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1.
Tech Coloproctol ; 27(12): 1335-1343, 2023 12.
Artigo em Inglês | MEDLINE | ID: mdl-37848640

RESUMO

BACKGROUND: Aluminum potassium sulfate and tannic acid (ALTA) is an effective sclerosing agent for the treatment of internal hemorrhoids. ALTA therapy with rectal mucopexy (AM) is a new approach for treating hemorrhoidal prolapse. This study investigated the midterm outcomes of AM surgery in patients with hemorrhoids. METHODS: Patients with grade III hemorrhoids who underwent AM surgery were enrolled in this retrospective analysis of prospectively collected data from a single institution. Cumulative success rates, postoperative symptoms, including pain scores, analgesic requirements, and postoperative complications, and patient satisfaction were assessed. RESULTS: The median number of ALTA injection procedures was 3 (range 1-4), and the median total injection dose was 19 mL (range 7-32 mL). The median number of mucopexy procedures was 2 (range 1-4). The median postoperative pain score (0 = no pain at all, 10 = worst pain imaginable) at rest or during defecation were ≤2. The total dose of analgesics administered during the first two weeks after surgery was 1 (range 0-25). Six patients (5.3%) showed postoperative complications: five showed Clavien-Dindo (C-D) grade I and one showed C-D grade IIIa complications. Cumulative success rates at one, three, and five years were 96.5%, 85.3%, and 85.3%, respectively. Patient satisfaction scores, which were assessed using a 10-point scale, were ≥9 at each postoperative year. CONCLUSIONS: AM surgery is an effective non-excisional surgery with satisfactory mid-term results for grade III hemorrhoids, and is associated with lower complication rates, postoperative analgesic requirements, and higher patient satisfaction.


Assuntos
Hemorroidas , Humanos , Hemorroidas/cirurgia , Escleroterapia , Estudos Retrospectivos , Dor Pós-Operatória/etiologia , Dor Pós-Operatória/tratamento farmacológico , Ligadura/métodos , Taninos/efeitos adversos , Analgésicos/uso terapêutico , Resultado do Tratamento
2.
Int Immunopharmacol ; 110: 108970, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-35792271

RESUMO

Tannic acid (TA) is a natural compound present abundantly in fruit such as grapes and green tea. In this study, we have evaluated the therapeutic efficacy of TA against Lipopolysaccharide (LPS)-induced oxidative stress-mediated memory impairment, neuroinflammation, insulin signaling impairment, and Amyloid Beta (Aß) deposition in adult male mice. The LPS was administered once per week and TA twice a week to adult male mice for three months consecutively. Behavioral studies were performed using different behavioral models such as balance beam, novel object recognition (NOR), Morris water maze (MWM), and Y-maze tests. The protein expression of different mediators such as TNF-α, p-JNK, pIRS636, BACE1, APP, and Aß was evaluated through western blot and immunofluorescence staining techniques. Biochemical assays were carried out to assess the antioxidant activities of TA. The computational study was conducted to predict the binding mode of TA with target sites of TNF-α. Behavioral studies showed that the TA-treated mice exhibited gradual memory improvement. TA significantly inhibited BACE1 activity and reduced production and accumulation of Aß in the hippocampus of mice brains. Moreover, the TA significantly inhibited LPS-induced ROS production and enhanced the glutathione levels. Furthermore, we have shown via the computational method for the first time that TA inhibits LPS-triggered TNF-á½° and its downstream signaling to reduce AD pathology including memory impairment, neuroinflammation, insulin signaling impairment, and Aß deposition in adult mice. Taken together our current study demonstrates that TA is a potential candidate for the abrogation of LPS-induced neurotoxicity and AD pathology in rodent's models.


Assuntos
Doença de Alzheimer , Disfunção Cognitiva , Insulinas , Secretases da Proteína Precursora do Amiloide/metabolismo , Peptídeos beta-Amiloides/metabolismo , Animais , Ácido Aspártico Endopeptidases/efeitos adversos , Ácido Aspártico Endopeptidases/metabolismo , Disfunção Cognitiva/induzido quimicamente , Disfunção Cognitiva/tratamento farmacológico , Disfunção Cognitiva/metabolismo , Modelos Animais de Doenças , Insulinas/efeitos adversos , Lipopolissacarídeos/farmacologia , Masculino , Aprendizagem em Labirinto , Transtornos da Memória/induzido quimicamente , Transtornos da Memória/tratamento farmacológico , Transtornos da Memória/metabolismo , Camundongos , Taninos/efeitos adversos , Fator de Necrose Tumoral alfa/metabolismo
3.
Cardiovasc Hematol Agents Med Chem ; 20(3): 197-211, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35538824

RESUMO

AIMS: The study aimed to assess the antihyperglycemic activity of Pulicaria mauritanica. BACKGROUND: Pulicaria mauritanica is a medicinal and aromatic plant used for the treatment of many diseases such as inflammation, diabetes, and intestinal disorders. OBJECTIVE: The main goals of this present paper were to confirm the antihyperglycemic capacity of aqueous extract from Pulicaria mauritanica in normoglycemic and diabetic rats over a period of time (7 days of treatment). METHODS: The effect of the aqueous extract of Pulicaria mauritanica from aerial parts (AEPM) on glucose and lipid metabolism was tested using an acute test (single dose during 6 hours) and subchronic assay (repeated oral administration for seven days) at a dose of 60 mg/kg and the serum glucose levels were measured in normoglycemic and streptozotocin(STZ)-induced diabetic rats. In addition, the glycogen content in the liver, extensor digitorum longus (EDL), and soleus was evaluated. The antioxidant activity, phytochemical screening, and quantification of some secondary metabolites of this extract were also performed. RESULTS: AEPM at a dose of 60 mg/kg reduced the plasma glucose concentrations significantly in STZ-induced diabetic rats after a single oral administration (p<0.05). This lowering effect became more significant during the repeated oral administration in hyperglycemic rats (p<0.0001). Also, the findings showed that this plant exhibited a significant increase in liver and skeletal soleus muscle glycogen content in diabetic rats. AEPM revealed a remarkable antioxidant activity in addition to the presence of polyphenol compounds such as flavonoids, tannins, saponins, sterols, glucides, terpenoids, quinones, anthraquinones, and mucilage. CONCLUSION: The study shows that AEPM exhibits antihyperglycemic activity in diabetic rats, and it increases liver and muscle glycogen content.


Assuntos
Diabetes Mellitus Experimental , Pulicaria , Saponinas , Animais , Antraquinonas/efeitos adversos , Antioxidantes/uso terapêutico , Glicemia , Flavonoides/uso terapêutico , Glucose/metabolismo , Glicogênio/efeitos adversos , Glicogênio/metabolismo , Hipoglicemiantes/farmacologia , Hipoglicemiantes/uso terapêutico , Extratos Vegetais/química , Polifenóis/efeitos adversos , Pulicaria/metabolismo , Quinonas/efeitos adversos , Ratos , Ratos Wistar , Saponinas/efeitos adversos , Esteróis , Estreptozocina , Taninos/efeitos adversos , Terpenos/efeitos adversos
4.
Trials ; 22(1): 310, 2021 Apr 28.
Artigo em Inglês | MEDLINE | ID: mdl-33910614

RESUMO

OBJECTIVES: This research aims to study the efficacy of tannins co-supplementation on disease duration, severity and clinical symptoms, microbiota composition and inflammatory mediators in SARS-CoV2 patients. TRIAL DESIGN: This is a prospective, double-blind, randomized, placebo-controlled, parallel-group trial to evaluate the efficacy of the administration of the dietary supplement ARBOX, a molecular blend of quebracho and chestnut tannins extract and Vit B12, in patients affected by COVID-19. PARTICIPANTS: 18 years of age or older, admitted to Hospital de Clinicas Jose de San Martin, Buenos Aires University (Argentina), meeting the definition of "COVID-19 confirmed case" ( https://www.argentina.gob.ar/salud/coronavirus-COVID-19/definicion-de-caso ). Inclusion Criteria Participants are eligible to be included in the study if the following criteria apply: 1. Any gender 2. ≥18 years old 3. Informed consent for participation in the study 4. Virological diagnosis of SARS-CoV-2 infection (real-time PCR) Exclusion Criteria Participants are excluded from the study if any of the following criteria apply: 1. Pregnant and lactating patients 2. Patients who cannot take oral therapy (with severe cognitive decline, assisted ventilation, or impaired consciousness) 3. Hypersensitivity to polyphenols 4. Patients already in ICU or requiring mechanical ventilation 5. Patients already enrolled in other clinical trials 6. Decline of consent INTERVENTION AND COMPARATOR: Experimental: TREATED ARM Participants will receive a supply of 28 -- 390 mg ARBOX capsules for 14 days. Patients will be supplemented with 2 capsules of ARBOX per day. Placebo Comparator: CONTROL ARM Participants will receive placebo supply for 14 days. The placebo will be administered with the identical dose as described for the test product. All trial participants will receive standard therapy, which includes: Antipyretics or Lopinavir / Ritonavir, Azithromycin and Hydroxychloroquine, as appropriate (treatment currently recommended by the department of Infectious Diseases of the Hospital de Clínicas that could undergo to modifications). In addition, if necessary: supplemental O2, non-invasive ventilation, antibiotic therapy. MAIN OUTCOMES: Primary Outcome Measures: Time to hospital discharge, defined as the time from first dose of ARBOX to hospital discharge [ Time Frame: Throughout the Study (Day 0 to Day 28) ] Secondary Outcome Measures: 28-day all-cause mortality [ Time Frame: Throughout the Study (Day 0 to Day 28) ]-proportion Invasive ventilation on day 28 [ Time Frame: Throughout the Study (Day 0 to Day 28) ]-proportion Level of inflammation parameters and cytokines [ Time Frame: day 1-14 ] -mean difference Difference in fecal intestinal microbiota composition and intestinal permeability [ Time Frame: day 1-14 ] Negativization of COVID-PCR at day 14 [ Time Frame: day 14 ]-proportion RANDOMIZATION: Potential study participants were screened for eligibility 24 hours prior to study randomization. Patients were randomly assigned via computer-generated random numbering (1:1) to receive standard treatment coupled with tannin or standard treatment plus placebo (control group). BLINDING (MASKING): Study personnel and participants are blinded to the treatment allocation, as both ARBOX and placebo were packed in identical containers. Thus, all the used capsules had identical appearance. NUMBERS TO BE RANDOMIZED (SAMPLE SIZE): Considering an alpha error of 5%, a power of 80% a sample size of 70 patients per branch was estimated. 140 patients in total. TRIAL STATUS: The protocol version is number V2, dated May 23, 2020. The first patient, first visit was on June 12, 2020; the recruitment end date was October 6, 2020. The protocol was not submitted earlier because the enrollment of some patients took place after the closure of the recruitment on the clinicaltrials platform. In fact, due to the epidemiological conditions, due to the decrease of the cases in Argentina during the summer period, the recruitment stopped t before reaching the number of 140 patients (as indicated in the webpage). However, since there was a new increase in cases, the enrolment was resumed in order to reach the number of patients initially planned in the protocol. The final participant was recruited on February 14, 2021. TRIAL REGISTRATION: ClinicalTrials.gov, number: NCT04403646 , registered on May 27th, 2020. FULL PROTOCOL: The full protocol is attached as an additional file, accessible from the Trials website (Additional file 1). In the interest in expediting dissemination of this material, the familiar formatting has been eliminated; this Letter serves as a summary of the key elements of the full protocol.


Assuntos
COVID-19 , Adolescente , Adulto , Argentina , Suplementos Nutricionais , Feminino , Humanos , Lactação , Extratos Vegetais/efeitos adversos , Gravidez , Estudos Prospectivos , RNA Viral , Ensaios Clínicos Controlados Aleatórios como Assunto , SARS-CoV-2 , Taninos/efeitos adversos , Resultado do Tratamento
5.
Asian J Endosc Surg ; 12(4): 473-477, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-30411508

RESUMO

Aluminum potassium sulfate and tannic acid (ALTA) injection is a new sclerosing therapy for internal hemorrhoids that has been gaining widespread use. However, there have been few reports about rectal cancer after ALTA injection. We performed laparoscopic surgery for three patients who had underwent ALTA therapy 6 months or 1 year earlier: (i) a 51-year-old man with neuroendocrine tumor; (ii) a 44-year-old woman with rectal cancer; and (iii) 77-year-old man with rectal cancer. All three patients had sclerosis of the resected rectal wall stump, making transection of the rectum difficult. Histological examination of the specimens also showed an inflammatory reaction and/or fibrosis of the resection stump. Although laparoscopic low anterior resection was planned for all three patients, we had to construct a diverting stoma for two patients and could not perform sphincter-preserving surgery for the other. We must be well prepared for laparoscopic rectal surgeries after ALTA therapy, and these cases suggest sigmoidoscopy before ALTA therapy should be recommended.


Assuntos
Hemorroidas/tratamento farmacológico , Laparoscopia , Neoplasias Retais/induzido quimicamente , Neoplasias Retais/cirurgia , Soluções Esclerosantes/efeitos adversos , Adulto , Idoso , Compostos de Alúmen/efeitos adversos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Taninos/efeitos adversos
6.
Regul Toxicol Pharmacol ; 92: 182-188, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-29233773

RESUMO

Terminalia chebula fruits are one of the richest sources of hydrolysable tannins and it is well known medicinal agent in traditional systems of medicine for treatment of various chronic ailments. In the present study, hydrolysable tannin rich fraction (HTF) was isolated from 80% hydroalcoholic extract of Terminalia chebula fruit pericarps and it was studied for acute and repeated dose oral toxicity in Wistar albino rats. HTF did not show any toxic symptoms or mortality at single dose administration of 5000 mg/kg/p.o followed by observation for 14 days. On repeated dose 28 days oral toxicity study, administration of HTF at 1000 mg/kg showed marked reduction in body weight, food intake and water intake when compared with vehicle control. It was also observed that HTF could increase serum urea, glucose and AST level significantly when compared with vehicle control indicating mild disturbances in liver and kidney functions. On histopathological screening, HTF treatment showed a mild granulomatous inflammation in the liver and all other organs remained normal. It was concluded that following 28 days repeated dose oral administration, HTF caused mild disturbances in liver and kidney function which was indicated by reduced body weight, food and water intake, serum parameters and histological observations.


Assuntos
Frutas/efeitos adversos , Extratos Vegetais/administração & dosagem , Extratos Vegetais/efeitos adversos , Taninos/administração & dosagem , Taninos/efeitos adversos , Terminalia/efeitos adversos , Administração Oral , Animais , Feminino , Aromatizantes/efeitos adversos , Rim/efeitos dos fármacos , Fígado/efeitos dos fármacos , Ratos , Ratos Wistar , Testes de Toxicidade/métodos
7.
Expert Rev Gastroenterol Hepatol ; 12(1): 83-90, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28946778

RESUMO

INTRODUCTION: The intestinal barrier controls the absorption of nutrients and water whilst helping to prevent the entry of toxins and pathogenic micro-organisms from the lumen into the tissues. Deficiencies in the barrier are associated with various gastrointestinal and extra digestive disorders. Areas covered: This review provides an overview of the relationship between increased intestinal permeability and disease, and considers the role of mucosal protectants (mucoprotectants) in restoring normal intestinal barrier function, with a particular focus on diarrheal disorders. Expert commentary: Impairment of the intestinal barrier characterizes a variety of diseases, and there is ongoing interest in the development of pharmacological approaches targeting the reduction of intestinal permeability. These include corticosteroids, aminosalicylates and anti-tumor necrosis factor-α (TNF-α), which act by reducing inflammation; probiotics, which modulate the production of mucin and epithelial tight junction proteins; and mucoprotectants, which form a protective film over the epithelium. Recently, preclinical and clinical data highlight, the ability of new mucoprotectants, such as gelatin tannate and xyloglucan, to protect the intestinal mucosa and to exert anti-diarrheal effects. In the future the ability of these substances to enhance the intestinal barrier may extend their use in the management of a variety of gastro-intestinal diseases associated with 'leaky gut'.


Assuntos
Demulcentes/uso terapêutico , Diarreia/tratamento farmacológico , Gelatina/uso terapêutico , Glucanos/uso terapêutico , Doenças Inflamatórias Intestinais/tratamento farmacológico , Absorção Intestinal/efeitos dos fármacos , Mucosa Intestinal/efeitos dos fármacos , Taninos/uso terapêutico , Xilanos/uso terapêutico , Demulcentes/efeitos adversos , Diarreia/diagnóstico , Diarreia/metabolismo , Diarreia/fisiopatologia , Gelatina/efeitos adversos , Glucanos/efeitos adversos , Humanos , Doenças Inflamatórias Intestinais/diagnóstico , Doenças Inflamatórias Intestinais/metabolismo , Doenças Inflamatórias Intestinais/fisiopatologia , Mucosa Intestinal/metabolismo , Mucosa Intestinal/patologia , Mucosa Intestinal/fisiopatologia , Permeabilidade , Taninos/efeitos adversos , Resultado do Tratamento , Xilanos/efeitos adversos
8.
World J Gastroenterol ; 23(27): 5034-5040, 2017 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-28785156

RESUMO

We are reporting a rare case of acute liver injury that developed after an internal hemorrhoid treatment with the aluminum potassium sulfate and tannic acid (ALTA) regimen. A 41-year-old man developed a fever and liver injury after undergoing internal hemorrhoid treatment with a submucosal injection of ALTA with lidocaine. The acute liver injury was classified clinically as hepatocellular and pathologically as cholestastic. We could not classify the mechanism of injury. High eosinophil and immunoglobulin E levels characterized the injury, and a drug lymphocyte stimulation test was negative on postoperative day 25. Fluid replacement for two weeks after hospitalization improved the liver injury. ALTA therapy involves injecting chemicals into the submucosa, from the rectum to the anus, and this is the first description of a case that developed a severe liver disorder after this treatment; hence, an analysis of future cases as they accumulate is desirable.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/etiologia , Hemorroidas/terapia , Injeções Intralesionais/efeitos adversos , Soluções Esclerosantes/efeitos adversos , Escleroterapia/efeitos adversos , Adulto , Compostos de Alúmen/administração & dosagem , Compostos de Alúmen/efeitos adversos , Doença Hepática Induzida por Substâncias e Drogas/sangue , Febre/sangue , Febre/etiologia , Humanos , Lidocaína/administração & dosagem , Lidocaína/efeitos adversos , Fígado/efeitos dos fármacos , Testes de Função Hepática , Masculino , Complicações Pós-Operatórias/sangue , Complicações Pós-Operatórias/etiologia , Soluções Esclerosantes/administração & dosagem , Escleroterapia/métodos , Taninos/administração & dosagem , Taninos/efeitos adversos
10.
Physiol Behav ; 163: 56-63, 2016 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-27129672

RESUMO

Salivary protein difference value (SP D-value) is a quantitative measure of salivary protein replenishment, which reportedly relates to individual differences in perceived astringency. This in vitro measure is calculated as the difference in total salivary protein before (S1) and after (S2) stimulation with tannic acid, with a greater absolute value (S2-S1) indicating less protein replenishment. Others report that this measure predicts perceived astringency and liking of liquid model systems and beverages containing added polyphenols. Whether this relationship generalizes to astringent compounds other than polyphenols, or to solid foods is unknown. Here, the associations between SP D-values and perceived astringency and overall liking/disliking for alum and tannic acid (experiment 1) as well as solid chocolate-flavored compound coating with added tannic acid or grape seed extract (GSE) (experiment 2) were examined. In both experiments, participants (n=84 and 81, respectively) indicated perceived intensity of astringency, bitterness, sweetness, and sourness, and degree of liking of either aqueous solutions, or solid chocolate-flavored compound coating with added astringents. Data were analyzed via linear regression, and as discrete groups for comparison to prior work. Three discrete groups were formed based on first and third quartile splits of the SP D-value distribution: low (LR), medium (MR), and high responding (HR) individuals. In experiment 1, significantly higher mean astringency ratings were observed for the HR as compared to the LR/MR groups for alum and tannic acid, confirming and extending prior work. In experiment 2, significantly higher mean astringency ratings were also observed for HR as compared to LR groups in solid chocolate-flavored compound containing added tannic acid or GSE. Significant differences in liking were found between HR and LR groups for alum and tannic acid in water, but no significant differences in liking were observed for chocolate-flavored compound samples. A significant linear relationship between SP D-values and perceived astringency was observed for both alum and tannic acid (p's<0.001), although the variance explained was relatively low (R(2)=0.33 and 0.29, respectively). In the solid chocolate-flavored compound spiked with either tannic acid or GSE, the relationship was not significant (p=0.17 and 0.30; R(2)=0.03 and 0.02, respectively). Due to the weak associations overall, and the lack of significant differences in perception of astringency between the MR and LR groups, we conclude that SP D-values are not a strong predictor of astringency, especially in solid, high-fat foods. Additional research investigating alternative methods for quantifying individual differences in astringency, as well as exploring the underlying complexities of this percept appears warranted.


Assuntos
Adstringentes/efeitos adversos , Saliva/metabolismo , Proteínas e Peptídeos Salivares/metabolismo , Percepção Gustatória/efeitos dos fármacos , Paladar/efeitos dos fármacos , Percepção do Tato/fisiologia , Adolescente , Adulto , Compostos de Alúmen/efeitos adversos , Relação Dose-Resposta a Droga , Feminino , Voluntários Saudáveis , Humanos , Masculino , Pessoa de Meia-Idade , Modelos Biológicos , Análise de Regressão , Taninos/efeitos adversos , Percepção Gustatória/fisiologia , Adulto Jovem
11.
Nutr Neurosci ; 19(6): 269-78, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25842984

RESUMO

BACKGROUND/AIMS: Emblica officinalis is mentioned as a maharasayana in many Ayurvedic texts and promotes intelligence, memory, freedom from disease, longevity, and strength of the senses. The present study has been designed to explore the memory-enhancing effect of the tannoid principles of E. officinalis (EoT) at the biochemical, anatomical, behavioral, and molecular levels against aluminum chloride (AlCl3) induced Alzheimer's disease (AD) in rats. Aluminum is reported to have an important role in the etiology, pathogenesis, and development of AD. METHODS: Male Wistar rats were divided into control, AlCl3 treated, AlCl3 and EoT (50, 100, and 200 mg/kg bw) co-treated, and EoT (200 mg/kg bw) alone treated groups. In control and experimental rats, behavior tests including water maze and open field test, estimation of aluminum, assay of acetylcholinesterase (AChE) activity, and expression of amyloidogenic proteins were performed. RESULTS: Intraperitonial injection of AlCl3 (100 mg/kg bw) for 60 days significantly elevated the concentration of aluminum (Al), activity of AChE and protein expressions of amyloid precursor protein, A-beta1-42, beta-, and gamma-secretases as compared to control group in hippocampus and cortex. Co-administration of EoT orally to AlCl3 rats for 60 days significantly revert back the Al concentration, AChE activity, and A-beta synthesis-related molecules in the studied brain regions. The spatial learning, memory, and locomotor impairments observed in AlCl3 treated rats were significantly attenuated by EoT. CONCLUSION: Therefore, EoT may be a promising therapy in ameliorating neurotoxicity of aluminum, however further studies are warranted to elucidate the exact mechanism of action of EoT.


Assuntos
Doença de Alzheimer/prevenção & controle , Disfunção Cognitiva/prevenção & controle , Modelos Animais de Doenças , Fármacos Neuroprotetores/uso terapêutico , Phyllanthus emblica/química , Extratos Vegetais/uso terapêutico , Placa Amiloide/prevenção & controle , Cloreto de Alumínio , Compostos de Alumínio , Doença de Alzheimer/metabolismo , Doença de Alzheimer/patologia , Doença de Alzheimer/fisiopatologia , Animais , Biomarcadores/metabolismo , Córtex Cerebral/metabolismo , Córtex Cerebral/patologia , Cloretos , Disfunção Cognitiva/etiologia , Suplementos Nutricionais/análise , Etnofarmacologia , Frutas/química , Hipocampo/metabolismo , Hipocampo/patologia , Masculino , Ayurveda , Proteínas do Tecido Nervoso/metabolismo , Neurônios/metabolismo , Neurônios/patologia , Fármacos Neuroprotetores/administração & dosagem , Fármacos Neuroprotetores/efeitos adversos , Fármacos Neuroprotetores/química , Extratos Vegetais/administração & dosagem , Extratos Vegetais/efeitos adversos , Extratos Vegetais/química , Placa Amiloide/etiologia , Distribuição Aleatória , Ratos Wistar , Taninos/administração & dosagem , Taninos/efeitos adversos , Taninos/análise , Taninos/uso terapêutico
12.
Food Chem Toxicol ; 84: 37-46, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26231140

RESUMO

In this study we compared the antioxidant and DNA protective activity of tannic acid and stilbene derivatives, resveratrol, 3,5,4(')-trimethoxystilbene (TMS) and pterostilbene in human neutrophils stimulated to oxidative burst by 12-O-tetradecanoyl-phorbol-13-acetate (TPA) in relation to apoptosis induction. All polyphenols within the concentration range 1-100 µM reduced the intracellular ROS and H2O2 production in the TPA-stimulated cells. Tannic acid was the most effective polyphenol in protection against DNA damage induced by TPA. In the resting neutrophils resveratrol and to lesser extent other polyphenols increased DNA damage and increased the level of p53. Pretreatment of the TPA-stimulated cells with tannic acid or stilbenes led to the induction of apoptosis. The most significant effect was observed as a result of treatment with TMS and resveratrol. These compounds appeared the most effective inducers of p53 in the TPA-challenged neutrophils, what may suggest that pro-apoptotic activity of these stilbenes might be related to p53 activation. Overall, the results of our present study demonstrate that tannic acid and stilbenes modulate the ROS production, ultimately leading to cell apoptosis in human neutrophils stimulated to oxidative burst. In resting neutrophils they exhibit pro-oxidant activity, which is accompanied by p53 induction.


Assuntos
Apoptose , Dano ao DNA , Ativação de Neutrófilo , Neutrófilos/metabolismo , Oxidantes/efeitos adversos , Estilbenos/efeitos adversos , Taninos/efeitos adversos , Anti-Inflamatórios não Esteroides/efeitos adversos , Anti-Inflamatórios não Esteroides/metabolismo , Antioxidantes/efeitos adversos , Antioxidantes/metabolismo , Apoptose/efeitos dos fármacos , Biomarcadores/metabolismo , Carcinógenos/antagonistas & inibidores , Carcinógenos/toxicidade , Células Cultivadas , Humanos , Peróxido de Hidrogênio/antagonistas & inibidores , Peróxido de Hidrogênio/metabolismo , Ativação de Neutrófilo/efeitos dos fármacos , Neutrófilos/citologia , Neutrófilos/efeitos dos fármacos , Neutrófilos/imunologia , Oxidantes/metabolismo , Estresse Oxidativo/efeitos dos fármacos , Espécies Reativas de Oxigênio/antagonistas & inibidores , Espécies Reativas de Oxigênio/metabolismo , Resveratrol , Estilbenos/metabolismo , Taninos/metabolismo , Acetato de Tetradecanoilforbol/antagonistas & inibidores , Acetato de Tetradecanoilforbol/toxicidade , Proteína Supressora de Tumor p53/agonistas , Proteína Supressora de Tumor p53/metabolismo
13.
Planta Med ; 80(12): 1045-50, 2014 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25089737

RESUMO

Inhibition of the human ether-a-go-go-related gene channel is the single most important risk factor leading to acquired long QT syndrome. Drug-induced QT prolongation can cause severe cardiac complications, including arrhythmia, and is thus a liability in drug development. Considering the importance of the human ether-a-go-go-related gene channel as an antitarget and the daily intake of plant-derived foods and herbal products, surprisingly few natural products have been tested for channel blocking properties. In an assessment of possible human ether-a-go-go-related gene liabilities, a selection of widely used herbal medicines and edible plants (vegetables, fruits, and spices) was screened by means of a functional two-microelectrode voltage-clamp assay with Xenopus oocytes. The human ether-a-go-go-related gene channel blocking activity of selected extracts was investigated with the aid of a high-performance liquid chromatography-based profiling approach, and attributed to tannins and alkaloids. Major European medicinal plants and frequently consumed food plants were found to have a low risk for human ether-a-go-go-related gene toxicity.


Assuntos
Arritmias Cardíacas/induzido quimicamente , Canais de Potássio Éter-A-Go-Go/antagonistas & inibidores , Sistema de Condução Cardíaco/anormalidades , Extratos Vegetais/farmacologia , Plantas Comestíveis/química , Plantas Medicinais/química , Bloqueadores dos Canais de Potássio/farmacologia , Alcaloides/efeitos adversos , Alcaloides/farmacologia , Animais , Produtos Biológicos , Síndrome de Brugada , Doença do Sistema de Condução Cardíaco , Medicina Herbária , Humanos , Oócitos , Extratos Vegetais/efeitos adversos , Bloqueadores dos Canais de Potássio/efeitos adversos , Taninos/efeitos adversos , Taninos/farmacologia , Xenopus
14.
Surg Today ; 44(12): 2314-7, 2014 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24817127

RESUMO

PURPOSE: Aluminum potassium sulfate and tannic acid (ALTA) is an effective sclerosing agent for internal hemorrhoids. However, it is contraindicated for patients with chronic renal failure on dialysis, because the aluminum in ALTA can cause aluminum encephalopathy when it is not excreted effectively. We conducted this study to measure the serum aluminum concentrations and observe for symptoms relating to aluminum encephalopathy in dialysis patients after ALTA therapy. METHODS: Ten dialysis patients underwent ALTA therapy for hemorrhoids. We measured their serum aluminum concentrations and observed them for possible symptoms of aluminum encephalopathy. RESULTS: The total injection volume of ALTA solution was 31 mL (24-37). The median serum aluminum concentration before ALTA therapy was 9 µg/L, which increased to 741, 377, and 103 µg/L, respectively, 1 h, 1 day, and 1 week after ALTA therapy. These levels decreased rapidly, to 33 µg/L by 1 month and 11 µg/L by 3 months after ALTA therapy. No patient suffered symptoms related to aluminum encephalopathy. CONCLUSIONS: Although the aluminum concentrations increased temporarily after ALTA therapy, dialysis patients with levels below 150 µg/L by 1 week and thereafter are considered to be at low risk of the development of aluminum encephalopathy.


Assuntos
Compostos de Alúmen/efeitos adversos , Alumínio/sangue , Diálise , Hemorroidas/terapia , Falência Renal Crônica/complicações , Síndromes Neurotóxicas/diagnóstico , Síndromes Neurotóxicas/etiologia , Soluções Esclerosantes/efeitos adversos , Escleroterapia , Taninos/efeitos adversos , Idoso , Idoso de 80 Anos ou mais , Compostos de Alúmen/administração & dosagem , Biomarcadores/sangue , Contraindicações , Feminino , Hemorroidas/complicações , Humanos , Masculino , Pessoa de Meia-Idade , Risco , Soluções Esclerosantes/administração & dosagem , Taninos/administração & dosagem
15.
G Ital Med Lav Ergon ; 34(1): 19-23, 2012.
Artigo em Italiano | MEDLINE | ID: mdl-22697026

RESUMO

Work exposure to carcinogenic chemicals in the shoe industry is still debated owing to continuous technological developments. A possible causal role in sino-nasal cancer development was attributed to the leather dusts basing on epidemiologic studies. Nevertheless, convincing conclusions regarding toxicodinamic-involved processes are actually missing. An hypothesis pointing on tannins toxic action shows insufficient and contrasting data. A cancerogenic risk seems to be attributable for workers engaged in the whole process of shoe industry.


Assuntos
Poeira , Doenças Profissionais/induzido quimicamente , Neoplasias dos Seios Paranasais/induzido quimicamente , Humanos , Itália/epidemiologia , Doenças Profissionais/epidemiologia , Neoplasias dos Seios Paranasais/epidemiologia , Taninos/efeitos adversos
16.
J Ethnopharmacol ; 143(1): 185-93, 2012 Aug 30.
Artigo em Inglês | MEDLINE | ID: mdl-22732728

RESUMO

ETHNOPHARMACOLOGY RELEVANCE: Several ailments are caused by infectious bacteria and in other diseases; they act as co-infection which complicate human life by causing health hazards. In Venda (South Africa), many plants are used in traditional medicine to treat cough and fever. AIM OF THE STUDY: This study was aimed at evaluating the antibacterial and antifungal properties, cyclooxygenases (COX), acetylcholinesterase (AChE) enzyme inhibitory effects and the phenolic composition as well as mutagenic properties of six medicinal plants used by the Venda people of Limpopo Province of South Africa against cough and fever. MATERIALS AND METHODS: The petroleum ether (PE), dichloromethane (DCM), 80% ethanol (EtOH) and water extracts of six plants were tested against four infectious bacteria (Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae and Staphylococcus aureus) and a fungus Candida albicans. The same extracts were evaluated for their ability to inhibit COX-1 and -2 enzymes. Methanolic and water extracts of the same plant were tested for acetylcholinesterase inhibitory effects. Total phenolics, flavonoids, gallotannins and condensed tannins were determined. The ability of the extracts to bind and precipitate proteins was also investigated. The extracts were investigated for genotoxicity with and without S9 (metabolic activation) against three Salmonella typhimurium tester strains TA98, TA100 and TA102. RESULTS: The organic extracts of Rhus lancea leaves exhibited the best antibacterial activity with minimum inhibitory concentration (MIC) values ranging from 0.0061 to 0.049mg/ml. The best antifungal activity was observed from a DCM extract of Syzygium cordatum leaves with a MIC value of 0.195mg/ml. The methanolic and water extracts of the same plant exhibited high inhibitory effects towards AChE with IC(50) values of 0.22 and 0.26mg/ml, respectively. The highest levels of flavonoids and gallotannins were detected in Spirostachys africana bark; 11.57 and 48.88µg/g, respectively. The highest percentages (1.2%) of condensed tannins were detected in Uvaria caffra leaves. The high levels of phenolic compounds may have been responsible for high antimicrobial activities for extracts of S. africana bark and U. caffra leaves. S. cordatum leaves represented the highest affinity for protein binding with 93%. All the extracts were non-mutagenic towards the three tested strains with and without S9 metabolic activation. CONCLUSION: The result obtained in this study goes a long way in validating the ethnobotanical usage of these medicinal plants in the treatment of cough and fever by the Venda people. However, more evidence obtainable from other assays not performed here are urgently required to confirm these results.


Assuntos
Anti-Infecciosos/farmacologia , Magnoliopsida/química , Fenóis/farmacologia , Fitoterapia , Extratos Vegetais/farmacologia , Polifenóis/farmacologia , Proteínas/metabolismo , Anti-Infecciosos/efeitos adversos , Anti-Infecciosos/uso terapêutico , Bactérias/efeitos dos fármacos , Candida albicans/efeitos dos fármacos , Tosse/tratamento farmacológico , Euphorbiaceae/química , Febre/tratamento farmacológico , Flavonoides/efeitos adversos , Flavonoides/farmacologia , Flavonoides/uso terapêutico , Humanos , Medicinas Tradicionais Africanas , Testes de Sensibilidade Microbiana , Fenóis/efeitos adversos , Fenóis/uso terapêutico , Casca de Planta , Extratos Vegetais/efeitos adversos , Extratos Vegetais/uso terapêutico , Folhas de Planta , Plantas Medicinais/química , Polifenóis/efeitos adversos , Polifenóis/uso terapêutico , Ligação Proteica/efeitos dos fármacos , Proteínas/química , Rhus/química , África do Sul , Syzygium/química , Taninos/efeitos adversos , Taninos/farmacologia , Taninos/uso terapêutico , Uvaria/química
17.
Clin Pediatr (Phila) ; 51(2): 181-5, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21917545

RESUMO

The problem of tooth discoloration is emerging in our society because of the poor oral hygiene, physical agents, environmental chemicals, mouth rinses, some dental procedures, general systemic conditions, and drugs. Other common causes of tooth discoloration include excessive use of tea, coffee, tobacco smoking and chewing, chewing of betel morsel (piper betel, paan), and so on. Drug-induced tooth discoloration can be prevented by avoiding prescriptions of well-known offender drugs known to cause tooth discoloration during pregnancy and in young children. This review describes some important groups of drugs that cause tooth discoloration.


Assuntos
Descoloração de Dente/induzido quimicamente , Anti-Infecciosos/efeitos adversos , Cariostáticos/efeitos adversos , Criança , Feminino , Fluoretos/efeitos adversos , Humanos , Lactente , Compostos de Ferro/efeitos adversos , Antissépticos Bucais/efeitos adversos , Gravidez , Efeitos Tardios da Exposição Pré-Natal/induzido quimicamente , Taninos/efeitos adversos
18.
Int J Food Sci Nutr ; 62(8): 826-34, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21619459

RESUMO

Inherent phytic acid and tannins interfere with bioavailability of iron and zinc from plant-based foods. Food acidulants, ß-carotene-rich vegetables and Allium spices are understood to promote mineral bioaccessibility (an estimate of bioavailability using in vitro method) from food grains. In this study, we have verified whether these promoters would counter negative effects of phytate and tannin on bioaccessibility of iron and zinc from grains. Combinations of promoters - amchur, carrot and onion with phytic acid and tannin exogenously added individually were examined for their influence on iron and zinc bioaccessibility from the food grain. Effect of these promoters was generally dominant in the presence of phytic acid or tannic acid. The negative effect of the inhibitor was not only annulled, but also the positive influence of the promoter was fully retained. This information helps to evolve diet-based strategy to maximize mineral bioavailability and prevent deficiency situations prevalent in population dependent on plant foods.


Assuntos
Grão Comestível/metabolismo , Aditivos Alimentares/farmacologia , Ferro/metabolismo , Ácido Fítico/efeitos adversos , Extratos Vegetais/farmacologia , Taninos/efeitos adversos , Zinco/metabolismo , Disponibilidade Biológica , Daucus carota , Deficiências Nutricionais/metabolismo , Deficiências Nutricionais/prevenção & controle , Dieta , Mangifera , Cebolas , Extratos Vegetais/efeitos adversos , Especiarias , Oligoelementos/metabolismo , beta Caroteno/farmacologia
19.
Arq. bras. med. vet. zootec ; 62(4): 837-844, Aug. 2010. tab
Artigo em Inglês | LILACS | ID: lil-562050

RESUMO

In order to study the effects of tannins at histomorphological level, mice were either fed with three structurally different types of tannins (tannic acid, chestnut, and quebracho) or treated with isoproterenol, during 10 days. Acini of parotid and submandibular glands increased significantly, being the increase higher for parotid compared to submandibular glands, and higher in the quebracho compared with the other tannin groups. Sublingual acinar size also increased after tannin consumption, by opposition to isoproterenol-treated animals. The results present evidences that the effects produced by tannins are dependent on their structure.


Estudaram-se as alterações morfológicas das glândulas salivares, induzidas por taninos, em camundongos. Os animais foram distribuídos em grupos e tratados com três diferentes tipos estruturais de taninos (ácido tânico, chestnut e quebracho - adicionados à ração) ou isoproterenol via intraperitoneal, durante 10 dias. Os ácinos das glândulas parótida e submandibulares aumentaram significativamente de tamanho, sendo o incremento maior para a parótida que para as submandibulares, e maior com o quebracho comparado com o provocado pelos outros taninos. Os ácinos das glândulas sublinguais também aumentaram após o consumo de taninos em relação aos ácinos dos animais tratados com isoproterenol. Os resultados apresentam evidências de que os efeitos produzidos pelos taninos dependem de sua estrutura.


Assuntos
Animais , Camundongos , Glândulas Salivares/anatomia & histologia , Taninos/efeitos adversos , Isoproterenol , Camundongos
20.
Mar Drugs ; 8(4): 1080-93, 2010 Mar 31.
Artigo em Inglês | MEDLINE | ID: mdl-20479968

RESUMO

Hypertension or high blood pressure is one of the major independent risk factors for cardiovascular diseases. Angiotensin-I-converting enzyme (EC 3.4.15.1; ACE) plays an important physiological role in regulation of blood pressure by converting angiotensin I to angiotensin II, a potent vasoconstrictor. Therefore, the inhibition of ACE activity is a major target in the prevention of hypertension. Recently, the search for natural ACE inhibitors as alternatives to synthetic drugs is of great interest to prevent several side effects and a number of novel compounds such as bioactive peptides, chitooligosaccharide derivatives (COS) and phlorotannins have been derived from marine organisms as potential ACE inhibitors. These inhibitory derivatives can be developed as nutraceuticals and pharmaceuticals with potential to prevent hypertension. Hence, the aim of this review is to discuss the marine-derived ACE inhibitors and their future prospects as novel therapeutic drug candidates for treat hypertension.


Assuntos
Inibidores da Enzima Conversora de Angiotensina/farmacologia , Produtos Biológicos/farmacologia , Desenho de Fármacos , Inibidores da Enzima Conversora de Angiotensina/efeitos adversos , Inibidores da Enzima Conversora de Angiotensina/isolamento & purificação , Animais , Produtos Biológicos/efeitos adversos , Produtos Biológicos/isolamento & purificação , Indústria Farmacêutica/métodos , Humanos , Hipertensão/tratamento farmacológico , Oligossacarídeos/efeitos adversos , Oligossacarídeos/isolamento & purificação , Oligossacarídeos/farmacologia , Peptídeos/efeitos adversos , Peptídeos/isolamento & purificação , Peptídeos/farmacologia , Taninos/efeitos adversos , Taninos/isolamento & purificação , Taninos/farmacologia
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