This study investigates updated information in different search engines on the distribution, phytochemistry, pharmacology, and toxicology of Brugmansia suaveolens (Solanaceae) using the extracts or chemical compounds at present. This plant has been used in traditional medicine in different cultures as a hallucinatory, analgesic, aphrodisiac, nematicide, sleep inducer, and muscle relaxant, as well as a treatment for rheumatism, asthma, and inflammation. The flowers, fruits, stems, and roots of the plant are used, and different chemical compounds have been identified, such as alkaloids, volatile compounds (mainly terpenes), coumarins, flavonoids, steroids, and hydrocarbons. The concentration of the different compounds varies according to the biotic and abiotic factors to which the plant is exposed. The toxic effect of the plant is mainly attributed to atropine and scopolamine, their averages in the flowers are 0.79 ± 0.03 and 0.72 ± 0.05 mg/g of dry plant, respectively. Pharmacological studies have shown that an aqueous extract exhibits the antinociceptive effect, at doses of 100 and 300 mg/kg i.p. in mice. On the other hand, the ethanolic extract at 1000 mg/L, showed a nematocidal activity in vitro of 64% against Meloidogyne incognita in 72 h. Likewise, it showed a 100% larvicidal activity at 12.5 mg/L against Ancylostoma spp. In another study, the lethal activity of shrimp in brine from an ethanolic extract showed an LC₅₀ of 106 µg/mL at double serial concentrations of 1000–0 (µg/mL). Although there are pharmacological and phytochemical studies in the plant, they are still scarce, which has potential for the examination of the biological activity of the more than one hundred compounds that have been reported, many of which have not been evaluated.

En esta investigación evaluamos la actividad insecticida de una fracción acuosa de tallos de Serjania schiedeana Schltdl. (Sapindaceae) (FASs), a concentraciones de 250, 500, 1,000, 1,500, y 2,000 ppm, en laboratorio e invernadero en plantas de maíz sobre larvas neonatas de Spodoptera frugiperda Smith (Lepidoptera: Noctuidae). Los resultados de los bioensayos de laboratorio mostraron que a los 14 días el FASs a 250 y 1,500 ppm inhibió 50 y 20% el peso larval del insecto. La FASs en todas sus concentraciones ocasionó una mortalidad larval superior a 50% y una mortalidad total de larvas + pupas del 100%, excepto a 500 ppm. En el invernadero, a partir del día siete las plantas de maíz asperjadas con FASs a 250 y 2,000 ppm disminuyeron el daño de las larvas en más del 18%. Un perfil fitoquímico de la FASs, resultó positivo para alcaloides, flavonoides y taninos, estos compuestos podrían tener relación con el efecto insecticida contra S. frugiperda. Los resultados demuestran que la FASs puede ser considerada para el desarrollo de nuevos insecticidas botánicos y posiblemente ser considerados en el control integrado de plagas.

Mental and neurological disorders are conditions that affect thoughts, emotions, behavior, and relationships. Malpighia mexicana A. Juss. is a plant used in Mexican traditional medicine for the treatment of such disorders. This work aimed to investigate the antidepressant, anxiolytic, sedative, hypnotic, and anticonvulsant effects of the acetonic extract (MmAE) of M. mexicana and its fractions (F3, F4-10, F14) using the forced swimming test (FST), elevated plus maze (EPM), open field test (OFT), pentobarbital-induced sleep test (PBTt), and pentylenetetrazol-induced seizure test (PTZt). MmAE, F3, F4-10, F14, and vehicle were administrated orally 24, 18, and 1 h prior to the evaluations. Imipramine (15 mg/kg, p.o.) was administrated 1 h prior to the evaluations as a positive control for the FST, while diazepam (1 mg/kg, p.o.) was administrated 1 h prior to the evaluations as a positive control for the EPM, OFT, PBTt, and PTZt. MmAE had an anxiolytic effect; MmAE and F3, F4-10, and F14 showed an antidepressant effect, sedative effect, hypnotic effect, and anticonvulsant effect. Using HPLC, we identified the compounds quercetin 3-O-rutinoside (1), kaempferol 3-O-glucoside (2), luteolin 7-O-glucoside (3), quercetin (4), and kaempferol (5) in MmAE and compounds (1), (2), and (3) in F14. Using GC-MS, we identified α-tocopherol, phytol, and β-amyrin in F3; β-tocopherol, phytol, β-sitosterol, and β-amyrin in F4-10; and α- tocopherol, phytol, β-sitosterol, and β-amyrin in F4-10. The neuropharmacological effects found in this work may be due to the presence of vitamins, phytosterols, terpenes, and flavonoids. This research requires further study to clarify the mechanisms of action of the identified compounds.

Pharmacological Interaction between Galphimine-A, a Natural Anxiolytic Compound and Gabaergic Drugs

The frequent and indiscriminate use of all classes of synthetic anthelmintics to deworm small ruminants has decreased their effectiveness in a worldwide problem of anthelmintic resistance. Using active plant metabolites with anthelmintic properties has become a suggested alternative to control parasitic helminths. The present study investigated the ovicidal and larvicidal activity of a fraction (CnF4) containing protocatechuic acid (3,4-dihydroxybenzoic acid) from Chamaecrista nictitans (Fabaceae) and a commercial standard of protocatechuic acid against strains of the parasitic nematode Haemonchus contortus susceptible (HcIVM-S) and resistant (HcIVM-R) to ivermectin, using egg hatch inhibition (EHI) and L3 larval mortality assays. The CnF4 fraction showed an EHI greater than 90% at 0.8 mg/mL against HcIVM-S and an EHI = 88.39% at 1.6 mg/mL against HcIVM-R. The commercial standard of protocatechuic acid displayed an EHI of 97.49% at 0.25 mg/mL against HcIVM-S and an EHI greater than 98% at 0.5 mg/mL. In the larval mortality assays, protocatechuic acid caused 72.4% larval mortality of HcIVM-S at 8 mg/mL and 53.2% mortality of HcIVM-R at 16 mg/mL. These results indicate that protocatechuic acid was more effective in inhibiting egg hatching and causing larval mortality against HcIVM-S compared to HcIVM-R.

In this study, we tested the insectistatic and insecticidal effects of the ethanolic extract of stems and bark of Ficus petiolaris Kunth (Moraceae) in laboratory bioassays with an artificial diet against newly hatched larvae of the fall armyworm, Spodoptera frugiperda Smith (Lepidoptera: Noctuidae). The extract was evaluated at five different concentrations (500, 1000, 1500, 2000, and 2500 ppm). The 2500 ppm extract had the strongest inhibitory effects on larval (89%) and pupal (20%) weight as well as the highest mortality (80%). The positive control, methyl parathion (Methyl Parathion^®) at 1%, eliminated 100% of the fall armyworm, and the negative control (artificial diet) had a mortality of only 5%. Chemical fractionation of F. petiolaris stem and bark extract produced five fractions of FpR1-5, each of which was evaluated at 250, 500, 750, 1000, and 1250 ppm. FpR4 presented the strongest inhibitory effect, reducing the weight of the larva and pupa by 35% and 18%, while FpR2 had the strongest insecticidal effect, with 90% mortality at 1250 ppm. The pure 8-Methoxypsoralen compound extracted from this fraction was even more effective, with 100% S. frugiperda mortality at 100 ppm. The 50% lethal concentration (LC₅₀) of 8-Methoxypsoralen was 67.68 ppm. Our results indicate that the F. petiolaris extract showed toxic activity against the fall armyworm, and its compound 8-Methoxypsoralen showed strong insecticidal activity at low concentrations.