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1.
Pak J Pharm Sci ; 35(5): 1287-1294, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-36451555

RESUMO

Aristolochia bracteolatais utilized in confronting multiple and complicated disease conditions such as cancer, lung inflammation, dysentery, syphilis, gonorrhea, arthritis, skindiseases, snake bite and oxidative stress relating to humans due to their acceptability, affordability and proximity. This investigation seeks to determine the antioxidant and anti-diabetic effects of methanol extract of A. bracteolate root bark in vitro. The phytochemical screening, antioxidant, and enzymes inhibitory (alpha-amylase and alpha-glucosidase) properties of root bark extract were evaluated by standard procedures. The methanol extract indicated the presence of diverse phytochemicals (tannins, saponins, flavonoids, alkaloids, phenols, glycosides and terpenoids) and contained a remarkable amount of saponins (8.20±0.03%), phenols (6.82±0.01%), alkaloids (4.71±0.03%) and flavonoids (3.50±0.12%). The extract showed not only strong antioxidant properties against DPPH, FRAP and TBARS radicals with IC50 value of 57.87, 54.64 and 47.54 mg/ml, respectively but also anti-diabetic activity by inhibiting alpha-amylase (IC50=53.70 mg/ml) and alpha-glucosidase (IC50=49.18 mg/ml). GC-MS chromatogram identified a diverse array of active metabolites in the methanol extract of A. bracteolate root bark. This study suggested that the methanol extract of A. bracteolate root bark possessed anti-oxidative and anti-diabetic activities.


Assuntos
Aristolochia , Saponinas , Humanos , Metanol , Antioxidantes/farmacologia , Cromatografia Gasosa-Espectrometria de Massas , alfa-Glucosidases , Casca de Planta , Fenóis , Flavonoides/farmacologia , alfa-Amilases , Amilases , Extratos Vegetais/farmacologia
2.
Comput Biol Med ; 148: 105865, 2022 09.
Artigo em Inglês | MEDLINE | ID: mdl-35843194

RESUMO

Autoimmune diseases develop when the immune system targets healthy cells and tissues of an individual. In developing countries, S. typhi (a gram-negative pathogenic bacteria) remains a major public health issue. This study aimed to employ bioinformatics analyses to determine the 3D structural-based molecular mimicry and sequence of S. typhi and human host proteins. In addition, to classify possible antigenic microbial peptides homologous to human peptides and comprehend the molecular basis of S. typhi-related autoimmune disorders. Protein sequences were obtained from the NCBI database, and redundancy was removed using the CD-HIT tool. The BLASTp comparative sequence analysis was followed for molecular mimicry identification of human and S. typhi protein sequences. The PathDIP database was utilized to simulate essential physical relationships between proteins and curated pathways for metabolic processes. Subsequently, the IEDB database was used to find cross-reactive MHC class-II binding epitopes that could trigger an autoimmune reaction. SPARKS-X computational biology resource was also used to determine the structural homology between human and S. typhi peptides. The BLASTp study showed that S. typhi and the human host have several proteins holding considerable sequence similarities based on a set threshold of e ≤ 10-6 and bit score ≥100. The PathDIP putatively identified that these proteins enriched in a total of 68 metabolic pathways by a significant P-value (P < 0.005). The PSORTb analysis predicted that 26 out of these proteins are cytosolic, 1 predicted to be periplasmic protein, and 1 predicted to be localized in the cytoplasmic membrane. IEDB data analysis predicted many S.typhi and human homologs epitopes as a good binder of human HLA, i.e. DRB1*01:01, DPA1*03:01/DPB1*04:02, and DQA1*01:02/DQB1*06:02 with IC50 < 50 nM. Finally, the docking data demonstrated that homolog lead epitopes promisingly interact with HLA and immune TLR4 receptors by exhibiting the best docking scores and molecular interactions. The analyses ultimately identified several potential candidate proteins and peptides that could cause S.typhi infection-mediated autoimmune diseases in humans.


Assuntos
Doenças Autoimunes , Salmonella typhi , Autoimunidade , Epitopos , Humanos , Mimetismo Molecular
3.
Artigo em Inglês | IMSEAR | ID: sea-150901

RESUMO

The medicinal value of plants lies in bioactive phytochemical constituents that produce definite physiological actions on the human body. Some of the most important bioactive phytochemical constituents are Tannin, Alkaloids, Saponins, Flavonoids, Steroids, Anthraquinones, Coumarins and Sterols and Terpenes. Infectious diseases are the leading cause of death worldwide, accounting for nearly one half of all deaths in tropical countries which are also becoming a significant problem in developed countries. Therefore the present study was aimed to analyzed the phytochemicals and antimicrobial activities of Mentha spicata. The phytochemical constituents were determined by using known literature method while the antimicrobial activity was analyzed by classical literature methods. In case of phytochemicals, Tannin, Alkaloids, Glycosides, Flavonoids, Steroids, Coumarines, Sterols and Terpenes were found while saponins and anthraquinones were not determined in all the samples. Antibacterial activity was noted high in all the samples of crude extract followed by ethyl acetate and lowest activity was found was found in aqueous extract of Mentha spicata. The Same results were analyzed for antifungal activity.

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