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The knowledge of the physiological aspects of Caatinga's vegetal species is extremely important for preserving this biome, which suffers with human impacts, mainly to select propagation methods. Erythrina velutina is a Brazilian tree, generally found in Caatinga, with medical and forestry potential. The objective of this paper was to determine the best soaking period in gibberellin solution to achieve the highest germination and to evaluate the internal anatomy by digital microtomography of E. velutina seeds. The design was completely randomized and consisted of eight treatments: 1, 3, 6, 12, 24 and 48 h of soaking, scarified seeds and the control with no-scarified seeds. Digital microtomography was efficient in describing the anatomy of the seeds and distinguishing their tissues. There was no significant difference between the treatments at different soaking times, as the gibberellic acid did not influence the germination; only the control presented a lower germination percentage, differing from the other treatments. The study presents evidence that E. velutina seeds do not require the exogenous use of gibberellic acid, but only the scarification process. In addition, the use of digital microtomography can be useful in understanding the anatomy of seeds, especially forest species, which can contribute to the future studies of other plant species. [ABSTRACT FROM AUTHOR]

[Display omitted] Natural products of pharmaceutical interest often do not reach the drug market due to the associated low yields and difficult extraction. Knowledge of biosynthetic pathways is a key element in the development of biotechnological strategies for plant specialized metabolite production. Erythrina species are mainly used as central nervous system depressants in folk medicine and are important sources of bioactive tetracyclic benzylisoquinoline alkaloids (BIAs), which can act on several pathology-related biological targets. In this sense, in an unprecedented approach used with a non-model Fabaceae species grown in its unique arid natural habitat, a combined transcriptome and metabolome analyses (seeds and leaves) is presented. The Next Generation Sequencing-based transcriptome (de novo RNA sequencing) was carried out in a NextSeq 500 platform. Regarding metabolite profiling, the High-resolution Liquid Chromatography was coupled to DAD and a micrOTOF-QII mass spectrometer by using electrospray ionization (ESI) and Time of Flight (TOF) analyzer. The tandem MS/MS data were processed and analyzed through Molecular Networking approach. This detailed macro and micromolecular approach applied to seeds and leaves of E. velutina revealed 42 alkaloids, several of them unique. Based on the combined evidence, 24 gene candidates were put together in a putative pathway leading to the singular alkaloid diversity of this species. Overall, these results could contribute by indicating potential biotechnological targets for modulation of erythrina alkaloids biosynthesis as well as improve molecular databases with omic data from a non-model medicinal plant, and reveal an interesting chemical diversity of Erythrina BIA harvested in Caatinga. [ABSTRACT FROM AUTHOR]

Objectives: To study the effects of the standardized extract from the leaves of Erythrina velutina in behavioural and oxidative parameters in the ketamine‐induced schizophrenia model. Methods: Mice received ketamine (KET) or saline for 7 days. From 8th to 14th day, the animals received Erythrine (Eryt) (100, 200 or 400 mg/kg) or olanzapine (Olanz), 1 h after KET administration. At 14th day, 30 min after the last administration of KET, the open‐field and pre‐pulse inhibition (PPI) tests were performed. Then, the animals were sacrificed and the prefrontal cortex (PFC), hippocampus (HC) and striatum (ST) were dissected for the oxidative tests. Key findings: Ketamine increased spontaneous locomotor activity and grooming. KET decreased the PPI, which was reversed by combining it with Eryt or olanzapine. KET decreased GSH concentration in PFC and ST this was reversed by Eryt. KET increased MDA concentration in PFC and HC this was reversed by Eryt. Eryt and Olanzapine reduced MDA concentration in ST when compared to KET group. Nitrite concentration was reduced by administration of KET in the PFC. Conclusions: These results demonstrate that the standardized extract of E. velutina can prevent behavioural symptoms and oxidative stress induced by repeated doses of KET. [ABSTRACT FROM AUTHOR]

The objective of this study was to verify a possible neuroprotective effect of the ethanolic extract of Erythrina velutina (EEEV). Male Swiss mice were submitted to transient cerebral ischemia by occlusion of both carotid arteries for 30 min and treated for 5 days with EEEV (200 or 400 mg/kg) or Memantine (MEM) 10 mg/kg, with initiation of treatment 2 or 24 h after Ischemia. On the 6th day after the induction of ischemia, the animals were submitted to evaluation of locomotor activity and memory and then sacrificed. The brains were dissected for the removal of the prefrontal cortex (PFC), hippocampus (HC) and striatum (ST) for determination of amino acid concentrations. In the step down and Y-maze tests, ischemia caused damage to the animals and treatment with EEEV or MEM reversed this effect. The animals submitted to ischemia also showed memory deficit in the object recognition test, an effect that was reverted by EEEV400 and MEM10. Amino acid dosage showed an increase in excitatory amino acid concentrations in the PFC of the ischemic animals and this effect was reversed by the treatment with EEEV400/24H. Regarding the inhibitory amino acids, ischemia caused an increase of taurine in the PFC while treatment with MEM10/24H or EEEV400/24H reversed this effect. In HC, an increase in excitatory amino acids was also observed in ischemiated animals having treatment with EEEV200/2H or EEEV400/24H reversed this effect. Similar effect was also observed in the same area in relation to the inhibitory amino acids with treatment with MEM10/24H or EEEV400/24H. In the ST, ischemia was also able to cause an increase in excitatory amino acids that was reversed more efficiently by the treatments with MEM10/24H and EEEV200. Also in this area, an increase of taurine and GABA was observed and only the treatment with EEEV200/2H showed a reversion of this effect. In view of these findings, EEEV presents a neuroprotective effect possibly due to its action on amino acid concentrations, and is therefore a potential therapeutic tool in reducing the damage caused by ischemia. [ABSTRACT FROM AUTHOR]

Trypsin and chymotrypsin inhibitors from Erythrina velutina seeds have been previously isolated by our group. In previous studies using a sepsis model, we demonstrated the antitumor and anti-inflammatory action of these compounds. This study aimed to evaluate the gastroprotective and antielastase effects of protein inhibitors from E. velutina seeds in an experimental stress-induced ulcer model. Two protein isolates from E. velutina seeds, with antitrypsin (PIAT) and antichymotrypsin (PIAQ) activities, were tested. Both protein isolates showed a high affinity and inhibitory effect against human neutrophil elastase, with 84% and 85% inhibition, respectively. Gastric ulcer was induced using ethanol (99%) in 6 groups of animals (female Wistar rats, n = 6). Before ulcer induction, these animals were treated for 5 days with one of the following: (1) PIAT (0.2 mg·kg−1), (2) PIAT (0.4 mg·kg−1), (3) PIAQ (0.035 mg·kg−1), (4) ranitidine hydrochloride (50 mg·kg−1), (5) saline solution (0.9%), or (6) no intervention (sham). Both PIAT and PIAQ protected gastric mucosa, preventing hemorrhagic lesions, edema, and mucus loss. No histologic toxic effects of PIAT or PIAQ were seen in liver and pancreatic cells. Our results show that protein isolates from E. velutina seeds have potential gastroprotective effects, placing these compounds as natural candidates for gastric ulcer prevention. [ABSTRACT FROM AUTHOR]

Trypsin and chymotrypsin inhibitors from Erythrina velutina seeds have been previously isolated by our group. In previous studies using a sepsis model, we demonstrated the antitumor and anti-inflammatory action of these compounds. This study aimed to evaluate the gastroprotective and antielastase effects of protein inhibitors from E. velutina seeds in an experimental stress-induced ulcer model. Two protein isolates from E. velutina seeds, with antitrypsin (PIAT) and antichymotrypsin (PIAQ) activities, were tested. Both protein isolates showed a high affinity and inhibitory effect against human neutrophil elastase, with 84% and 85% inhibition, respectively. Gastric ulcer was induced using ethanol (99%) in 6 groups of animals (female Wistar rats, n = 6). Before ulcer induction, these animals were treated for 5 days with one of the following: (1) PIAT (0.2 mg·kg−1), (2) PIAT (0.4 mg·kg−1), (3) PIAQ (0.035 mg·kg−1), (4) ranitidine hydrochloride (50 mg·kg−1), (5) saline solution (0.9%), or (6) no intervention (sham). Both PIAT and PIAQ protected gastric mucosa, preventing hemorrhagic lesions, edema, and mucus loss. No histologic toxic effects of PIAT or PIAQ were seen in liver and pancreatic cells. Our results show that protein isolates from E. velutina seeds have potential gastroprotective effects, placing these compounds as natural candidates for gastric ulcer prevention. [ABSTRACT FROM AUTHOR]

Background: Erythrina velutina is a tree common in the northeast of Brazil extensively used by traditional medicine for the treatment of central nervous system disorders. Objective: To develop a standardized ethanol extract of E. velutina (EEEV) and to investigate the neuroprotective potential of the extract and rizonic acid (RA) from E. velutina on neuronal cells. Materials and methods: The plant drug of E. velutina previously characterized was used for the production of EEEV. Three methods were evaluated in order to obtain an extract with higher content of phenols. The neuroprotective effect of standardized EEEV (HPLC-PDA) and RA was investigated on SH-SY5Y cell exposure to the neurotoxin 6-hydroxydopamine (6-OHDA). Results: The powder of the plant drug was classified as moderately coarse and several quality control parameters were determined. EEEV produced by percolation gave the highest phenol content when related to others extractive methods, and its HPLC-PDA analysis allowed to identify four flavonoids and RA, some reported for the first time for the species. EEEV and RA reduced significantly the neurotoxicity induced by 6-OHDA in SH-SY5Y cells determined by the MTT assay and the nitrite concentration. EEEV also showed a free radical scavenging activity. Conclusion: This is the first pharmacological study about E. velutina which used a controlled standardized extract since the preparation of the herbal drug. This extract and RA, acting as an antioxidant, presents a neuroprotective effect suggesting that they have potential for future development as a therapeutic agent in neurodegenerative disease as Parkinson. [ABSTRACT FROM AUTHOR]

The aim of this study was to evaluate the effect of different abiotic stresses on the activity of antioxidant enzymes and on accumulation of proline in Erythrina velutina Willd. seeds during germination. Mulungu seeds were scarified and placed to germinate at constant temperatures of 15, 25, and 35 °C, moistened with distilled water, and exposed to 12 h of light. Other seeds were exposed to solutions of NaCl (EC of 0, 4, and 8 dS.m-1) and polyethylene glycol (osmotic potentials of 0.0, -0.2, and - 0.6 MPa) and maintained in a germination chamber set at 25 °C and 12 h photoperiod for seven days. At the end of each period of imbibition, the embryonic axis and cotyledons of the seedlings were collected separately and used to quantify proline content and the activity of antioxidant enzymes. These were detected in both the cotyledons and embryonic axis of the mulungu seeds. Antioxidant activity varied depending upon the type and degree of stress applied. It was concluded that under the aspect of the detoxification process, the mechanism found in mulungu seeds is more efficient when subjected to different temperatures followed by salt stress and water stress. [ABSTRACT FROM AUTHOR]

Objectives We studied the effects of ethyl acetate fraction ( EAcF) obtained from Erythrina velutina leaves on mammalian myocardium. Methods The effect of EAcF on the contractility was studied using guinea-pig left atria mounted in a tissue bath ( Tyrode's solution, 29° C, 95% CO2, 5% O2) and electrically stimulated (1 Hz). Concentration-response curves of EAcF were obtained in the presence of propranolol (1 μ m), nifedipine (1 μ m) and in reserpinized animals (5 mg/kg). The involvement of l-type calcium current ( ICa,L) on the EAcF effect was observed in cardiomyocytes of mice assessed using patch-clamp technique. Key findings EAcF (550 μg/ml) had a positive inotropic effect, increasing the atrial force by 164% ( EC50 = 157 ± 44 μg/ml, n = 6), but it was less potent than isoproterenol ( EC50 = 0.0036 ± 0.0019 μg/ml, n = 8). The response evoked by EAcF was abolished by propranolol or nifedipine. Reserpine did not alter the inotropic response of EAcF. Furthermore, an enhancement of the ICa,L peak (31.2%) with EAcF was observed. Chemical analysis of EAcF revealed the presence of at least 10 different flavonoid glycoside derivatives. Two were identified as vicenin II and isorhoifolin. Conclusions We conclude that EAcF increases the cardiac contractile force by increasing the l-type calcium current and activating the adrenergic receptor pathway. [ABSTRACT FROM AUTHOR]

Inhibitors of peptidases isolated from leguminous seeds have been studied for their pharmacological properties. The present study focused on purification, biochemical characterization and anti-inflammatory and anticoagulant evaluation of a novel Kunitz trypsin inhibitor from Erythrina velutina seeds (EvTI). Trypsin inhibitors were purified by ammonium sulfate (30–60%), fractionation followed by Trypsin-Sepharose affinity chromatography and reversed-phase high performance liquid chromatography. The purified inhibitor showed molecular mass of 19,210.48 Da. Furthermore, a second isoform with 19,228.16 Da was also observed. The inhibitor that showed highest trypsin specificity and enhanced recovery yield was named EvTI (P2) and was selected for further analysis. The EvTI peptide fragments, generated by trypsin and pepsin digestion, were further analyzed by MALDI-ToF-ToF mass spectrometry, allowing a partial primary structure elucidation. EvTI exhibited inhibitory activity against trypsin with IC50 of 2.2×10−8 mol.L−1 and constant inhibition (Ki) of 1.0×10−8 mol.L−1, by a non-competitive mechanism. In addition to inhibit the activity of trypsin, EvTI also inhibited factor Xa and neutrophil elastase, but do not inhibit thrombin, chymotrypsin or peptidase 3. EvTI was investigated for its anti-inflammatory and anti-coagulant properties. Firstly, EvTI showed no cytotoxic effect on human peripheral blood cells. Nevertheless, the inhibitor was able to prolong the clotting time in a dose-dependent manner by using in vitro and in vivo models. Due to anti-inflammatory and anticoagulant EvTI properties, two sepsis models were here challenged. EvTI inhibited leukocyte migration and specifically acted by inhibiting TNF-α release and stimulating IFN-α and IL-12 synthesis. The data presented clearly contribute to a better understanding of the use of Kunitz inhibitors in sepsis as a bioactive agent capable of interfering in blood coagulation and inflammation. [ABSTRACT FROM AUTHOR]

Analytical techniques have been used to characterize compounds from herbal medicine, its products and extracts. The objective of this study was to characterize a variety of particle sizes of Erythrina velutina Willd powder. The samples used in the study were named MUF01 (710 μm), MUF03 (180 μm) and MUF05 (75 μm). The techniques employed were scanning electron microscopy (SEM), thermal analysis such as thermogravimetry (TG) and differential thermal analysis (DTA) together with pyrolysis coupled to gas chromatography/mass spectrometry (Pyr-GC/MS). SEM enabled us to detect the existence of divergences from the expected results from the granulometry process. Thermal analytical techniques (TG and DTA) showed the thermal decomposition profile, corresponding to physical and chemical phenomena. The chromatographic data relative to the peak area of the compounds analyzed evidenced quantitative differences in the chemical compositions of the samples MUF01, MUF03, and MUF05 at 300, 450 and 600 °C. Neophytadiene 2,6,10-trimethyl, 14 and 3-eicosyne were identified by Pyr-GC/MS at 300, 450 and 600 °C, and it classified the samples according the peak area values, which were MUF05 > MUF03 > MUF01. SEM, DTA and TG confirmed this through particle size uniformity, heat flow, and mass loss, respectively. [ABSTRACT FROM AUTHOR]

Some environmental factors, including water availability, may influence seed germination. This study investigated the germination of E. velutina seeds submitted to different osmotic potentials and mobilization of reserves during water-stress. Scarified seeds were arranged in paper rolls and soaked in solutions of Polyethylene Glycol (PEG) prepared in osmotic potentials 0.0, -0.2, -0.4, -0.6, and -0.8 MPa and kept into a seed germinator, at 25 °C, and 12/12 h photoperiod (L/D), during 10 days. The percentage, mean time, mean speed, germination speed index; as well as the germination uniformity coefficient were assessed. During germination process the total soluble sugars, reducing sugars, soluble protein, and total amino acids were quantified in the cotyledon, hypocotyl and radicle of soaked seeds and cotyledons of quiescent seeds (control). There was influence of osmotic potential on E. velutina seed germination. The germination percentage remained at high levels until -0.6 MPa and above this osmotic potential there has been no germination. The mobilization of stored reserves of carbon and nitrogen in E. velutina seeds was also influenced by water-stress. There was sensitiveness between -0.2 and -0.6 MPa; however, the degradation and the mobilization of reserves was slower when the osmotic potential decreased [ABSTRACT FROM AUTHOR]

Context: Erythrina velutina (EV) Willd (Fabaceae-Faboideae) is a medicinal tree that is commonly used in Brazil for the treatment of several central nervous system disorders. Objective: The anticholinesterase activity of EV is described in this work. Methods: Concentration-response curves (0-1.6 mg/mL) for EV leaf aqueous extract (AE) and alkaloid-rich extracts (AKEs) were performed in vitro. Cholinesterase inhibition was examined in mouse brains, as the cholinesterase source, and in pure acetylcholinesterase (AChE) or butyrylcholinesterase (BuChE). Mice were treated with AE or AKE (100, 200, and 400 mg/kg, p.o.) and their brains were used for the measurement of cholinesterase activity (CA) ex vivo. Results: CA was inhibited by AE (IC50 = 0.57 [0.43-0.75] mg/mL) and AKE (IC50 = 0.52 [0.39-0.70] mg/mL) in brain homogenates in a concentration-dependent manner. The ex vivo experiments indicated that AE (400 mg/kg, p < 0.05, 32.2 ± 3.9% of inhibition) and AKE (all doses: p < 0.05- p < 0.001, 29.6 ± 3.2% as the maximum inhibition) significantly inhibited CA in the central nervous system after oral administration. AE and AKE inhibited AChE and BuChE activities in a concentration-dependent manner (AE: IC50AChE = 0.56 [0.38-0.81] mg/mL, IC50BuChE = 2.95 [1.51-5.76] mg/mL, AKE: IC50AChE = 0.87 [0.60-12.5] mg/mL, IC50BuChE = 2.67 [0.87-8.11] mg/mL). Discussion and conclusions: These data indicated that AE and AKE crossed the blood-brain barrier to inhibit CA in the brain. AE and AKE also exhibited a dual inhibitory action on acetyl- and BuChE. [ABSTRACT FROM AUTHOR]

Erythrina velutina (mulungu) is a native plant of the semi-arid region that can be propagated via tissue culture, which may contribute to the rapid multiplication of this species, reducing the possibility environmental impacts. The objective of this study was to establish a protocol for micropropagation of mulungu using aseptic explants seedlings grown in vitro. For the induction of shoots, , nodal segments and cotyledons were used as explants hypocontyl and were inoculated in a WPM culture medium supplemented with different concentrations of BAP and NAA. The rooting of shoots was achieved in a WPM medium supplemented with 0.0; 2.46; 4.92; 9.88μM IBA. The best answer to the multiplication was obtained in medium supplemented with 17.76μM BAP using nodal segment or cotyledonary node explants. The shoots rooted in all conditions tested, including the culture medium without auxin. [ABSTRACT FROM AUTHOR]

Abstract: Ethnopharmacological relevance: Erythrina velutina is traditionally used for sleepiness, convulsions and nervous system excitation in Brazil. Although central effects have been reported for Erythrina velutina, little is known about its mechanism of action. Aim of the study: To investigate the pharmacological evidences of mechanism of action of Erythrina velutina leaves aqueous extract (AE). Materials and methods: Terminal segments of the guinea-pig ileum (n =5–8) were mounted in an organ bath and isotonic contractions were recorded. Phytochemical screening was carried out on AE. Results: AE (0.025–2.50mg/ml) produced contractile response in the guinea-pig ileum, yielding typical concentration–response curves (EC50 =0.63mg/ml). Electrically evoked contractions were significantly increased in the presence of AE. AE-elicited contractions were significantly reduced by bicuculline, tetrodotoxin, atropine, verapamil or incubation in low calcium–high potassium solution. Atropine along with verapamil abolished AE contractile response. Alkaloids, catechins, steroids, flavonols, flavononols, flavonoids, phenols, saponins, tannins, triterpenoids, and xanthones were detected in AE. Conclusions: AE contains important constituents for pharmacological activities. AE-induced contractions seem to involve GABAA receptor activation, acetylcholine release, muscarinic receptor activation, augmentation of Ca2+ entry through L-type calcium channels, and calcium release from the intracellular stores. These findings provide further support for Erythrina velutina traditional uses. [Copyright &y& Elsevier]

The aim of this research was to study the influence of the sowing depth and position upon seedling emergency and seed vigor of the coral tree, some germination tests were settled in sand, under protected environment. The treatments were represented by the position and depth of the seed sowings relative to the substratum, as follows: seed with the hilum turned down, upward and to the side at depths 1, 2, 3, 4 and 5cm. Each treatment consisted of four replicates with 25 seeds, and were evaluated by the following tests: emergence, first- counting vigor, emergency speed, length and dry mass of the hypocotyl and roots. According to the results for coral tree, the sowing depth should be between one and two centimeters, whereas the best position was the hilum turned down. [ABSTRACT FROM AUTHOR]

Abstract: Introduction: In Brazil, Erythrina velutina (Fabaceae) is widely used as a tranquilizer and/or sedative, and its extract exerts an anxiolytic-like effect profile in animal models, although these results may be caused by its sedative or amnesic effects. Aims, materials and methods: Thus, this study evaluated the effect of acute and chronic (23–26 days) administrations of the hydroalcoholic extract of the stem bark of Erythrina velutina (orally) in mice submitted to the following tests: elevated plus-maze, forced swim, spontaneous locomotor activity, and habituation to active chamber. Chlordiazepoxide and imipramine were used as standard drugs. Results: In the elevated plus-maze test, chronic, but not acute, Erythrina velutina (100mg/kg) administration increased the percentage of open arm entries, an effect also seen in both acute and chronic treatments with chlordiazepoxide (7.5mg/kg). In the forced swim test, only imipramine (25mg/kg) decreased immobility time. Impairment of habituation was seen only with acute imipramine administration and with the lowest doses of Erythrina velutina extract tested in acute (10mg/kg) and chronic (50mg/kg) administrations. Conclusions: These results suggest that chronic administration of the hydroalcoholic extract of the stem bark of Erythrina velutina exerts an anxiolytic-like effect on mice, and it could serve as a new approach for the treatment anxiety, although it may have an amnesic effect at low doses. [Copyright &y& Elsevier]

In this work, we studied the effects of the alcohol extract (AE) from Erythrina velutina Willd (Fabaceae) leaves in animal models of anxiety (elevated plus maze; EPM), memory (inhibitory avoidance test), and epilepsy (pentylenetetrazol-induced convulsions and pentylenetetrazol-induced kindling seizure). In the EPM test, at the dose of 20 mg/kg, the AE significantly increased the percentage of entries into the open arms (p = 0.03). In the inhibitory avoidance test, greater test than training latencies were observed for the control group but not for the AE (10 mg/kg) (p = 0.112) and diazepam (p = 0.331) treated groups during the acquisition phase of the test. During the consolidation and retrieval phases, there were differences between training and test latencies for all three groups. In the pentylenetetrazol-induced convulsion test, the AE (100 mg/kg) increased the latency to death when compared with the control group (p < 0.05) and reduced the kindling behavior induced by low doses of pentylenetetrazol. Together, the effects described for the AE of E. velutina leaves on rodent central nervous system resemble the profile of effects of benzodiazepines and could be interpreted as an interaction of the extract with GABAergic circuitries. [ABSTRACT FROM AUTHOR]

Abstract: The anticonvulsant effects of hydroalcoholic extracts (HAEs) from the stem bark of Erythrina velutina and Erythrina mulungu on pentylenetetrazole (PTZ) and strychnine-induced seizure tests and the potentiation of pentobarbital-induced sleeping time in mice with the extracts were examined in this study. These medicinal plants belong to the Fabaceae family and are popularly used in Brazil for their effects on the central nervous system. The extracts of Erythrina velutina (intraperitoneally or orally) and Erythrina mulungu (intraperitoneally) were administered in mice at single doses (200 or 400mg/kg). While Erythrina velutina and Erythrina mulungu did not exhibit any protector effect in PTZ-induced seizures, at any dose, an increase in the latency of convulsion and in the death time was observed with both doses and routes of Erythrina velutina and at higher dose of Erythrina mulungu, in strychnine-induced seizure. No alteration was observed with Erythrina velutina and Erythrina mulungu on sleeping latency at both doses as compared to control (362.8±59.5). However, the sleeping time was increased in both plants as compared to control (943.8±129.6). In conclusion, we showed that the hydroalcoholic extracts of Erythrina velutina and Erythrina mulungu have anticonvulsant effects only in the strychnine-induced seizure model, suggesting their possible action in glycine system and a potentiation of pentobarbital sleeping time, suggesting depressant action in the central nervous system. [Copyright &y& Elsevier]

The aqueous extract (AE) of Erythrina velutina prolonged the sleep duration induced by sodium pentobarbital (control: 6.4 ± 1.2 min; extract 10 mg/kg, 47.1 ± 3.9 min; extract 100 mg/kg, 109.4 ± 7.2 min; F = 243, P < 0.001). In the open field, the extract at the doses of 10 and 50 mg/kg did not changed the number of crossings, rearings nor groomings. On the other hand, at the dose of 200 mg/kg it reduced the number of crossings (q = 6.25, P < 0.05) and groomings (q = 3.91, P < 0.05). When exposed during three consecutive days to the open field, the control animals showed habituation for crossings (F = 17.56, P < 0.001) and rearings (F = 14.01, P < 0.001). The same was not true for animals treated with 10 mg/kg of the extract (crossings: F = 3.59, P > 0.05; rearings: F = 3.62, P > 0.05). At the same dose, the extract blocked the acquisition of foot shock memory (P = 0.9219) when compared to the control values (P = 0.0078). Our data showed that the crude extract of Erythrina velutina at lower doses interferes with mnemonic process for different tasks, while at higher doses, the sedative and neuromuscular blocking actions are the main effects. [Copyright &y& Elsevier]

Two 4×4 Latin square design experiments were completed. In experiment 1, four mature Anglo-Nubian×Fiji goats were used to study effects of supplementation of a basal diet of maize stover with Erythrina variegata (E) Gliricidia sepium (G) and Leucaena leucocephala (L). Parameters measured were dry matter intake (DMI) and nutrient digestibility. Maize stover (MS) was treated with urea, used as a control diet, and had a crude protein (CP) content of 9.3%. Erythrina variegata was higher in CP than L and G. DMI of the urea-treated stover diet was lower (P<0.05) than the untreated MS supplemented with E, G or L. Among the legume supplements, DMI (g/kg W0.75 per day) was lower (P<0.05) in the MS/G diet compared to MS/E or MS/L diets. There were differences (P<0.05) between the urea-treated maize stover (UTMS) and MS with either E, G or L on the digestibility of dry matter (DM), CP, neutral detergent fibre (NDF), OM and energy (P<0.05), but no differences (P>0.05) among MS/L, MS/E and MS/G. In experiment 2, four mature goats were used to measure the response of goats when the UTMS; MS/legume diets were sprayed with molasses. The DMI (g/kg W0.75 per day) of the urea-treated MS sprayed with molasses was lower (P<0.05) than the MS/legume, but DMI among the MS/legume diets did not differ. The digestibility of DM, CP, NDF, OM and energy of urea-treated MS were lower (P<0.05) than values found for MS/legume diets. It is suggested that either E, G or L could be used as protein supplements to improve the nutritional quality of MS fed to mature goats. Addition of molasses to diets further improved DMI and apparent nutrient digestibility by the goats. This study shows the substantial effect of legume supplements on MS intake and digestibility by goats. Molasses, when available, should be sprayed on fresh leaves of Gliricidia sepium and other forage legumes, that are initially rejected, in order to improve their acceptance and DMI when fed in confinement or in cut-and-carry production systems. [Copyright &y& Elsevier]

Two new Erythrina alkaloid glycosides, 1 and 2 , and three new diarylpropanoid glycosides 12 – 14 together with nine known compounds were isolated from the MeOH extracts of the seeds of Erythrina velutina. The structures and absolute configurations of these new compounds were elucidated through comprehensive spectroscopic analyses as well as experimental and calculated ECD data. The inhibitory potency of these compounds against nitric oxide production in LPS-induced RAW 264.7 cells and the cytotoxicity of these compounds against the HeLa and HL-60 human cancer cell lines were also discussed. [Display omitted] [ABSTRACT FROM AUTHOR]

Abstract: A new Erythrinan alkaloid (1), erythodine N-oxide, was isolated from the seeds of Erythrina velutina together with seven known Erythrinan alkaloids (2–7, 9) and an indole alkaloid (8). The structure of new compound (1) was elucidated by spectroscopic methods. Six of the nine compounds showed enhanced activity when combined with tumor necrosis factor-related apoptosis-inducing ligand (TRAIL). Erysotrine (4) did not show cytotoxic activity by itself, but exhibited significant cytotoxicity when combined with TRAIL. [Copyright &y& Elsevier]

Abstract: An indole alkaloid (hypaphorine (1)) was isolated from Brazilian medicinal plant, Erythrina velutina (Leguminosae). This compound was investigated for sleep promoting effects in mice, and the results showed that it significantly increased non-rapid eye movement (NREM) sleep time during the first hour after its administration. The NREM sleep time was enhanced by 33% in the experimental mice when compared to that of the controls. This study therefore confirmed its sleep promoting property. [Copyright &y& Elsevier]

Mulungu é considerada uma espécie de uso medicinal também utilizada como madeireira, ornamental e industrial. A crescente demanda e o intenso extrativismo têm contribuído para a redução do número de plantas nas áreas de ocorrência natural desta espécie. Mulungu corre o risco de passar à categoria de espécie em perigo de extinção se continuar sendo explorada excessivamente e se sua sobrevivência não for assegurada. A pesquisa tem como objetivo proporcionar conhecimento científico para a conservação dessa espécie através de propagação sexuada utilizando diferentes substratos. O experimento foi conduzido de outubro a Novembro de 2013 no campus da Liberdade (UNILAB). As sementes de mulungu foram coletadas em árvores adultas no Município de Baturité-CE e submetidas a testes de emergência utilizando-se bandejas plásticas com os seguintes substratos: (T1) areia lavada, (T2) solo de jardim, (T3) solo de textura média, (T4) solo argiloso (T5) vermiculita. O delineamento experimental foi em blocos casualisados com 5 tratamentos e 5 repetições. No quinto dia após a semeadura foi feita a primeira coleta de dados, as plântulas consideradas emergidas foram as que emitiram o protófilo, os dados foram coletados diariamente por mais 8 dias quando o experimento foi encerrado por estabilização na germinação. Em seguida as plântulas foram retiradas dos substratos para medir-se com paquímetro digital o comprimento de raiz, diâmetro de caule, altura da parte aérea, e número de folhas, para análises de variância. Também foi feita contagem para calcular o percentual de emergência dos tratamentos. O software utilizado foi o ASSISTAT Versão 7.7 beta, onde se utilizou o teste de Tukey a 5% de significância para se calcular as médias. Os resultados mostraram que houve diferença significativa entre as médias ao nível de 1% de probabilidade para as características comprimento de raiz (CR), percentual de emergência (PE) e Índice de velocidade de emergência (IVE). A areia lavada (T1) foi o melhor substrato para comprimento de raiz (CR), percentual de emergência (PE) e índice de velocidade de emergência (IVE). Os substratos não interferiram no número de folhas (NF), comprimento de parte aérea (CPA) e diâmetro do caule (DC). Portanto concluise que o substrato de areia lavada é mais indicado para emergência de mulungu. [ABSTRACT FROM AUTHOR]