Influence of treatment with gum acacia on renal vascular responses in a rat model of chronic kidney disease
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Al Suleimani, Y. M.
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Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, OmanSultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
Al Suleimani, Y. M.
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Al Za'abi, M.
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Ramkumar, A.
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Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, OmanSultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
Ramkumar, A.
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Al Mahruqi, A. S.
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Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, OmanSultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
Al Mahruqi, A. S.
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Tageldin, M. H.
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Sultan Qaboos Univ, Coll Agr & Marine Sci, Dept Anim & Vet Sci, Muscat, OmanSultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
Tageldin, M. H.
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Nemmar, A.
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United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Physiol, Al Ain, U Arab EmiratesSultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
Nemmar, A.
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Ali, B. H.
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Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, OmanSultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
Ali, B. H.
[1
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机构:
[1] Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Pharmacol, Muscat, Oman
[2] Sultan Qaboos Univ, Coll Agr & Marine Sci, Dept Anim & Vet Sci, Muscat, Oman
[3] United Arab Emirates Univ, Coll Med & Hlth Sci, Dept Physiol, Al Ain, U Arab Emirates
OBJECTIVE: This study was conducted in order to investigate the effects of adenine-induced chronic kidney disease (CKD) on renal blood flow and biochemical changes in rats, and to assess the effect of treatment with gum acacia (GA) thereon. MATERIALS AND METHODS: CKD was induced by feeding rats with adenine (0.25% w/w, five weeks). Concomitantly, some of these rats were also given gum acacia (GA) (15% w/v in the drinking water). Before animals were sacrificed, changes in renal blood flow (RBF) were monitored in anaesthetized rat preparations. Several biochemical and histological renal function tests were also conducted. RESULTS: Adenine-induced CKD significantly impaired the vasopressor actions of acetylcholine, sodium nitroprusside and phenylephrine and concomitant treatment with GA abated these responses. Additionally, plasma concentrations of urea, creatinine, uric acid, indoxyl sulfate, nitrite and nitrate and urinary excretion of protein were all significantly increased by adenine. GA significantly mitigated the severity of adenine - induced changes. CONCLUSIONS: Adenine-induced CKD in rats significantly impaired renal vascular responses to acetylcholine, sodium nitroprusside and phenylephrine and this was mitigated by treatment with GA. This provides another experimental evidence for the usefulness of GA in the amelioration of CKD.