Pub Date : 2024-10-18DOI: 10.1007/s13596-024-00795-6
Udaykumar G. Vegad, Jigna Vadalia, Nira Kalwani, Bhavinkumar Gayakvad, Riya A. Desai, Vaibhav Bhatt, Sanjay P. Chauhan, Devang J. Pandya
Gojihva or Gaozaban, an Ayurvedic and Unani medicinal plant, is a commercially important drug with a controversial botanical origin. Onosma bracteata, officially considered Gojihva in India, has very few scientific validations of traditional claims, and few attempts have been made to standardise the plant. The successive extracts were screened for in vitro DPPH assay and hepatoprotective activities (HepG2 cells) to evaluate the traditional claim of vishaghna - antitoxic. The methanol extract has the highest antioxidant capacity of 88.48 ± 0.00% at a concentration of 62.5 µg/mL. The methanol extract at a concentration of 125 µg/mL and above exhibited significant protection against paracetamol and carbon tetrachloride-induced toxicity compared to the control group and other extracts. The caffeic acid and β-sitosterol were isolated from methanol extract, with the latter being reported for the first time. A high-performance thin layer chromatography method was developed for estimating two compounds. The content of caffeic acid and β-sitosterol was found to be 19.06 mg/100 g and 40.42 mg/100 g of the plant material, respectively. Our studies have validated the hepatoprotective property and established quality parameters that are useful for standardisation of O. bracteata and distinguishing it from the other species of Gojihva.
{"title":"Bioactivity-guided isolation and estimation of hepatoprotective marker compounds from Onosma bracteata; a species of the controversial drug ‘Gojihva’","authors":"Udaykumar G. Vegad, Jigna Vadalia, Nira Kalwani, Bhavinkumar Gayakvad, Riya A. Desai, Vaibhav Bhatt, Sanjay P. Chauhan, Devang J. Pandya","doi":"10.1007/s13596-024-00795-6","DOIUrl":"10.1007/s13596-024-00795-6","url":null,"abstract":"<div><p><i>Gojihva</i> or <i>Gaozaban</i>, an Ayurvedic and Unani medicinal plant, is a commercially important drug with a controversial botanical origin. <i>Onosma bracteata</i>, officially considered <i>Gojihva</i> in India, has very few scientific validations of traditional claims, and few attempts have been made to standardise the plant. The successive extracts were screened for in vitro DPPH assay and hepatoprotective activities (HepG2 cells) to evaluate the traditional claim of <i>vishaghna</i> - antitoxic. The methanol extract has the highest antioxidant capacity of 88.48 ± 0.00% at a concentration of 62.5 µg/mL. The methanol extract at a concentration of 125 µg/mL and above exhibited significant protection against paracetamol and carbon tetrachloride-induced toxicity compared to the control group and other extracts. The caffeic acid and β-sitosterol were isolated from methanol extract, with the latter being reported for the first time. A high-performance thin layer chromatography method was developed for estimating two compounds. The content of caffeic acid and β-sitosterol was found to be 19.06 mg/100 g and 40.42 mg/100 g of the plant material, respectively. Our studies have validated the hepatoprotective property and established quality parameters that are useful for standardisation of <i>O. bracteata</i> and distinguishing it from the other species of <i>Gojihva</i>.</p><h3>Graphical Abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":7613,"journal":{"name":"Advances in Traditional Medicine","volume":"25 2","pages":"523 - 536"},"PeriodicalIF":1.8,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144091211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rice has been reported to possess a variety of biological activities and non-colored rice demonstrates the activities less potent than colored rice. Pathum Thani fragrant rice is new strain non-colored Thai rice that become highly consumed rice. Due to less potent activity, an increase in activity of the non-colored rice is needed to perform. Cereals are rich in active compounds and exhibit a number of activities. To verify whether combination with cereals could enhance the activities of the non colored rice, therefore this study was carried out to determine chemical components, antioxidant and antidiabetic activities of ethanol extracts from Pathum Thani fragrant rice both individual and combination with cereals, compared to those from Black rice. GC-MS analysis revealed the presence of 32, 48, 63, and 66 chemicals in the ethanol extracts from Pathum Thani fragrant rice extract (PTRE), Pathum Thani fragrant rice extract combined with cereals (PTRCE), Black rice extract (BRE), and Black rice extract combined with cereals (BRCE), respectively. The docking study showed that 9-Octadecadienoic acid (Z, Z)-, one of the predominant chemicals in the extracts interacted in the active site pocket of α-glucosidase and α-amylase. PTRE exhibited antioxidant activity by DPPH scavenging activity and antidiabetic activity by inhibiting α-glucosidase activity, increasing body weight and serum insulin levels and reducing blood glucose levels in STZ diabetic rats. Interestingly, PTRCE exerted higher affective activities higher compared to PTRE. The results indicate that Pathum Thani fragrant rice can be enhanced the activities and developed as a therapeutic agent for management of free radical-related diseases and diabetes mellitus, by combination with cereals.
{"title":"Chemical components, antioxidant activity and antidiabetic activity (in vitro, in silico and in vivo, streptozotocin-induced diabetic rats) of extracts from Pathum Thani fragrant rice","authors":"Sompong Sansenya, Nopparat Buddhakala, Apirak Payaka, Orathai Sarakul, Moragote Buddhakala, Manatchanok Kongdin, Sasiprapha Asawawibul","doi":"10.1007/s13596-024-00794-7","DOIUrl":"10.1007/s13596-024-00794-7","url":null,"abstract":"<div><p>Rice has been reported to possess a variety of biological activities and non-colored rice demonstrates the activities less potent than colored rice. Pathum Thani fragrant rice is new strain non-colored Thai rice that become highly consumed rice. Due to less potent activity, an increase in activity of the non-colored rice is needed to perform. Cereals are rich in active compounds and exhibit a number of activities. To verify whether combination with cereals could enhance the activities of the non colored rice, therefore this study was carried out to determine chemical components, antioxidant and antidiabetic activities of ethanol extracts from Pathum Thani fragrant rice both individual and combination with cereals, compared to those from Black rice. GC-MS analysis revealed the presence of 32, 48, 63, and 66 chemicals in the ethanol extracts from Pathum Thani fragrant rice extract (PTRE), Pathum Thani fragrant rice extract combined with cereals (PTRCE), Black rice extract (BRE), and Black rice extract combined with cereals (BRCE), respectively. The docking study showed that 9-Octadecadienoic acid (Z, Z)-, one of the predominant chemicals in the extracts interacted in the active site pocket of α-glucosidase and α-amylase. PTRE exhibited antioxidant activity by DPPH scavenging activity and antidiabetic activity by inhibiting α-glucosidase activity, increasing body weight and serum insulin levels and reducing blood glucose levels in STZ diabetic rats. Interestingly, PTRCE exerted higher affective activities higher compared to PTRE. The results indicate that Pathum Thani fragrant rice can be enhanced the activities and developed as a therapeutic agent for management of free radical-related diseases and diabetes mellitus, by combination with cereals.</p></div>","PeriodicalId":7613,"journal":{"name":"Advances in Traditional Medicine","volume":"25 2","pages":"509 - 522"},"PeriodicalIF":1.8,"publicationDate":"2024-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144091173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-16DOI: 10.1007/s13596-024-00783-w
Asiat Na’Allah, Simbiat Bashir, Mutiu Alabi, Fatai A. Kareem, Gabriel O. Olaifa, Femi J. Afolabi, Sesan Abiodun Aransiola, Chandra Shekhar Seth, Naga Raju Maddela, Ram Prasad
This study aimed to establish anti-diarrhoea agents, through in vivo and in silico molecular modelling from the phytoconstituents of Citrullus colocynthis ethanol fruit pulp extract (CCEFPE). The crystal structure of µ (mu) opioid and aquaporin 4 (AQP4) receptors were retrieved from the RCSB database, while the identified compounds from C. colocynthis ethanol fruit pulp extract were sequentially docked via Schrödinger suite. In CCEFPE in vivo anti-diarrhoea studies, control received distilled water (2 mL/kg, p.o.), diarrhoea was administered with castor oil or MgSO4 (2 mL/kg, p.o.), standard drug was administered 2 mg/kg, p.o. loperamide, while CCEFPE (50, 100 and 150 mg/kg, p.o.) was administered to the treated groups. Seven hit compounds out of which 54 displayed relatively higher free binding energy for mu opioid and AQP4. Swiss ADME predicted compounds 54 to be blood–brain impermeant, have low gastrointestinal absorption, strong druglike-ness, and safety profile among the hits. In the in vivo study, the onset of diarrhoea was significantly (p < 0.05) delayed by CCEFPE. A significant reduction (p < 0.05) in gastrointestinal motility, enteropooling and PGE2 in diarrhoea-induced groups was also observed after CCEFPE administration. Compound 54, even though it has drug-like properties, displayed a weak interaction with the receptor and hence can be structurally modified to an analogue of loperamide for a better ligand-receptor interaction while the in vivo studies confirmed the anti-diarrhoea activities of C. colocynthis ethanol fruit pulp extract.
{"title":"Anti-diarrhoea properties of ethanol extract of Citrullus colocynthis fruit pulp: in vivo and in silico studies","authors":"Asiat Na’Allah, Simbiat Bashir, Mutiu Alabi, Fatai A. Kareem, Gabriel O. Olaifa, Femi J. Afolabi, Sesan Abiodun Aransiola, Chandra Shekhar Seth, Naga Raju Maddela, Ram Prasad","doi":"10.1007/s13596-024-00783-w","DOIUrl":"10.1007/s13596-024-00783-w","url":null,"abstract":"<div><p>This study aimed to establish anti-diarrhoea agents, through in vivo and in silico molecular modelling from the phytoconstituents of <i>Citrullus colocynthis</i> ethanol fruit pulp extract (CCEFPE). The crystal structure of µ (mu) opioid and aquaporin 4 (AQP4) receptors were retrieved from the RCSB database, while the identified compounds from <i>C. colocynthis</i> ethanol fruit pulp extract were sequentially docked via Schrödinger suite. In CCEFPE in vivo anti-diarrhoea studies, control received distilled water (2 mL/kg, p.o.), diarrhoea was administered with castor oil or MgSO<sub>4</sub> (2 mL/kg, p.o.), standard drug was administered 2 mg/kg, p.o. loperamide, while CCEFPE (50, 100 and 150 mg/kg, p.o.) was administered to the treated groups. Seven hit compounds out of which 54 displayed relatively higher free binding energy for mu opioid and AQP4. Swiss ADME predicted compounds 54 to be blood–brain impermeant, have low gastrointestinal absorption, strong druglike-ness, and safety profile among the hits. In the in vivo study, the onset of diarrhoea was significantly (<i>p</i> < 0.05) delayed by CCEFPE. A significant reduction (<i>p</i> < 0.05) in gastrointestinal motility, enteropooling and PGE<sub>2</sub> in diarrhoea-induced groups was also observed after CCEFPE administration. Compound 54, even though it has drug-like properties, displayed a weak interaction with the receptor and hence can be structurally modified to an analogue of loperamide for a better ligand-receptor interaction while the in vivo studies confirmed the anti-diarrhoea activities of <i>C. colocynthis</i> ethanol fruit pulp extract.</p></div>","PeriodicalId":7613,"journal":{"name":"Advances in Traditional Medicine","volume":"25 1","pages":"269 - 285"},"PeriodicalIF":1.8,"publicationDate":"2024-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143465996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-10-14DOI: 10.1007/s13596-024-00793-8
Amir Hossein Kheirkhah, Maria Kavianpour, Shima Ababzadeh
The fact that cardiovascular diseases have continued to be the top cause of death across the world over the course of many years hammers home the crucial need of discovering breakthrough therapeutic approaches. Stem cell therapy has emerged as a potentially beneficial method due to the fact that it has the ability to boost functional improvement and facilitate the regeneration of tissue. This has led to the application of stem cell therapy by the medical community. On the other hand, its therapeutic efficacy has been impeded by a variety of obstacles, including insufficient engraftment and survival of transplanted cells. These difficulties have made it difficult for it to be effective. In this context, herbal medicine, which has been utilised for a very long time and has a wide variety of bioactive components, presents itself as a powerful instrument that has the potential to enhance stem cell therapy for cardiovascular diseases.
{"title":"Herbal medicine: a potent booster for stem cell therapy in cardiovascular diseases","authors":"Amir Hossein Kheirkhah, Maria Kavianpour, Shima Ababzadeh","doi":"10.1007/s13596-024-00793-8","DOIUrl":"10.1007/s13596-024-00793-8","url":null,"abstract":"<div><p>The fact that cardiovascular diseases have continued to be the top cause of death across the world over the course of many years hammers home the crucial need of discovering breakthrough therapeutic approaches. Stem cell therapy has emerged as a potentially beneficial method due to the fact that it has the ability to boost functional improvement and facilitate the regeneration of tissue. This has led to the application of stem cell therapy by the medical community. On the other hand, its therapeutic efficacy has been impeded by a variety of obstacles, including insufficient engraftment and survival of transplanted cells. These difficulties have made it difficult for it to be effective. In this context, herbal medicine, which has been utilised for a very long time and has a wide variety of bioactive components, presents itself as a powerful instrument that has the potential to enhance stem cell therapy for cardiovascular diseases.</p></div>","PeriodicalId":7613,"journal":{"name":"Advances in Traditional Medicine","volume":"25 2","pages":"395 - 410"},"PeriodicalIF":1.8,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144091054","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
We fabricated silver nanoparticles (AgNPs) using Pterorhachis zenkeri, characterized by Atomic Force Microscopy (AFM) and determined their antioxidant potentials in vitro. Results confirmed the fabrication of AgNPs by using P. zenkeri as a bioreducing agent for the first time. AgNPs possessed potent antioxidant activity in vitro. Furthermore, the TM3 cells were treated for 24 h with AgNPs, vitamin E and cyclophosphamide (CP) at different concentrations (25, 50, 100, 250 and 500 µg/ml). The cells morphology, apoptosis, mitochondrial membrane depolarisation (MMD), Reactive Oxygen Species (ROS), caspase 3/9, oxidative stress-related enzymes, testosterone, and the mRNA expression of steroidogenic acute regulatory protein (StAR) were measured. Results revealed that AgNPs, vitamin E and CP decreased the cell viability in a dose-dependent manner, but did not affect the TM3 cells morphology after treatment. The cytotoxicity of CP in TM3 cells was alleviated after AgNPs application. For instance, AgNPs significantly (p < 0.001–0.05) reduced the MMD, ROS production, and caspase 3/9 activities, but increased the activities of superoxide dismutase, catalase and glutathione peroxidase in the TM3 cells. Moreover, AgNPs improved testosterone production by activating StAR machineries. These results indicate that AgNPs/P. zenkeri could be a potential alternative drug in the management of oxidative stress and androgen deficit associated with CP chemotherapy.
{"title":"Biosynthesis of silver nanoparticles using Pterorhachis zenkeri: characterization and evaluation of antioxidant, anti-apoptotic, and androgenic properties in TM3 leydig cells exposed to cyclophosphamide","authors":"Patrick Brice Defo Deeh, Nagabhishek Sirpu Natesh, Karthik Alagarsamy, Madan Kumar Arumugam, Ramachandran Dasnamoorthy, Tharunkumar Sivaji, Vinita Vishwakarma","doi":"10.1007/s13596-024-00792-9","DOIUrl":"10.1007/s13596-024-00792-9","url":null,"abstract":"<div><p>We fabricated silver nanoparticles (AgNPs) using <i>Pterorhachis zenkeri</i>, characterized by Atomic Force Microscopy (AFM) and determined their antioxidant potentials in vitro. Results confirmed the fabrication of AgNPs by using <i>P. zenkeri</i> as a bioreducing agent for the first time. AgNPs possessed potent antioxidant activity <i>in vitro.</i> Furthermore, the TM3 cells were treated for 24 h with AgNPs, vitamin E and cyclophosphamide (CP) at different concentrations (25, 50, 100, 250 and 500 µg/ml). The cells morphology, apoptosis, mitochondrial membrane depolarisation (MMD), Reactive Oxygen Species (ROS), caspase 3/9, oxidative stress-related enzymes, testosterone, and the mRNA expression of steroidogenic acute regulatory protein (StAR) were measured. Results revealed that AgNPs, vitamin E and CP decreased the cell viability in a dose-dependent manner, but did not affect the TM3 cells morphology after treatment. The cytotoxicity of CP in TM3 cells was alleviated after AgNPs application. For instance, AgNPs significantly (<i>p</i> < 0.001–0.05) reduced the MMD, ROS production, and caspase 3/9 activities, but increased the activities of superoxide dismutase, catalase and glutathione peroxidase in the TM3 cells. Moreover, AgNPs improved testosterone production by activating StAR machineries. These results indicate that AgNPs/<i>P. zenkeri</i> could be a potential alternative drug in the management of oxidative stress and androgen deficit associated with CP chemotherapy.</p></div>","PeriodicalId":7613,"journal":{"name":"Advances in Traditional Medicine","volume":"25 2","pages":"495 - 508"},"PeriodicalIF":1.8,"publicationDate":"2024-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144091127","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A never-ending search is being made for a natural remedy to cure diabetes, which is one of the biggest worldwide health concerns. Kaempferia galanga (K. galanga), an important medicinal herb, is reported to have various pharmacological effects. This study aims to conduct in-depth research on the antihyperglycemic activity of K galanga in streptozotocin (STZ)-induced diabetic mice and the mechanism by which it elicits its response. For 21 days, various dosages of freeze-dried K. galanga ethanolic extract (KGE) therapy were given intraperitoneally in STZ-induced diabetic mice. KGE at 350 mg/kg b.w. was selected as the ideal dose. Acute toxicology studies have shown that KGE is non-toxic. Protein and gene expression studies targeting various metabolic pathways show that in the diabetic mice treated with KGE, there was stimulation of AKT, inhibition of glycogen synthase kinase-3, stimulation of glucokinase (GK), and inhibition of phosphoenolpyruvate carboxykinase (PEPCK) expression. Histopathological studies show the protective effect of herbal KGE on the integrity of the mice's pancreas. Molecular docking studies was performed in which the bio-active compound ethyl-p-methoxy cinnamate (EPMC) found in KGE shows good binding energy with the target protein AKT, GSK3, insulin receptor (IR), protein-tyrosine phosphatase 1B (PTB1B), GK, and PEPCK, indicating a good binding interaction. ADMET studies also revealed that EPMC has desirable physicochemical and pharmacokinetic properties and very low toxicity (LD 50 7900 mg/kg) compared to standard metformin (LD50 680 mg/kg). Herbal KGE and EPMC show a pleiotropic therapeutic effect and may be a potent adjunct and drug, respectively, in attenuating diabetes.