to examine elemental compositions even in lower concentration, it is used in this work to investigate the elemental composition of red teff samples. MethodsThe elemental compositions of red Teff grain samples were determined using ICP-OES from three sites: S1, S2, and S3 of Sire district, Arsi zone, Ethiopia. Wet digestion of the teff samples was carried out by weighing 0.5 g red teff sample and digested with 8 ml HNO3 and 2 ml H2O2 (30%) for 3:00 h at a temperature of 100℃ on hot plate. The investigations of method validation, limit of detection and limit of quantification were also carried out. ResultsThe average amount of elements in red teff sample obtained as 172–280 mg/kg Fe, 13–76 mg/kg Mn, 8.2–8.5 mg/kg Cu, 24–26 mg/kg Zn, and toxic trace elements 0.12–0.29 mg/kg Pb and 0.15–0.22 mg/kg Cd. The limit of detection found in ranges from 0.21 mg Kg−1 to 10.44 mg Kg−1 whereas quantification limit resulted in 0.7 mg Kg−1 to 34.8 mg Kg−1 for the metals under consideration. The method was validated by its linear range in the concentration range of 0.028–1.4 ppm or 0.056–2.8 ppm and excellent recovery result was achieved in the range of 90–120%. ConclusionThis study aimed to investigate the mineral content in red teff cultivated in Ethiopia specifically Arsi zone by using ICP OES. From the obtained results, Iron was the first abundant essential element in red teff compared to Mn, Cu and Zn. The level of trace elements: Cd and Pb in the samples slightly above the acceptable limit, possibly due to agricultural practices like usage of fertilizers, pesticides, and other industrial products. Overall, this red teff elemental composition information contributes to the nutrition database and food safety in Ethiopia and beyond.

The Toxicological and Pharmacological Evaluation of the Anacyclus pyrethrum Aqueous Extract: Implications for Medicinal and Therapeutic Applications

Plants have long been valued for their medicinal and nutritional contributions to human life. Anacyclus pyrethrum, a member of the Asteraceae family, has attracted increasing attention as a source of natural products with diverse applications. In this study, we explored the toxicity and pharmacological properties of the aqueous extract of A. pyrethrum (AEAP). The acute toxicity study involved groups of mice subjected to oral administration of varying doses of AEAP, with immediate post-administration observations to detect any signs of toxicity or mortality. Comprehensive biochemical and hematological analyses encompassed assessments of renal function. The pharmacological profile was assessed by evaluating antinociceptive, anxiolytic, and antidepressant effects, which were measured using the hot plate test, elevated plus maze, open field test, and forced swim test, respectively. Different doses (100, 200, 400, and 800 mg/kg) were administered to rats via gavage for this assessment. The results revealed that the acute toxicity demonstrated the safety of AEAP at the tested doses, with no observed mortality or significant alterations. Moreover, it revealed that AEAP possesses an LD50 value greater than 5000 mg/kg. The pharmacological properties of AEAP demonstrated anxiolytic and antidepressant activities at a dose of 200 mg/kg, while no antinociceptive effect was observed. These findings underscore the potential of A. pyrethrum as a natural source of bioactive compounds with therapeutic applications. Further research is needed to explore long-term and chronic effects for a comprehensive assessment.

Effect of different roasting methods on clove bud extracted oil

This research aims to study the effect of hotplate and microwave roasting at different time,temperature/power on extracted clove bud oil.In this study, oils extracted from clove buds were subjected to hotplate roasting at different times (10, 20, and 15 min) and temperatures (80,100, and 1800 C) and microwave roasting at different power levels (450, 600, 840 W) and time (30 s and 1 min) were evaluated. Physical property parameters color, density, and refractive index; and chemical quality parameters antioxidant properties, chemical composition analysis, functional group analysis, and antimicrobial activity were carried out.Analysis showed that under these conditions there was change in the yield of oil, chemical composition in the spice.The antioxidant properties, chemical composition, antimicrobial activities, and presence of functional groups in clove bud oil increased with microwave power and time up to 600 W and 1 min, for hot plate roasting at 180oC and 10 min, respectively. Based on these findings, roasting clove buds in the microwave with moderate power and short treatment times might be a feasible choice. Both roasting processes may generate new compounds as natural food preservatives

Microglia TREM1-mediated neuroinflammation contributes to central sensitization via the NF-κB pathway in a chronic migraine model

BackgroundNeuroinflammation, mediated by the activation of microglia, contributes to central sensitization, which is associated with the development of chronic migraine (CM). TREM1 receptors amplify the inflammatory response. However, their relationship to CM is unclear. Thus, this study endeavoured to elucidate the exact role of TREM1 in CM.MethodsNitroglycerin (NTG) was repeatedly administered intraperitoneally to establish the CM model. Mechanical and thermal sensitivities were assessed using von Frey filaments and hot plate assays. Using Western blotting, TREM1, NF-κB pathway, NLRP3 inflammasome components, and proinflammatory cytokines were all detected. Immunofluorescence was used to examine the cellular distribution of TREM1 and NLRP3, the number of microglia, immunoreactivity, and morphological changes. We examined the effects of TREM1 antagonists (LR12) and NF-κB inhibitors (PDTC) on pain behaviour, as well as the production of c-fos and CGRP. Additionally, we investigated whether LR12 and PDTC affect the activation of microglia and the NLRP3 inflammasome. We synthesized siRNA and TREM1-overexpressing plasmids to transfect BV2 cells treated with LPS and normal BV2 cells and treated TREM1-overexpressing BV2 cells with PDTC. The NF-κB pathway, NLRP3 inflammasome components, and proinflammatory cytokines were quantified using Western blotting.ResultsFollowing NTG administration, the expression of TREM1 was significantly upregulated and exclusively localized in microglia in the TNC, and was well co-localized with NLRP3. Furthermore, activation of the classical NF-κB pathway was observed. Pre-treatment with LR12 and PDTC effectively attenuated mechanical hypersensitivity, suppressed the expression of c-fos and CGRP, and inhibited NF-κB activity in CM mice. Additionally, inhibition of TREM1 and NF-κB activity mitigated NTG-induced microglia and NLRP3 activation, as well as proinflammatory cytokines production. In vitro, knockdown of TREM1 resulted in attenuated activation of the NF-κB pathway following lipopolysaccharide (LPS) treatment and reduced expression of NLRP3 inflammasome components as well as proinflammatory cytokines. After TREM1 overexpression, the NF-κB pathway was activated, NLRP3 inflammasome components and proinflammatory cytokines were upregulated, and PDTC reversed this phenomenon.ConclusionsOur findings suggest that TREM1 regulates microglia and NLRP3 activation via the NF-κB pathway, thereby contributing to central sensitization and implicating its involvement in chronic migraine pathogenesis.

Lidocaine-Liposomes-A Promising Frontier for Transdermal Pain Management.

(1) Background: We aim to develop novel gel formulations for transdermal drug delivery systems in acute and inflammatory pain therapy. (2) Methods: We induced inflammation by the injection of λ-carrageenan on the hind paw of 80 Wistar male rats. The animals were randomized into eight groups of 10 rats each: C (placebo gel), E (EMLATM), L (lidocaine 2%), L-CD (lidocaine + cyclodextrin 2.5%), L-LP (lidocaine + liposomes 1.7%), L-CS (lidocaine + chitosan 4%), L-CSh (lidocaine + chitosan hydrochloride), and L-CS-LP (lidocaine + chitosan + liposomes). The behavior response was determined with a hot plate, cold plate, and algesimeter, each being performed at 30, 60, 120, 180, and 240 min after pain induction. At the end of the experiment, tissue samples were collected for histological assessment. (3) Results: L-LP had the greatest anesthetic effects, which was proven on the cold plate test compared to placebo and EMLATM (all p ≤ 0.001). L-CS-LP had a significant effect on cold plate evaluation compared to placebo (p ≤ 0.001) and on hot plate evaluation compared to EMLATM (p = 0.018). (4) Conclusions: L-LP is a new substance with a substantial analgesic effect demonstrated by the cold plate in the first 120 min. Further studies with more animals are needed to determine the maximum doses that can be applied for a better analgesia with minimum side effects.