Animals
Male albino Wistar rats (200 ± 20 g) were obtained from the animal house of the School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Iran. They were housed under standard the laboratory conditions and had access to standard rat chow and water. Rats were allowed to acclimatize to laboratory condition for 1 week before the experiments. All the experimental procedures were according the standard ethical guidelines for laboratory animal use and care as described by the Animal Ethical Committee of Isfahan University of Medical Sciences.
Materials
Protocatechuic acid (3, 4-dihydroxybenzoic acid) was obtained from Serva Feinbiochemica (Heidelberg, Germany). Dexamethasone and vitamin C (ascorbic acid) were purchased from Darou Pakhsh Pharmaceutical Co. (Tehran, Iran) and captopril was purchased from Tehran Darou Pharmaceutical Co. (Tehran, Iran). The measurement of plasma lipid hydroperoxides and ferric reducing antioxidant power (FRAP) were done using standard assay kits (Hakiman Shargh Research Co., Isfahan, Iran).
Experimental protocol
In this prevention study, oral administration of drugs using an intragastric tube was started from 4 days before induction of hypertension by Dex and continued during the test period. Rats were randomly divided into seven groups as follows: (i) group 1 as the saline control group received daily injection of saline (1 mL/kg, s.c.) for 14 days (Days 4-18); (ii) group 2 as the Dex control group received daily injection of Dex (30 µg/kg, s.c.) for 14 days (Days 4-18) (17); (iii) group 3 as the antihypertensive positive control group received daily oral administration of captopril (40 mg/kg) (Days 0-18); (iv) group 4 as the antioxidant positive control group received daily oral administration of vitamin C (750 mg/kg) (Days 0-18); groups 5 to 7 received daily oral administration of different doses of PCA (50, 100 and 200 mg/kg) (Days 0-18).
The saline and Dex control rats were also received PCA vehicle (1% carboxymethyl cellulose in saline) orally. Six rats were used in each group. Rats were weighed on alternate days between 10 AM and 12 noon. At the end of the experiment, all groups of animal were sacrificed under ether anesthesia. The thymus gland was removed. The blood samples were collected into heparinized tubes and plasma was separated for further experiments.
Measurement of systolic blood pressure
The systolic blood pressure (SBP) was recorded at the first day and the last day of the experiment (days 1 and 18), between 10 AM and 12 noon, by non-invasive tail-cuff method (AD Instrument PowerLab Data Acquisition System, Australia). Rats were trained with instrument for one week before initiation of the experiment and were conscious during the measurement. The animals were placed in a heated restrainer at 37 ± 1 ºC for 10 minutes. At least 3 blood pressures were measured for each rat and the average of them was reported as the SBP.
Measurement of thymus weight
The thymus weight, as a marker of glucocorticoid activity was measured and reported as mg/100g of body weight (
18).
Measurement of plasma hydrogen peroxide concentration
A colorimetric assay kit based on the ferrous ion oxidation by xylenol orange reagent in aqueous medium with sorbitol (FOX1) was used for the measurement of plasma hydrogen peroxide (H
2O
2) concentration (
19). In brief, FOX1 reagent prepared according to the manufacturer’s protocol was mixed with the plasma samples and incubated for 30 min in 37 ºC. The absorbance of solutions was measured at 540 nm using a microplate reader/spectrophotometer (Bio-Tek, Power Wave XS). The H
2O
2 concentration of plasma samples was calculated using a standard curve obtained from different concentrations of H
2O
2.
Measurement of plasma ferric reducing antioxidant power
A colorimetric assay kit was used for measurement of the total antioxidant capacity of plasma samples by ferric reducing antioxidant power (FRAP) assessment (
20). FRAP was evaluated based on the reduction of ferric-tripyridyltriazine complex to ferrous form. In brief, the FRAP reagent according to the manufacturer’s protocol was added to the plasma samples and incubated for 40 min in 40 °C. The absorbance of colored solutions was measured at 570 nm using a microplate reader/spectrophotometer. The FRAP value of samples were calculated against the standard curve of FeSO4x7H2O concentrations and expressed as micromole of Fe II equivalents per liter.
Statistical analysis
Statistical analysis was performed by one-way analysis of variance (ANOVA) followed by Tukey post-hoc test using SPSS software version 16.0. The data were shown as the mean ±SEM. P value < 0.05 was considered to be statistically significant.