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1.
Front Pharmacol ; 13: 940988, 2022.
Article in English | MEDLINE | ID: mdl-35959438

ABSTRACT

Deverra tortuosa (Desf.) DC. and Deverra. triradiata Hochst. ex Bioss are perennial desert shrubs widely used traditionally for many purposes and they are characteristic for their essential oil. The objective of the present study was to investigate the in vivo wound healing activity of the essential oil (EO) of D. tortuosa and D. triradiata through their encapsulation into nanoemulsion. EO nanoemulsion was prepared using an aqueous phase titration method, and nanoemulsion zones were identified through the construction of phase diagrams. The EO was prepared by hydrodistillation (HD), microwave-assisted hydrodistillation (MAHD), and supercritical fluid extraction (SFE) and analyzed using GC/MS. D. tortuosa oil is rich in the non-oxygenated compound, representing 74.54, 73.02, and 41.19% in HD, MADH, and SFE, respectively, and sabinene represents the major monoterpene hydrocarbons. Moreover, D. triradiata is rich in oxygenated compounds being 69.77, 52.87, and 61.69% in HD, MADH, and SFE, respectively, with elemicin and myristicin as major phenylpropanoids. Topical application of the nanoemulsion of D. tortuosa and D. triradiata (1% or 2%) exhibited nearly 100% wound contraction and complete healing at day 16. Moreover, they exhibit significant antioxidant and anti-inflammatory effects and a significant increase in growth factors and hydroxyproline levels. Histopathological examination exhibited complete re-epithelialization accompanied by activated hair follicles and abundant collagen fibers, especially at a concentration of 2%. Therefore, the incorporation of the two Deverra species into nanoemulsion could professionally endorse different stages of wound healing.

2.
Front Chem ; 9: 760083, 2021.
Article in English | MEDLINE | ID: mdl-34722462

ABSTRACT

Endophytes are prolific producers of privileged secondary metabolites with diverse therapeutic potential, although their anticancer and antimicrobial potential still have a room for further investigation. Herein, seven known secondary metabolites namely, arugosin C (1), ergosterol (2), iso-emericellin (3), sterigmatocystin (4), dihydrosterigmatocystin (5), versicolorin B (6), and diorcinol (7) were isolated from the rice culture of Aspergillus sp. retrieved from Tecoma stans (L.) Juss. ex Kunth leaves. Their anticancer and antimicrobial activities were evaluated in MTT and agar well diffusion assays, respectively. The cytotoxicity results showed that metabolite 3 displayed the best viability inhibition on the MCF-7 breast cancer cells with IC50 = 225.21 µM, while 5 on the HepG2 hepatocellular carcinoma cells with IC50 = 161.81 µM. 5 demonstrated a 60% apoptotic mode of cell death which is virtually correlated to its high docking affinity to Hsp90 ATP binding cleft (binding score -8.4 Kcal/mol). On the other side, metabolites 4 and 5 displayed promising antimicrobial activity especially on Pseudomonas aeruginosa with MIC = 125 µg/ml. The observed effect may be likely related to their excellent in silico inhibition of the bacterial DNA-gyrase kinase domain (binding score -10.28 Kcal/mol). To the best of our knowledge, this study is the first to report the promising cytotoxic and antibacterial activities of metabolites 3, 4, and 5 which needs further investigation and renovation to therapeutic leads.

3.
Nat Prod Res ; 34(8): 1080-1090, 2020 Apr.
Article in English | MEDLINE | ID: mdl-30663363

ABSTRACT

Isoshamixanthone (1), a new stereoisomeric pyrano xanthone together with the previously known fungal metabolites, epiisoshamixanthone (2), sterigmatocystin (3), arugosin C (4), norlichexanthone (5), diorcinol (6), ergosterol and methyllinoleate, were obtained from the endophytic fungal strain Aspergillus sp. ASCLA isolated from leaf tissues of the medicinal plant Callistemon subulatus. The chemical structure of the new xanthone (1) was elucidated by extensive 1D, 2D NMR, and ESI HR mass measurements, and by comparison with literature data. The constitutions and absolute configurations of 1 and epiisoshamixanthone (2) were additionally confirmed by X-ray crystallography. Compounds 1,2 were evaluated for their potential anticancer activity using the human cervix carcinoma cell line (KB-3-1). The antimicrobial activities of the fungal extract and compounds 1,2 were studied using a panel of pathogenic microorganisms as well.


Subject(s)
Aspergillus/chemistry , Plants, Medicinal/microbiology , Xanthones/isolation & purification , Anti-Infective Agents/chemistry , Anti-Infective Agents/isolation & purification , Anti-Infective Agents/pharmacology , Antineoplastic Agents/chemistry , Antineoplastic Agents/isolation & purification , Antineoplastic Agents/pharmacology , Aspergillus/isolation & purification , Cell Line, Tumor , Crystallography, X-Ray , Ergosterol , Humans , Magnetic Resonance Spectroscopy , Molecular Conformation , Molecular Structure
4.
Acta Parasitol ; 62(2): 449-458, 2017 Jun 01.
Article in English | MEDLINE | ID: mdl-28426400

ABSTRACT

The Mascarene grass frog Ptychadena cf. mascareniensis is a species of frog with a vast area of distribution in Africa. A total of 300 frog specimens were collected from different localities at El-Giza province, Egypt; then dissected and examined for the presence of parasitic infection. Only eighty six (28.66%) specimens were found to be naturally infected with nematode parasite. Seasonally, the prevalence of infection was reached its maximum value of 74.66% during summer and minimum values of 26.66% (20/75), 13.33% (10/75) during spring and autumn, respectively; while no records were observed during winter season. The morphology of the recovered parasite was studied by using light and scanning electron microscopy. The adult worm characterized by anterior extremity with small mouth opening being surrounded by three lips provided with four sub-median cephalic papillae and one pair of lateral amphids. Body measurements showed that male worms were smaller than females measuring 1.22-2.43 (2.21 ± 0.1) mm in length and 0.21-0.34 (0.29 ± 0.01) mm in width. Females measured 1.9-3.7 (2.8 ± 0.1) mm in length and 0.24-0.42 (0.38 ± 0.01) mm in width. Comparing the present parasite with other species of the same genus described previously, several similarities were observed. However, peculiar new characteristics such as the arrangement of plectanes and somatic papillae, the presence of gubernaculum, the position of nerve ring, excretory pore, and vulval opening make it reasonable belongs to the family Cosmocercidae and identified as Cosmocerca sp. In addition, the present study was the first report for occurrence of cosmocercid species from the Mascarene grass frog in Egypt.


Subject(s)
Anura/parasitology , Nematoda/classification , Nematoda/ultrastructure , Animals , Female , Male , Microscopy, Electron, Scanning , Nematoda/isolation & purification , Sex Factors , Species Specificity
5.
Mem. Inst. Oswaldo Cruz ; 112(4): 247-254, Apr. 2017. graf
Article in English | LILACS | ID: biblio-841783

ABSTRACT

BACKGROUND Praziquantel has been cited as the only drug for treating schistosomiasis. However, concerns over drug resistance have encouraged the search for novel drug leads. The antimalarial drug primaquine possesses interesting anti-schistosmal properties. OBJECTIVES This study is the first to document the potential role of primaquine as a schistosomicide and the ultrastructural changes induced by primaquine on juvenile or adult male worms of Schistosoma mansoni. METHODS Ultrastructural alterations in the tegumental surface of 21-day-old juvenile and adult male worms of S. mansoni were demonstrated following primaquine treatment at different concentrations (2, 5, 10, 15, and 20 µg/mL) and incubation periods (1, 3, 6, 24, and 48 h) in vitro, using both scanning and transmission electron microscopy. FINDINGS At low concentrations (2, 5, and 10 µg/mL) both juvenile and adult male worms were alive after 24 h of incubation, whereas contraction, paralysis, and death of all worms were observed after 24 h of drug exposure at 20 µg/mL. The tegument of juvenile and adult male worms treated with primaquine exhibited erosion, peeling, and sloughing. Furthermore, extensive damage of both tegumental and subtegumental layers included embedded spines, and shrinkage of muscles with vacuoles. The in vitro results confirmed that primaquine has dose-dependent effects with 20 µg/mL as the most effective concentration in a short incubation period. MAIN CONCLUSIONS The schistosomicidal activity of primaquine indicates that this drug possesses moderate in vitro activity against juvenile and adult male worms, since it caused high mortality and tegumental alterations. This study confirmed that the antimalarial drug primaquine possesses anti-schistosomal activity. Further investigation is needed to elucidate its mechanism of action.


Subject(s)
Animals , Male , Praziquantel/pharmacology , Schistosoma mansoni/drug effects , Schistosoma mansoni/ultrastructure , Anthelmintics/pharmacology , Time Factors , Microscopy, Electron, Scanning , Cricetinae , Dose-Response Relationship, Drug
6.
Mem Inst Oswaldo Cruz ; 112(4): 247-254, 2017 Apr.
Article in English | MEDLINE | ID: mdl-28327785

ABSTRACT

BACKGROUND: Praziquantel has been cited as the only drug for treating schistosomiasis. However, concerns over drug resistance have encouraged the search for novel drug leads. The antimalarial drug primaquine possesses interesting anti-schistosmal properties. OBJECTIVES: This study is the first to document the potential role of primaquine as a schistosomicide and the ultrastructural changes induced by primaquine on juvenile or adult male worms of Schistosoma mansoni. METHODS: Ultrastructural alterations in the tegumental surface of 21-day-old juvenile and adult male worms of S. mansoni were demonstrated following primaquine treatment at different concentrations (2, 5, 10, 15, and 20 µg/mL) and incubation periods (1, 3, 6, 24, and 48 h) in vitro, using both scanning and transmission electron microscopy. FINDINGS: At low concentrations (2, 5, and 10 µg/mL) both juvenile and adult male worms were alive after 24 h of incubation, whereas contraction, paralysis, and death of all worms were observed after 24 h of drug exposure at 20 µg/mL. The tegument of juvenile and adult male worms treated with primaquine exhibited erosion, peeling, and sloughing. Furthermore, extensive damage of both tegumental and subtegumental layers included embedded spines, and shrinkage of muscles with vacuoles. The in vitro results confirmed that primaquine has dose-dependent effects with 20 µg/mL as the most effective concentration in a short incubation period. MAIN CONCLUSIONS: The schistosomicidal activity of primaquine indicates that this drug possesses moderate in vitro activity against juvenile and adult male worms, since it caused high mortality and tegumental alterations. This study confirmed that the antimalarial drug primaquine possesses anti-schistosomal activity. Further investigation is needed to elucidate its mechanism of action.


Subject(s)
Anthelmintics/pharmacology , Praziquantel/pharmacology , Primaquine/pharmacology , Schistosoma mansoni/drug effects , Schistosoma mansoni/ultrastructure , Animals , Cricetinae , Dose-Response Relationship, Drug , Male , Microscopy, Electron, Scanning , Microscopy, Electron, Transmission , Time Factors
7.
Parasitol Res ; 116(1): 133-141, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27757539

ABSTRACT

Myxozoans are one of the most economically important groups of protozoan parasites causing many serious diseases of their hosts. In the present study, a total of 60 live adult male specimens of the marsh frog Rana ridibunda have been randomly captured during the period of January-December 2015 in different areas at Kafr El-Sheikh Governorate, Egypt and were examined for infection by myxosporidian parasites. A total of 48 (80.0 %) out of 60 frog specimens were found to be infected with Myxobolus species. Parasitic infection was restricted to the testicular tissue of the examined frogs. Macroscopic cysts (plasmodia) which heavily infested different parts of the testes were recovered. Morphological and ultrastructural characteristics of these myxosporidian species were carried out using light and transmission electron microscopy. Plasmodia measured 0.16-0.53 (0.34 ± 0.01) mm in diameter. Mature spores appeared oval in frontal view, measuring 8.9-11.5 (9.6 ± 0.1) µm in length and 7.5-9.1 (8.4 ± 0.1) µm in width containing 5-6 turns of polar filaments. Morphometric characterization revealed that the very small size of the present Myxobolus species was the most distinctive feature that separates them from all previously described Myxobolus species. Ultrastructural analysis showed that the plasmodia are surrounded by a plasma membrane with numerous pinocytotic protrusions extending toward the host cell. The generative cells and the different developmental stages are arranged at the periphery of the plasmodia, while immature and mature spores are centrally located. Sporogenesis, capsulogenesis, valvogenesis, and spore maturation of the present parasite are also described. The present species is described as Myxobolus ridibundae and represents a new species.


Subject(s)
Myxobolus/physiology , Myxobolus/ultrastructure , Parasitic Diseases, Animal/parasitology , Rana ridibunda/parasitology , Testis/parasitology , Animals , Egypt , Male , Spores/physiology , Spores/ultrastructure , Wetlands
8.
J Parasit Dis ; 40(1): 145-51, 2016 Mar.
Article in English | MEDLINE | ID: mdl-27065615

ABSTRACT

Emergence of drug-resistant Fasciola strains has drawn the attention of many authors to alternative drugs. The purpose of this study is to explore the in vitro effect of the antimalarial mefloquine against adult Fasciola gigantica. Light and scanning electron microscopic observations could be used to determine the target of the drug following 6 and 12 h of incubation in medium containing mefloquine at three different concentrations 10, 20 and 30 µg/mL, as morphological changes could be observed. These changes occurred in definite sequences in response to mefloquine, and were consisted of swelling, vacuolization that was later disrupted, leading to desquamation of the tegument, resulting in exposure and disruption of basal lamina and the dislodging of spines. It is concluded that mefloquine presented itself as a drug that might become important in trematode chemotherapy, with the tegument being an important drug target.

9.
J Helminthol ; 90(6): 760-765, 2016 Nov.
Article in English | MEDLINE | ID: mdl-26824480

ABSTRACT

The present study tests the anti-inflammatory and anti-fibrotic effects of silymarin alone or combined with mefloquine on acute schistosomiasis by evaluating parasitological, histopathological, biochemical and immunological parameters. Male CDI Swiss mice were divided into seven groups, which included healthy controls, mice infected with Schistosoma mansoni or treated with silymarin (140 mg/kg body weight) or mefloquine (400 mg/kg body weight), or mice treated with a combination of both drugs and uninfected mice simply treated with mefloquine or silymarin alone. All mouse groups were sacrificed 8 weeks post-infection (pi) and/or post-treatment. Those infected mice treated with both silymarin and mefloquine showed a significant decrease (P <  0.001) in worm burden, immunoglobulins (IgG and IgM), liver function enzymes and granuloma diameter, with complete eradication of immature and mature eggs. In conclusion, treatment with silymarin combined with mefloquine in murine schistosomiasis was able to reduce granulomatous reactions and hepatic fibrosis. Hence, this combination is a new strategy to be studied as an efficient tool in the treatment of schistosomal liver fibrosis.


Subject(s)
Anthelmintics/administration & dosage , Drug Interactions , Fibrosis/pathology , Inflammation/pathology , Mefloquine/administration & dosage , Schistosomiasis mansoni/drug therapy , Silymarin/administration & dosage , Animals , Anthelmintics/pharmacology , Antibodies, Helminth/blood , Disease Models, Animal , Enzymes/blood , Granuloma/pathology , Liver Function Tests , Male , Mefloquine/pharmacology , Mice , Parasite Load , Schistosomiasis mansoni/parasitology , Schistosomiasis mansoni/pathology , Silymarin/pharmacology , Treatment Outcome
10.
Asian Pac J Trop Med ; 8(12): 999-1005, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26706670

ABSTRACT

OBJECTIVE: To assess the effect potency, and the immunomodulatory response of garlic oil extract in enhancing the host's immune system against the disorders caused by Schistosoma mansoni (S. mansoni) in mice at different stages of worm maturation. METHODS: A total of 70 male CD-1 Swiss albino mice were divided into 7 groups. Group I: healthy control. Group II: garlic oil group orally administrating 100 mg garlic oil extract/kg b.wt. 3 d a week for 6 weeks. Group III: infected with S. mansoni cercariae and left untreated for 42 d. Group IV: treated with garlic oil extract from day 1 to day 7 post infection (PI). Group V: treated with garlic oil extract from day 14 till day 21 PI. Group VI: administrating garlic oil extract from day 35 until day 42 PI. Group VII received oil extract from the first day of infection for 42 d. RESULTS: Garlic oil extract showed changes in the parasite tegument with a significant decrease in worm burden, hepatic and intestinal ova count with a decline in granuloma number and diameter. These alterations were accompanied with a reduction in serum TNF α, ICAM-1, IgG and IgM after 7 and 42 d post S. mansoni cercarial infection. CONCLUSIONS: Results obtained confirmed the effect of garlic oil extract on the larval and mature stage of the parasite and in enhancing the host's immune system against the disorders caused by S. mansoni in mice.

11.
Vet Parasitol ; 160(1-2): 76-82, 2009 Mar 09.
Article in English | MEDLINE | ID: mdl-19036519

ABSTRACT

Triclabendazole "Fasinex" is the drug of choice against fasciolosis because of its high efficacy against both mature and immature flukes, however parasite resistance against this drug is increasing. Hence, there is pressing need for new fasciolicidal drugs. In the present study, the in vitro effect of artemether on adult flukes was evaluated using scanning electron microscopy. After 24 h incubation with 10 microg/ml artemether, the tegument of the apical cone appeared to be slightly more swollen than normal. This swelling became so severe and the spines appeared sunken, with their tips protruding from a swollen and blebbed base, on increasing the concentration to 20 microg/ml. With the higher concentration of 30 microg/ml, extensive and severe tegumental swelling occurred in the apical cone region of the flukes. There were many blebs around ventral sucker, a number of which appeared to have burst causing lesion. The tegumental changes occurred following incubation in artemether were comparable with those observed with triclabendazole in its active sulphoxide metabolite form (TCBZ-SX).


Subject(s)
Anthelmintics/pharmacology , Artemisinins/pharmacology , Benzimidazoles/pharmacology , Fasciola/drug effects , Animals , Artemether , Fasciola/ultrastructure , Triclabendazole
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