Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters

Database
Publication year range
1.
Zhongguo Zhong Yao Za Zhi ; 40(15): 3059-62, 2015 Aug.
Article in Chinese | MEDLINE | ID: mdl-26677711

ABSTRACT

To investigate the urination-reducing effect and mechanism of Zhuangyao Jianshen Wan (ZYJCW). In this study, SI rats were subcutaneously injected with 150 mg · kg(-1) dose of D-galactose to prepare the sub-acute aging model and randomly divided into the model group, the Suoquan Wan group (1.17 g · kg(-1) · d(-1)), and ZYJCW high, medium and low dose groups (2.39, 1.20, 0.60 g · kg(-1) · d(-1)) , with normal rats in the blank group. They were continuously administered with drugs for eight weeks. The metabolic cage method was adopted to measure the 24 h urine volume and 5 h water load urine volume in rats. The automatic biochemistry analyzer was adopted to detect urine concentrations of Na+, Cl-, K+. The ELISA method was used to determine serum aldosterone (ALD) and antidiuretic hormone (ADH). The changes in P2X1 and P2X3 mRNA expressions in bladder tissues of rats were detected by RT-PCR. According to the results, both ZYJCW high and medium dose groups showed significant down-regulations in 24 h urine volume and 5 h water load urine volume in (P <0.05, P <0.01), declines in Na+ and Cl- concentrations in urine (P <0.01), notable rises in plasma ALD and ADH contents (P <0.05, P <0.01) and remarkable down-regulations in the P2X1 and P2X3 mRNA expressions in bladder tissues (P <0.01). The ZYJCW low dose group revealed obvious reductions in Na+ and Cl- concentrations in urine (P <0.01). The results indicated that ZYJCW may show the urination-reducing effect by down-regulating the P2X1 and P2X3 mRNA expressions in bladder tissues of rats with diuresis caused by kidney deficiency.


Subject(s)
Aging/physiology , Diuresis/drug effects , Drugs, Chinese Herbal/pharmacology , Kidney Diseases/drug therapy , RNA, Messenger/analysis , Receptors, Purinergic P2X1/genetics , Receptors, Purinergic P2X3/genetics , Animals , Female , Gene Expression Regulation , Kidney Diseases/metabolism , Rats , Rats, Sprague-Dawley , Urinary Bladder/metabolism
2.
Chem Biol Interact ; 222: 27-36, 2014 Oct 05.
Article in English | MEDLINE | ID: mdl-25168850

ABSTRACT

Pogostemonis Herba is an important Chinese medicine widely used in the treatment of gastrointestinal dysfunction. Patchouli alcohol (PA), a tricyclic sesquiterpene, is the major active constituent of Pogostemonis Herba. This study aimed to investigate the possible anti-ulcerogenic potential of PA and the underlying mechanism against ethanol, indomethacin and water immersion restraint-induced gastric ulcers in rats. Gross and histological gastric lesions, biochemical and immunological parameters were taken into consideration. The gastric mucus content and the antisecretory activity were analyzed through pylorus ligature model in rats. Results indicated that oral administration with PA significantly reduced the ulcer areas induced by ethanol, indomethacin and water immersion restraint. PA pretreatment significantly promoted gastric prostaglandin E2 (PGE2) and non-protein sulfhydryl group (NP-SH) levels, upregulated the cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2) mRNA expression, and considerably boosted the gastric blood flow (GBF) and gastric mucus production in comparison with vehicle. In addition, PA modulated the levels of interleukin-6 (IL-6), interleukin-10 (IL-10) and tumor necrosis factor-α (TNF-α). The levels of glutathione (GSH), catalase (CAT) and malonaldehyde (MDA) were also restored by PA. However, the gastric secretion parameters (pH, volume of gastric juice and pepsin) did not show any significant alteration. These findings suggest that PA exhibited significant gastroprotective effects against gastric ulceration. The underlying mechanisms might involve the stimulation of COX-mediated PGE2, improvement of antioxidant and anti-inflammatory status, preservation of GBF and NP-SH, as well as boost of gastric mucus production.


Subject(s)
Anti-Ulcer Agents/pharmacology , Sesquiterpenes/pharmacology , Stomach Ulcer/prevention & control , Animals , Catalase/metabolism , Cytokines/blood , Dinoprostone/metabolism , Drugs, Chinese Herbal/pharmacology , Ethanol/toxicity , Gastric Mucosa/drug effects , Gastric Mucosa/pathology , Gastric Mucosa/physiopathology , Glutathione/metabolism , Indomethacin/toxicity , Male , Malondialdehyde/metabolism , Mucus/metabolism , Prostaglandin-Endoperoxide Synthases/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Rats , Rats, Sprague-Dawley , Stomach Ulcer/etiology , Stomach Ulcer/pathology , Stress, Physiological , Sulfhydryl Compounds/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL