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4.
J Coll Physicians Surg Pak ; 27(2): 92-96, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-28292386

RESUMO

OBJECTIVE: To determine the nephrotoxic effects of arsenic kushta (Kushta Sam-ul-Far) in Wistar rats. STUDY DESIGN: Experimental study. PLACE AND DURATION OF STUDY: Department of Morbid Anatomy and Histopathology, University of Health Sciences, Lahore from May to August 2014. METHODOLOGY: This experimental study was conducted on 48 healthy Wistar rats, each weighing 200 - 250 grams. The rats were randomly divided into 4 experimental groups each containing 12 rats. Group I was taken as control given flour pellets. Group II was given single dose (180 mg/kg) of arsenic kushta for 2 weeks. Group III received 150 mg/kg of arsenic kushta for 12 weeks; whereas, group IV was also given 150 mg/kg of arsenic kushta for 12 weeks along with 75 mg of BSA (bovine serum albumin). Histopathological changes in glomeruli, tubules and interstitium were noted in the kidney. RESULTS: Mesangial proliferation, thickening of basement membrane, necrosis, and interstitial edema were mainly observed in all the above groups except group I which served as control. These changes were seen in greater severity in high dose groups and the group given BSA injection along with kushta (group III, IV). CONCLUSION: Herbo-mineral preparations of arsenic kushta are nephrotoxic in rats and may have similar toxic effects in human beings.


Assuntos
Intoxicação por Arsênico/complicações , Glomérulos Renais/patologia , Síndrome Nefrótica/patologia , Esclerose/patologia , Animais , Arsênio/toxicidade , Intoxicação por Arsênico/patologia , Modelos Animais de Doenças , Glomérulos Renais/efeitos dos fármacos , Síndrome Nefrótica/induzido quimicamente , Fotomicrografia , Plantas Medicinais/toxicidade , Ratos , Ratos Wistar , Esclerose/induzido quimicamente
6.
Nihon Shokakibyo Gakkai Zasshi ; 111(1): 61-8, 2014 Jan.
Artigo em Japonês | MEDLINE | ID: mdl-24390259

RESUMO

BACKGROUND: Mesenteric phlebosclerosis (MP) is a relatively rare disease of the colon. An association between MP and Chinese herbal medicine intake has recently been recognized. SUBJECTS AND METHODS: In the present study, we investigated the association between MP and Chinese herbal medicine intake in 42 patients, including those reported in the literature as well as those treated by us. RESULTS: Approximately 90% patients treated by us reported a history of Chinese herbal medicine intake, particularly kamishoyosan, orengedokuto, and sanshishi (gardeniae fructus), the lattermost being consumed by the majority of patients as a crude herbal medicine. DISCUSSION: Several MP patients report a history of Chinese herbal medicine intake. Furthermore, symptoms are exacerbated in MP patients who continue to consume the medicine after onset. Interestingly, MP was reported to develop in a married couple who had consumed the same Chinese herbal medicine for a prolonged period. These findings suggest that the intake of Chinese herbal medicine, particularly sanshishi, is strongly associated with MP development.


Assuntos
Medicamentos de Ervas Chinesas/efeitos adversos , Veias Mesentéricas , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Esclerose/induzido quimicamente
7.
Nihon Shokakibyo Gakkai Zasshi ; 109(9): 1567-74, 2012 Sep.
Artigo em Japonês | MEDLINE | ID: mdl-22976226

RESUMO

A 59-year-old woman had been admitted to our hospital every two months for over a past year because of severe right abdominal pain. Colonoscopy revealed dark blue mucosa extending from the cecum to the transverse colon, and abdominal computed tomography showed wall thickening and linear calcification along the wall from the cecum to the transverse colon. Based on these findings, the patient was given a diagnosis of idiopathic mesenteric phlebosclerosis. Subsequently, we found that she had been a long-term user of a Chinese herbal product containing Gardeniae fructus for allergic rhinitis. After discontinuing the product, the patient has been free of abdominal pain for a year.


Assuntos
Gardenia/efeitos adversos , Medicina Tradicional Chinesa/efeitos adversos , Veias Mesentéricas/patologia , Esclerose/induzido quimicamente , Feminino , Humanos , Pessoa de Meia-Idade , Esclerose/patologia
8.
Aliment Pharmacol Ther ; 36(6): 575-86, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22817400

RESUMO

BACKGROUND: Idiopathic mesenteric phlebosclerosis (IMP) is a rare disease, characterised by thickening of the wall of the right hemicolon with calcification of mesenteric veins. However, the aetiology remains unknown. AIM: To investigate the possible association of herbal medicines with IMP. METHOD: The clinical data of four of our own patients were collected. Furthermore, we searched for previous reports about similar patients with detailed descriptions of herbal prescriptions that they had taken. We compared herbal ingredients to identify the toxic agent as a possible aetiological factor. RESULTS: Clinical data on a total of 25 patients were summarised. Mean age was 61.8 years and there was female predominance (6 men and 19 women). The used Kampo prescription, the number of cases, and the mean duration of use were as follows: kamisyoyosan in 12 cases for 12.8 years, inshin-iseihaito in 5 cases for 13.4 years, orengedokuto in 4 cases for 14.3 years, inchinkoto in 1 case for 20 years, kamikihitou in 1 case for 19 years, seijobofuto in 1 case for 10 years and gorinsan in 1 case for an unknown duration. Only one ingredient, sansisi, was common to the herbal medicines of all 25 patients. This crude drug called geniposide in English is a major constituent of the Gardenia fruits. CONCLUSION: The long-term use of geniposide in herbal medicines appears to be associated with mesenteric phlebosclerosis.


Assuntos
Medicamentos de Ervas Chinesas/efeitos adversos , Iridoides/efeitos adversos , Oclusão Vascular Mesentérica/induzido quimicamente , Veias Mesentéricas/patologia , Plantas Medicinais/efeitos adversos , Idoso , Biópsia , Feminino , Humanos , Mucosa Intestinal/patologia , Masculino , Oclusão Vascular Mesentérica/diagnóstico por imagem , Oclusão Vascular Mesentérica/patologia , Pessoa de Meia-Idade , Esclerose/induzido quimicamente , Fatores de Tempo , Tomografia Computadorizada por Raios X
9.
Amino Acids ; 38(4): 1021-30, 2010 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-19533301

RESUMO

Glutamine is the most important donor of NH(3) in kidney playing an important role in acid-base buffering system. Besides this effect, glutamine presents many other relevant functions in the whole body, such as a precursor of arginine in adult and neonates. In addition to these effects, some studies have shown that glutamine can potentiate renal disease. In the present study, the effect of short-term treatment (15 days) with glutamine on control and diabetic rats was investigated. Using biochemical, histological and molecular biology analysis from control and diabetic rats we verified that glutamine supplementation increase in pro-inflammatory interleukins (IL)-1beta and IL-6 content in renal cortex and induce alteration in glomerular characteristics. This study showed that short-term treatment with glutamine in association with increased glucose levels could cause important alterations in glomerular morphology that may result in fast progression of kidney failure.


Assuntos
Diabetes Mellitus Experimental/patologia , Nefropatias Diabéticas/patologia , Glutamina/toxicidade , Rim/patologia , Animais , Glicemia/análise , Contraindicações , Diabetes Mellitus Experimental/metabolismo , Nefropatias Diabéticas/induzido quimicamente , Nefropatias Diabéticas/metabolismo , Suplementos Nutricionais/toxicidade , Regulação da Expressão Gênica , Glomerulonefrite/induzido quimicamente , Glomerulonefrite/patologia , Glutamina/sangue , Glicosúria/induzido quimicamente , Interleucina-1beta/genética , Interleucina-1beta/metabolismo , Interleucina-6/genética , Interleucina-6/metabolismo , Rim/metabolismo , Córtex Renal/metabolismo , Córtex Renal/patologia , Glomérulos Renais/patologia , Masculino , Nitrogênio/metabolismo , Ratos , Ratos Wistar , Esclerose/induzido quimicamente , Esclerose/patologia , Índice de Gravidade de Doença
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