Phytoconstituents of Terminalia catappa Linn Fruits Extract Exhibit Promising Antidiabetic Activities Against α-Amylase and α-Glucosidase In Vitro and In Silico DOI Creative Commons
Fitri Amelia, Hesty Parbuntari,

Iryani

и другие.

Informatics in Medicine Unlocked, Год журнала: 2024, Номер 47, С. 101509 - 101509

Опубликована: Янв. 1, 2024

Terminalia Catappa fruits are recognized for their use in diabetes treatment, yet the mechanism by which they inhibit diabetes-related enzymes remain largely undefined. This study aimed to elucidate therapeutic potential and interactions of T. catappa fruit extract through vitro silico approaches. The compounds from were extracted using microwave-assisted extraction techniques, followed qualitative phytochemical screening quantitative analysis via GC-MS. physicochemical properties evaluated according Lipinski rule ADMET criteria. Antidiabetic analyses, both silico, performed on secondary metabolites found fruit, targeting α-amylase α-glucosidase enzymes. methanol ethyl acetate extracts contained alkaloids, flavonoids, saponins, steroids, terpenoids. These inhibited a dose-dependent manner, with showing significantly higher inhibitory activity than pure acarbose (by two- five-fold, respectively) extract. Furthermore, antioxidant methanolic was seven times greater that Molecular docking studies supported these findings, revealing ΔG values gibberellic acid, rescinnamine, digoxin comparable those acarbose. Notably, has against acarbose, while nerolidol showed similar Gibberellic unique extract, demonstrated high values, suggesting its significant role extract's enhanced glucosidase amylase activities. identifies specific (digitoxin, nerolidol) proposes multi-target drugs treatment. Understanding constituents effects diabetes-involved could benefit individuals type 2 diabetes, particularly at risk complications.

Язык: Английский

Design, synthesis and bioevaluation of new vanillin hybrid as multitarget inhibitor of α-glucosidase, α-amylase, PTP-1B and DPP4 for the treatment of type-II diabetes DOI Creative Commons
Mohammed Ayed Huneif, Dhafer Alshehri, Khaled S. Alshaibari

и другие.

Biomedicine & Pharmacotherapy, Год журнала: 2022, Номер 150, С. 113038 - 113038

Опубликована: Апрель 28, 2022

Diabetes mellitus (DM) is a real challenge to the recent era and one of major diseases for initiating life-threatening disorders. In current research, compound was designed by combining vanillin, thiazolidinedione morpholine. The goal our work demonstrate ability design (9) modulate more than target responsible hyperglycemia at same time. synthesized able show good moderate inhibition potential against α-glucosidase, α-amylase protein tyrosine phosphatase 1B. However, it exhibited excellent in-vitro Dipeptidyl peptidase-4 (DPP-4) with IC50 value 0.09 µM. Antioxidant activity using DPPH assay also showed its antioxidant potential. in-vivo experiments, 9 proved be safe in experimental mice. profile observed 21 days which that effective Binding orientations Interactions key amino acid residues selected targets were studied docking studies. Overall, we successful synthesizing multitarget preclinical therapeutic three pharmacophoric moieties into single chemical entity can

Язык: Английский

Процитировано

50

Underlying Anticancer Mechanisms and Synergistic Combinations of Phytochemicals with Cancer Chemotherapeutics: Potential Benefits and Risks DOI Creative Commons
Muhammad Ayaz, Asif Nawaz, Sajjad Ahmad

и другие.

Journal of Food Quality, Год журнала: 2022, Номер 2022, С. 1 - 15

Опубликована: Июнь 15, 2022

Cancer therapies are associated with various challenges including the emergence of multidrug resistant tumors, toxicological issues, severe side effects, and economic burden. To counteract these natural products as substitutes adjuvant have received considerable attention owing to their safety, efficacy, aspects. Various preclinical clinical studies revealed that combinations chemotherapeutics mediate anticancer effects via modulation signaling pathways implicated in promoting apoptosis, inhibiting excessive cellular proliferation, mobilizing immune system. Several lead phytochemicals curcumin, resveratrol, quercetin, cannabinoids synergistically act cancer reducing cell proliferation inducing apoptosis cycle arrest. However, on subject matter limited need further extensive studies. It has been observed patients undergoing chemotherapy use alternative ameliorate symptoms chemotherapeutic agents. Nevertheless, some inform physicians regarding herbal medicine during while others do not, even most not know composition they consume chemotherapy. Herbal interactions both beneficial harmful aspects, but aspect overweighs ones terms controlling Nonetheless, a large number medicines demonstrated synergistic effect alleviate The concomitant majority be multiple malignant tumors like blood, lungs, kidneys, liver, skin, gastrointestinal tract. which possess positive interaction improve quality life should sorted out integrated There control system for appraisal medicine, there also an appropriate patient-doctor communication counsel deleterious combination

Язык: Английский

Процитировано

31

Anti-diabetic Activity of Brucine in Streptozotocin-Induced Rats:In Silico,In Vitro, andIn VivoStudies DOI Creative Commons
Naimat Ullah Khan, Neelum Gul Qazi,

Arif‐ullah Khan

и другие.

ACS Omega, Год журнала: 2022, Номер 7(50), С. 46358 - 46370

Опубликована: Дек. 8, 2022

Diabetes mellitus (DM) is a complex and multiple group of disorders, understanding the molecular mechanisms key role in identifying various markers involved diagnosis disease. Brucine derived from seeds Strychnos nux-vomica L. (Loganiaceae), which has been used traditional medicine to cure variety ailments, such as chronic rheumatism, nervous system diseases, dyspepsia, gonorrhea, anemia, bronchitis, analgesic, anti-inflammatory, anti-oxidant, anti-snake venom, anti-diabetic properties. The potential brucine was studied utilizing vitro, silico, vivo, methods, including streptozotocin-induced diabetic rat models, α-glucosidase α-amylase inhibitory assays, via Auto-DocVina software. exhibits binding affinities -5.0 -10.1 Kcal/mol against chosen protein targets, according an silico investigation. In vitro studies revealed that inhibited enzymes α-glucosidase, (20 mg/kg) reduced blood glucose levels, oral tolerance overload, body weight, glycosylated hemoglobin total cholesterol, triglycerides, low-density lipoprotein, alanine transaminase, aspartate aminotransferase, bilirubin, alkaline phosphatase elevated high-density lipoprotein levels vivo studies. energy certain targets ranges Kcal/mol. It anti-diabetic, anti-hyperlipidemic, hepatoprotective, anti-inflammatory properties, are mediated inhibition α-amylase.

Язык: Английский

Процитировано

23

Antioxidant and Hypoglycemic Potential of Essential Oils in Diabetes Mellitus and Its Complications DOI Open Access

Simona Bungău,

Cosmin Mihai Vesa,

Cristian Bustea

и другие.

International Journal of Molecular Sciences, Год журнала: 2023, Номер 24(22), С. 16501 - 16501

Опубликована: Ноя. 19, 2023

Since the earliest times, essential oils (EOs) have been utilized for medicinal and traditional purposes. However, in recent decades, an increasing interest has developed due to need rediscover herbal remedies adjuvant therapies management of various diseases, particularly chronic ones. The present narrative review examines potential EOs exert hypoglycemic antioxidant effects diabetes mellitus, analyzing main publications having evaluated plant species with potentially beneficial through their phytocompounds mellitus its complications. Numerous shown promising characteristics that can be used management. these are attributed capacity stimulate glucose uptake, suppress production, increase insulin sensitivity. Moreover, alleviate oxidative stress by manifesting via a variety mechanisms, including scavenging free radicals, regulation enzymes, decreasing lipid peroxidation, diverse chemical composition. These findings demonstrate possible benefits as therapeutic agents use treatment shows good development natural effective strategies enhance health outcomes people this condition, but additional experimental endorsements required.

Язык: Английский

Процитировано

14

Novel acyl hydrazide derivatives of polyhydroquinoline as potent anti-diabetic and anti-glycating agents: Synthesis, in vitro α-amylase, α-glucosidase inhibition and anti-glycating activity with molecular docking insights DOI
Sajjad ur Rahman, Aftab Alam, Zahida Parveen

и другие.

Bioorganic Chemistry, Год журнала: 2024, Номер 150, С. 107501 - 107501

Опубликована: Май 31, 2024

Язык: Английский

Процитировано

5

Prospective role of lupeol from Pterocarpus santalinus leaf against diabetes: An in vitro, in silico, and in vivo investigation DOI
Suvro Biswas, Mohasana Akter Mita, Shirmin Islam

и другие.

Computers in Biology and Medicine, Год журнала: 2025, Номер 186, С. 109680 - 109680

Опубликована: Янв. 21, 2025

Язык: Английский

Процитировано

0

Phytochemical Investigation and <i>In Vitro</i> Antidiabetic Potential of Leaf Extracts of Himalayan Herb: <i>Allium stracheyi</i> Baker DOI Open Access

Lata Bisht,

Neeraj Kumar,

Veerma Ram

и другие.

Journal of Natural Remedies, Год журнала: 2025, Номер unknown, С. 141 - 150

Опубликована: Янв. 31, 2025

Background: Various species of the genus Allium have been reported to exhibit antidiabetic potential. Among various species, stracheyi Baker is one most popular and important ethnobotanical traditional perennial Himalayan seasoning herbs belonging family Alliaceae. Since no scientific studies carried out assess potential in reducing blood sugar levels. Therefore, present research work aimed screen different leaf extracts for presence bioactive phytochemicals evaluate vitro each extract. Aim: To ascertain phytochemical composition by using preliminary qualitative quantitative screening methods assessment enzymatic assays. Methods: The successive extraction was a sequence solvents with increasing polarity including petroleum ether, methanol, hydroalcoholic water soxhlation apparatus. concentrated were subjected analysis or absence active their quantity extract followed determination application standard Results: Phytochemical on confirmed phytochemicals. Results showed that methanolic possesses highest amount phenolic flavonoids which may contribute plant. All demonstrated marked (α-amylase α-glucosidase) Additionally, only tested significant Conclusion: Research findings concluded methanol exhibited because existence compounds as well majority. Further additional plant are strongly suggested isolate purify major phenolics from confirm its vivo studies. Major Findings: This study’s main finding that, all extracts, effective at inhibiting activity alpha-glucosidase enzyme (IC50=32.92 μg/ml 100 μg/ml) alpha-amylase (IC50=50.51 μg/m μg/ml), suggests it be used treat diabetes. high concentration polyphenolic chemicals, tannins, steroids, alkaloids, saponins, what causes this activity.

Язык: Английский

Процитировано

0

Chemical composition and biological activities of essential oil from Illigera rhodantha Hance. (Hernandiaceae) from Vietnam DOI
Tuan Quoc Doan, Nguyễn Thị Thu Hoài,

Trang Huyen Xuan Hoang

и другие.

Journal of Essential Oil Bearing Plants, Год журнала: 2025, Номер unknown, С. 1 - 9

Опубликована: Апрель 7, 2025

Язык: Английский

Процитировано

0

Exploring the bio-insecticidal activity of Eucalyptus globulus essential oil/β-cyclodextrin inclusion complexes: In vitro and in silico assessment against Ephestia kuehniella larvae DOI

Fakhreddine Ben Amara,

Sarra Akermi, Fatma Driss

и другие.

Pesticide Biochemistry and Physiology, Год журнала: 2024, Номер 202, С. 105917 - 105917

Опубликована: Апрель 20, 2024

Язык: Английский

Процитировано

3

Phytochemistry, anti-diabetic and antioxidant potentials of Allium consanguineum Kunth DOI Creative Commons
Mater H. Mahnashi, Yahya S. Alqahtani,

Ali O. Alqarni

и другие.

BMC Complementary Medicine and Therapies, Год журнала: 2022, Номер 22(1)

Опубликована: Июнь 13, 2022

The study was planned to investigate the phytochemicals, antidiabetic and antioxidant studies of A. consanguineum.The preliminary were performed on crude extract different solvent fractions. Based potency, chloroform fraction semi-purified phyto-fractions CHF-1 - 5. Furthermore, CHF-3 subjected isolation pure compounds using column chromatography. α-glucosidase, α-amylase assays (DPPH, ABTS, H2O2) all samples. in-vivo experiments 1 2 also oral glucose tolerance test. Docking α-glucosidase targets.Among fractions, exhibited excellent activities profile giving IC50 values 824, 55, 117, 58 85 μg/ml against α-amylase, DPPH, ABTS H2O2 targets respectively. Among five (CHF-1-5), leading in 85.54, 61.19 26.58 DPPH overall potency physical amount CHF-3, it purification get 2. two found potent in-vitro activities. observed for compound 7.93, 28.01 6.19 Similarly, 14.63, 24.82 7.654 Compounds decreasing blood levels experimental animals. showed interactions with respective enzymes molecular docking.We can conclude that Consanguineum is a rich source natural agents. Bioguided potential inhibitions tested targets. Further, both able decrease

Язык: Английский

Процитировано

15