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3.
J Coll Physicians Surg Pak ; 27(2): 92-96, 2017 02.
Artículo en Inglés | MEDLINE | ID: mdl-28292386

RESUMEN

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.


Asunto(s)
Intoxicación por Arsénico/complicaciones , Glomérulos Renales/patología , Síndrome Nefrótico/patología , Esclerosis/patología , Animales , Arsénico/toxicidad , Intoxicación por Arsénico/patología , Modelos Animales de Enfermedad , Glomérulos Renales/efectos de los fármacos , Síndrome Nefrótico/inducido químicamente , Fotomicrografía , Plantas Medicinales/toxicidad , Ratas , Ratas Wistar , Esclerosis/inducido químicamente
5.
Nihon Shokakibyo Gakkai Zasshi ; 111(1): 61-8, 2014 Jan.
Artículo en Japonés | MEDLINE | ID: mdl-24390259

RESUMEN

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.


Asunto(s)
Medicamentos Herbarios Chinos/efectos adversos , Venas Mesentéricas , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Humanos , Masculino , Persona de Mediana Edad , Esclerosis/inducido químicamente
6.
Nihon Shokakibyo Gakkai Zasshi ; 109(9): 1567-74, 2012 Sep.
Artículo en Japonés | MEDLINE | ID: mdl-22976226

RESUMEN

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.


Asunto(s)
Gardenia/efectos adversos , Medicina Tradicional China/efectos adversos , Venas Mesentéricas/patología , Esclerosis/inducido químicamente , Femenino , Humanos , Persona de Mediana Edad , Esclerosis/patología
7.
Aliment Pharmacol Ther ; 36(6): 575-86, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22817400

RESUMEN

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.


Asunto(s)
Medicamentos Herbarios Chinos/efectos adversos , Iridoides/efectos adversos , Oclusión Vascular Mesentérica/inducido químicamente , Venas Mesentéricas/patología , Plantas Medicinales/efectos adversos , Anciano , Biopsia , Femenino , Humanos , Mucosa Intestinal/patología , Masculino , Oclusión Vascular Mesentérica/diagnóstico por imagen , Oclusión Vascular Mesentérica/patología , Persona de Mediana Edad , Esclerosis/inducido químicamente , Factores de Tiempo , Tomografía Computarizada por Rayos X
8.
Amino Acids ; 38(4): 1021-30, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-19533301

RESUMEN

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.


Asunto(s)
Diabetes Mellitus Experimental/patología , Nefropatías Diabéticas/patología , Glutamina/toxicidad , Riñón/patología , Animales , Glucemia/análisis , Contraindicaciones , Diabetes Mellitus Experimental/metabolismo , Nefropatías Diabéticas/inducido químicamente , Nefropatías Diabéticas/metabolismo , Suplementos Dietéticos/toxicidad , Regulación de la Expresión Génica , Glomerulonefritis/inducido químicamente , Glomerulonefritis/patología , Glutamina/sangre , Glucosuria/inducido químicamente , Interleucina-1beta/genética , Interleucina-1beta/metabolismo , Interleucina-6/genética , Interleucina-6/metabolismo , Riñón/metabolismo , Corteza Renal/metabolismo , Corteza Renal/patología , Glomérulos Renales/patología , Masculino , Nitrógeno/metabolismo , Ratas , Ratas Wistar , Esclerosis/inducido químicamente , Esclerosis/patología , Índice de Severidad de la Enfermedad
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