Effects of immune-activated platelets and LDL on expression and activity of COX-2 and PPAR-α in HUVECs

AIM: To observe the effect of immune-activated platelets and low-density lipoprotein cholesterol (LDL) on the expression and activity of cyclooxygenase-2 (COX-2) and peroxisome proliferator activated receptor α (PPAR-α) in human umbilical vein endothelial cells (HUVECs) treated with activated platelets and LDL. METHODS: The platelets were activated by ADP. The co-culture system of HUVECs with immune activated platelets and/or LDL were established. The activity of COX-2 and expression of PPAR-α at mRNA and protein levels in HUVECs were detected by RT-PCR and Western blotting. The concentration of PGE2 was measured by ELISA for representing the COX-2 activity. The PPAR-α activity was determined by a nuclear factor assay kit. RESULTS: The COX-2 activity and mRNA expression of PPAR-α, the protein levels of COX-2 and PPAR-α and PGE2 concentration in activated platelets group were significant higher than those in un-activated platelets group (all P<0.01). No difference of PPAR-α binding activity was observed between two groups. LDL didnt affect the COX-2 activity and PPAR-α expression, but significantly promoted the stimulating effect of immune-activated platelets. CONCLUSION: Immune-activated platelets significantly promote COX-2 activity and PPAR-α expression in HUVECs, but dont change the PPAR-α binding activity. LDL at general concentration does not affect the expression and activity of COX-2 and PPAR-α, but promote the effect of activated platelets on HUVECs.     

The effect of ε-aminocaproic acid on self-incompatibility and incongruity in Phaseolus

Summary

The effects of ε-aminocaproic acid (EACA) on self-incompatibility was tested in a Phaseolus coccineus line which failed to form pods in controlled pollinations. Scanning electron microscope (SEM) and fluorescence miscroscopy confirmed problems in pollen-germination and pollen-tube growth but EACA-treated self- pollinations resulted in fairly normal pollen germination and pollen tube growth. In a few cases, pollen tubes were seen entering the embryo sac and occasionally pods were formed. Incongruity barriers also exist in crosses of P. coccineus × P. vulgaris, P. acutifolius × P. coccineus and their reciprocals. Effects of EACA on flower abscission, pod development and pod abscission were studied. Increased pod formation was observed in EACA treated materials, except in P. acutifolius × P. coccineus and P. coccineus × P. vulgaris cv. Jacobs Cattle. EACA seems to act at the stigmatic and stylar levels, thereby enhancing pollen germination and pollen tube growth and delaying flower abscission. The net result is fertilization and delayed senescence which permit the pod to grow for a longer period of time.     

Effect of PPARδ activation on expression of MMP-9 and fibronectin in infarcted myocardium

AIM:To investigate the effect of peroxisome proliferator-activated receptor δ (PPARδ) activation with dietary GW610742X on the expression of matrix metalloproteinase-9 (MMP-9) and fibronectin (FN) in infarcted and remodeling myocardium. METHODS: Wistar rats were divided into 4 groups: control group, sham group, myocardial infarction (MI) group and MI+GW610742X (GW) group. The left coronary artery was ligated to establish the MI model. PPARδ activator GW610742X (100 mg·kg^-1·d^-1) was given to the rats in GW group. At the 3rd month of the procedure, the expression of PPARδ, MMP-9 and FN at mRNA and protein levels in the left ventricular free wall(LVFW) of the heart from each group was identified and the distribution of FN was detected by immunofluorescence. RESULTS: After 3 months following the procedure, obvious necrosis and fibrosis in LVFW were observed in MI group. The expression of PPARδ in MI group was higher than that in control, sham and GW groups (P<0.01), and PPARδ expression in GW group was lower than that in control and sham group (P<0.05). In MI and GW groups, the expression of MMP-9 was higher while the expression of FN was lower than those in control and sham group (P<0.05 or P<0.01). In GW group, the expression of MMP-9 was lower (P<0.05) while the expression of FN was higher (P<0.01) than those in MI group. Meanwhile, the expression of MMP-9 and FN in sham group was similar to those in control group (P>0.05). CONCLUSION: MMP-9 is upregulated and FN is downregulated in infarcted myocardium during the remodeling process. Activation of PPARδ inhibits the upregulation of MMP-9 and degradation of FN, thus ameliorating the myocardial remodeling.     

Effect of pioglitazone on glucose metabolism and PPAR-γ expression in lipid-infused rats

AIM: To investigate the effect of pioglitazone (Pio) on glucose metabolism and peroxisome proliferators-activated receptor (PPAR)-γ expression in free fatty acid (FFA) -induced insulin resistance in rats. METHODS: A hyperinsulinaemic-euglycaemic clamp and ［3-3H］-glucose tracing technique were used in awake rats. Glucose metabolism in vivo and PPAR-γ in adipose tissue expression were assessed with elevation FFA by lipid infusion over 4 h in rats pretreated with or without Pio.RESULTS: During steady-state of clamp, there was a significant increase in plasma FFA in two lipid-infused groups, compared to control rats (P<0.01). The glucose infusion rates (GIR) in Pio-treated rats (P/L group), compared with controls, were significantly reduced ［(20.6±0.4) mg·kg^-1·min^-1 vs (33.6±0.6)mg·kg^-1· min^-1, P<0.01］, whereas the GIR was lower in the lipid group (L group) than that in the P/L group［(12.6±0.8) mg·kg^-1·min^-1 vs (20.6±0.4) mg·kg^-1·min^-1, P<0.01］. The hepatic glucose production (HGP) was significantly suppressed (85%) ［(18.3±2.1)mg· kg^-1·min^-1 (basal) vs (2.7±2.4)mg· kg^-1·min^-1, and (17.5±2.6) mg· kg^-1·min^-1 vs (2.6±1.0)mg· kg^-1·min^-1］, all P<0.01 during clamp in control and P/L groups. The suppressive effect of insulin on HGP was significantly blunted in L group［(17.3±2.1)mg· kg^-1·min^-1 vs (15.8±1.5)mg· kg^-1·min^-1］. The rate of glucose disappearance (GRd) was significantly reduced in two lipid-infused rats compared with controls［(26.6±1.6)mg· kg^-1·min^-1 and (23.2±0.9)mg· kg^-1·min^-1 vs (37.7±2.6)mg·kg^-1·min^-1,P<0.01］. The PPAR-γ expression of adipose tissue in P/L group was significantly upregulated. CONCLUSION: Lipid-infusion induces an acute insulin-resistance in vivo. Pio treatment upregulates the PPAR-γ of adipose tissue and suppresses HGP. Pio can protect partly against lipid-induced insulin resistance.     

Landscape and local effects on occupancy and densities of an endangered wood-warbler in an urbanizing landscape

Context

Golden-cheeked warblers (Setophaga chrysoparia), an endangered wood-warbler, breed exclusively in woodlands co-dominated by Ashe juniper (Juniperus ashei) in central Texas. Their breeding range is becoming increasingly urbanized and habitat loss and fragmentation are a main threat to the species’ viability.

Objectives

We investigated the effects of remotely sensed local habitat and landscape attributes on point occupancy and density of warblers in an urban preserve and produced a spatially explicit density map for the preserve using model-supported relationships.

Methods

We conducted 1507 point-count surveys during spring 2011–2014 across Balcones Canyonlands Preserve (BCP) to evaluate warbler habitat associations and predict density of males. We used hierarchical Bayesian models to estimate multiple components of detection probability and evaluate covariate effects on detection probability, point occupancy, and density.

Results

Point occupancy was positively related to landscape forest cover and local canopy cover; mean occupancy was 0.83. Density was influenced more by local than landscape factors. Density increased with greater amounts of juniper and mixed forest and decreased with more open edge. There was a weak negative relationship between density and landscape urban land cover.

Conclusions

Landscape composition and habitat structure were important determinants of warbler occupancy and density, and the large intact patches of juniper and mixed forest on BCP (>2100 ha) supported a high density of warblers. Increasing urbanization and fragmentation in the surrounding landscape will likely result in lower breeding density due to loss of juniper and mixed forest and increasing urban land cover and edge.

     

Role of ZIPK in the regulatory effects of PKCα and PKCε on calcium sensitivity during hemorrhagic shock in rats

AIM: To observe the role of zipper-interacting protein kinase (ZIPK) in the regulatory effects of protein kinase Cα (PKCα) and protein kinase Cε (PKCε) on calcium sensitivity during hemorrhagic shock(HS) in rats. METHODS: The skinned first class arborization of superior mesenteric artery (SMA) from HS rats were adopted to observe the influence of inhibitor of ZIPK on the effects of PKCα and PKCε agonists on calcium sensitivity after shock via measuring the contraction initiated by Ca2+ with isolated organ perfusion system, hypoxic vascualr smooth muscle cells (VSMCs) were adopted to measure the protein expression and activity of ZIPK after applying PKCα and PKCε agonists following hypoxia via Western blotting. RESULTS: (1) The calcium sensitivity of SMA was decreased after 2 h shock, and increased by agonists of PKCα and PKCε. Emax of Ca2+ was increased from 47.2％to 66.5％ (P<0.01) and 66.3％ (P<0.01) of normal control respectively as compared with 2 h shock group. The increasing effects of PKCα and PKCε agonists on calcium sensitivity of SMA after 2 h shock were weakened by the inhibitor of ZIPK. The cumulative dose-response curve of Ca2+ was shifted to the right, the Emax of Ca2+ was decreased to 42.6％ and 47.5％ of normal control (P<0.01), respectively. (2) The protein expression and activity of ZIPK in VSMCs were decreased after 2 h hypoxia, and were increased by the agonists of PKCα and PKCε following 2 h hypoxia. CONCLUSION: PKCα and PKCε regulate the calcium sensitization probably through changing the protein expression and activity of ZIPK following HS in rats.     

Role of nucleolin on myocardial hypertrophy and fibrosis in type Ⅱ diabetic cardiomyopathy mice

AIM:To investigate the effect of nucleolin on diabetic cardiomyopathy in mice.METHODS:A type Ⅱ diabetic cardiomyopathy mouse model was prepared using a cardiac-specific nucleolin-overexpressing transgenic mice.The mice were divided into wild-type mouse control group,nucleolin transgenic mouse control group,wild-type mouse diabetes group and nucleolin transgenic mouse diabetes group.Wheat germ agglutinin (WGA) fluorescent dye,Masson staining and PowerLab system detection were used to further clarify the role of nucleolin on cardiac hypertrophy,fibrosis and cardiac function in type Ⅱ diabetic cardiomyopathy mice.RESULTS:Compared with wild-type mouse control group,no significant increase in blood glucose level was found,while genetical myocardial cell hypertrophy was significantly attenuated in nucleolin transgenic mouse diabetes group.The collagen fibers were also significantly reduced,and hemodynamic indexes±dp/dt_max,left ventricular end-diastolic pressure,left ventricular systolic pressure and heart rate were also improved.The above differences were statistically significant.CONCLUSION:Nucleolin may reduce the occurrence of myocardial hypertrophy and fibrosis,thus improving the cardiac function of diabetic cardiomyopathy mice.     

Effect of stage of harvesting and seed treatment on germination,seedling emergence and growth in Corchorus olitorius ‘Oniyaya’

Fruits of Corchorus olitorius L. were harvested at three different developmental stages on the basis of colour (yellow, yellow with brown patches or completely brown). Seed germination (total and rate) and seedling emergence from soil varied with the fruit colour. Steeping the seeds in water at 97°C for 5 s and seed-coat scarification using sandpaper significantly improved seed germination and seedling emergence. Stage of harvesting also affected the shoot lengths and degree of uniformity in shoot lengths of 5-week-old seedlings.     

Effects of light on flavonoid and chlorogenic acid levels in the skin of ‘Jonagold’ apples

The objective of our work was to determine how fruit position on the tree affects flavonoid and chlorogenic acid contents. Light was measured at different positions within the canopy of 10-year-old ‘Jonagold’ apple trees on M.9 rootstock raised as slender spindles. Fruit from the top of the canopy contained the highest percentage of blush and the highest levels of cyanidin 3-galactoside (anthocyanin) and quercetin 3-glycosides, followed by fruit from the outside of the canopy, and then those from the canopy interior. There were no significant differences in the levels of catechins, phloridzin and chlorogenic acid among fruit from the different canopy positions. Light level was directly correlated with the levels of cyanidin 3-galactoside and quercetin 3-glycosides and with the percentage of blush in the fruit skin. Light in the interior of the canopy was poorer in UV-A, blue, green and red but richer in far-red light than at all other positions. Consequently, the FR/R ratio was much larger at the interior of the canopy than at all other positions. Both anthocyanin and quercetin 3-glycoside concentrations were clearly related to light level, and there was a critical FR/R ratio of about 1 below which no anthocyanin and only minimal quercetin 3-glycosides were formed.     

Effects of genotype and environment on total anti-oxidant capacity and the content of sugars and acids in strawberries (Fragaria × ananassa Duch.)

Summary

Total anti-oxidant capacity (TAC) and the contents of mono- and disaccharides, and organic acids were determined in strawberry fruit from ten genotypes sampled from eight experimental sites in Norway in 2002 and 2003. The difference between genotypes was significant for all recorded traits, and it appeared possible to select for all traits in breeding programmes. On average, the Norwegian bred cultivar ‘Carmen’ had a TAC of 30.07 mmol kg^–1 fresh weight (FW), compared to 23.16 mmol kg^–1 FW in the standard cultivar ‘Korona’. TAC was negatively correlated with fruit size, rainfall and leaf surface humidity, but was positively correlated with the minimum temperature on the day prior to sampling. Mono- and di-saccharide contents were negatively correlated with both minimum and maximum temperatures, and with wind velocity. It was confirmed that the sugars:organic acids ratio was inversely related to the maximum temperature on the day before harvest, which supports anecdotal claims that strawberries grown in northern areas have, on average, better flavour.     

Effects of arsenic trioxide on activities of MMPs and expression of TIMP-1 and TGF-β1 in skin fibroblasts and polymorphonuclear neutrophils

AIM: To observe the effects of arsenic trioxide (As₂O₃) on activities of matrix metalloproteinases (MMPs), expression of tissue inhibitor of metalloproteinase-1 (TIMP-1) and transforming growth factor beta1 (TGF-β₁) in human fibroblast (hFb), and to discuss weather As₂O₃ promotes the healing of chronic skin ulcer through regulating collagen metabolism. METHODS: Zymography was used for testing activity of MMP-9 deriving from rat polymorphonuclear neutrophils (PMNs) and activities of MMP-1, MMP-2 secreted by hFb. Immunocytochemical method was used to determine the expressions of TIMP-1 and TGF-β₁. RESULTS: At the concentration of 50 mg/L, As₂O₃ elevated the activity of MMP-9 (P<0.01). At the concentration of 0.8 mg/L, As₂O₃ increased the activities of MMP-1 and MMP-2 (P<0.01, respectively). After hFb was cultured with As₂O₃ for 6 h, 12 h and 18 h, the expressions of TIMP-1 and TGF-β₁ decreased continuously (P<0.01). CONCLUSION: As₂O₃ elevates the activities of MMP-1, MMP -2 and MMP-9, also inhibits the expressions of TIMP-1 and TGF-β₁, suggesting that arsenic preparation may exert positive effect on healing chronic skin ulcer through regulating collagen metabolism.     

Effect of TNF-α and Yigu capsule drug-containing sera on osteoblasts apoptosis in coculture system

AIM: To observe the effect of TNF-α and Yigu capsule drug-containing sera on osteoblasts apoptosis in osteoblasts-osteoclasts coculture system.METHODS: (1) Twenty female Sprague-Dawley rats, 10 months old, were randomly assigned into 2 groups, NS and Yigu capsule groups, to prepare blank sera and drug-containing sera. (2) The DNA gel electrophoresis method was used to detect apoptosis of osteoblasts treated with different concentration of TNF-α in order to determine the best dosage in the co-culture system. (3) The cells were divided into four groups, TNF-α group, normal group, TNF-α + blank serum group and TNF-α + drug-containing serum group. DNA gel electrophoresis, acridine orange staining and flow cytometry were used to observe osteoblast apoptosis in these groups. RESULTS: (1) After induced by TNF-α for 72 h at a concentration of 60 μg/L, relatively typical DNA ladder appeared in TNF-α group. (2) Only two DNA brands appeared and most of cells were well-proportioned stained in TNF-α + drug-containing serum group, the rate of osteoblasts apoptosis in TNF-α + drug-containing serum group (9.60%±0.26%) was obviously lower than that in the TNF-α group (26.90%±0.06%) and TNF-α + blank serum group (18.10%±0.06%). CONCLUSION: TNF-α induces osteoblast apoptosis in the co-culture system, and Yigu capsule drug- containing serum prevents osteoblast apoptosis induced by TNF-α.     

Influence of macronutrient composition,TIBA and dark treatment on shoot formation and nitrogen content in petiole explants of Senecio × hybridus

Summary

The content of ammonium, nitrate and potassium was varied in the macronutrient solutions intended for formation of adventitious shoots from petiole expiants of Senecio × hybridus. The other components of the macronutrients were according to Murashige and Skoog (1962). The largest number of expiants which formed shoots was obtained when the nitrogen concentration in the Murashige-Skoog solution was lowered from 60 to 30 mM and the potassium concentration from 20 to 15 mM. Addition of 1.0 μM TIBA to the medium as well as the standard addition of 4.44 μM BAP and 28.5 μM IAA favoured shoot formation. Even growth in darkness for two weeks immediately after expiant excision increased shoot number. The nitrogen content in the tissue decreased as the nitrogen concentration in the medium decreased, although an increased concentration in the medium from 60 to 75 mM did not increase the nitrogen content in the tissue. When the potassium concentration was changed from 20 to 15 mM, in a medium with 30 mM nitrogen, the nitrogen concentration in the tissue increased. On the other hand, when using a medium with 60 mM nitrogen, the potassium concentration (30 and 20 mM) did not affect the nitrogen content of the tissue.     

Effect of erythromycin on transforming growth factor-β1 and γ-glutamylcysteine synthetase in lung of smoking rats

AIM: To investigate the effect of erythromycin on the level of transforming growth factor-β₁ (TGF-β₁) and γ-glutaglutamylcysteine synthetase (γ-GCS) in smoking rats,and to explore the antioxidate therapeutic role of erythromycin in chronic obstructive pulmonary disease.METHODS: Wistar rats were exposed to cigarettes smoking to establish the model.After passive smoking for 4 weeks,erythromycin intragastric intervention was administered continuously for 8 weeks.The expiratory airway resistance and lung compliance were assessed and the expression levels of TGF-β₁ and γ-GCS proteins (and the mRNA) in airway endothelial cells and alveolar macrophages were observed respectively by immunohistochemical,immunocytochemical and (in situ) hybridization.RESULTS: The expiratory airway resistance was increased and the lung compliance was degraded significantly in smoking group and erythromycin group,compared to control group.In erythromycin group,the airway resistance was lower and the lung compliance was higher than that in smoking group (P<0.05).The levels of TGF-β₁ and γ-GCS in smoking group and erythromycin group was obviously increased in airway endothelial cells and alveolar macrophages in comparison with control group (P<0.05).The levels of TGF-β₁ and γ-GCS were inhibited by erythromycin (P<0.05).TGF-β₁ was obviously positive correlated with γ-GCS in smoking group,but this was not found in erythromycin group.CONCLUSION: Erythromycin therapy improves pulmonary function and relieves emphysema change induced by smoking in rats,and decreases the expression of TGF-β₁ and γ-GCS in alveolar macrophages and airway endothelial cells,suggesting that erythromycin may play a role in the antioxidate therapeutic in COPD.     

Effect of TNF-α on production and activation of caspase-3 in primary rat renal proximal tubule cells

AIM: To investigate the production and activation of caspase-3 in primary rat renal proximal tubule cells in response to tumor necrosis factor-α(TNF-α) and the implication of nuclear factor-κB (NF-κB) in the process. METHODS: Isolated rat renal proximal tubule cells (PTCs) from male adult Sprague Dawley rats were treated with TNF-α according to the indicated time courses. A specific NF-κB inhibitor, Bay11-7082, was used alone or as a pretreatment for 1 h followed by exposure to TNF-α for 24 h. The protein levels of cleaved caspase-3, caspase-3, I-κBα, phosphorylated I-κBα, and GAPDH were detected by Western blotting using specific antibodies. RESULTS: The protein level of cleaved caspase-3 relative to caspase-3 was significantly increased in the presence of TNF-α for 6 h, 12 h, and 24 h. Protein levels of caspase-3 were significantly decreased by 12 h and returned to baseline by 24 h in the presence of TNF-α. Treatment with Bay11-7082 for 25 h alone or pretreatment with Bay11-7082 for 1 h followed by addition of TNF-α for 24 h caused a remarkable reduction in both cleaved caspase-3 and caspase-3 as compared to control and TNF-α treated groups. An increase in phosphorylated I-κBα was observed from 15 min to 60 min after treatment with TNF-α at a dose of 10 μg/L in PTCs. CONCLUSION: NF-κB is not only associated with the activation of caspase-3 but also the production of caspase-3 in primary rat renal proximal tubule cells in response to TNF-α.     

Effect of crop load,fruit position and shoot vigour on yield and quality of Annona atemoya × Annona squamosa in India

The effect of crop load, position of the fruit on the shoots and vigour of the shoots on yield and quality of Annona atemoya × A. squamosa hybrid ‘Arka Sahan’ was investigated in India over two years. The trees were hand-pollinated and thinned to 20, 40, 60, 80 or 100 fruit after fruit set. Information was collected on total and marketable yield, yield efficiency, average fruit fresh weight, peel weight, the number of seeds per 100 g of pulp, pulp content in the fruit, total soluble solids (TSS) and total titratable acidity. In other experiments, fruit were harvested from weak, medium or vigrous shoots, or from basal, middle or apical nodes. Total yield increased up to 60 or 80 fruit per tree and marketable yield increased up to 60 fruit per tree. Average fruit weight and peel weight increased as cropping increased. These results suggest that optimum productivity and quality is associated with 60 fruit per tree or 0.17 to 0.19 kg cm² trunk-cross sectional area. The quality of the fruit in different positions on the shoots or on the different types of shoots was highly variable and generally not affected by the various treatments.     

Effects of TNF-α-mediated insulin resistance on INSIG2 and SCAP expressions in vivo

AIM: To investigate the effects of TNF-α induced insulin resistance (IR) on INSIG1, INSIG2, SCAP and SREBP expressions in mice. METHODS: Male C57BL/6J mice were randomly divided into 4 groups. The mice were given an intraperitoneal injection of TNF-α (6 μg·kg-1·d-1; 3 μg·kg-1·d-1 and 1 μg·kg-1·d-1) and saline (NC group) twice daily for 7 d. The insulin sensitivity and glucose metabolism in awaken mice were evaluated by intravenous glucose tolerance test (IVGTT). The mRNA expression and protein levels of gene were measured by RT-PCR and Western blotting. RESULTS: After TNF-α treatment, fasting blood glucose (FBG), plasma insulin and free fatty acids (FFA) were significantly elevated in TNF-α (6 μg·kg-1·d-1) group compared to NC, TNF-α (1 μg·kg-1·d-1) and TNF-α (3 μg·kg-1·d-1) groups (P<0.01 and P<0.05, respectively). There was a lower glucose tolerance in TNF-α (6 μg·kg-1·d-1) group than that in other three groups during IVGTT. In TNF-α (6 μg·kg-1·d-1) group, the insulin release of glucose-stimulation was higher than that in NC and TNF-α (1 μg·kg-1·d-1) groups (P<0.01 and P<0.05). The INSIG2 mRNA expression of adipose tissues in TNF-α (6 μg·kg-1·d-1) group was significantly increased compared with NC group (P<0.01), and INSIG2 protein levels were also increased (P<0.05). In TNF-α treatment mice, SCAP mRNA level in adipose tissues was significantly up-regulated than that in the controls (P<0.05). The mRNA expressions of INSIG1 and SREBP1 in two groups were not significantly changed (P>0.05). CONCLUSION: In TNF-α induced insulin resistance, INSIG2 and SCAP may be involved in the pathways of lipid metabolism.     

Early treatment with aminoguanidine on level of plasma and renal AngⅡ in diabetic rats

AIM: To investigate the effect of aminoguanidine (AG) on plasma and renal levels of angiogenesis Ⅱ (AngⅡ), and to identify the relationship of AGEs with AngⅡ in STZ-induced diabetic rats. METHODS: Wistar rats were randomly assigned to three groups. Diabetes was induced, rats were then received AG in treatment group. At the end of 12th week, urine albumin excretion rate (UAER) and calculate creatinine clearance (Ccr) were detected. Periodic acid-Schiff reagent was used to evaluate renal pathology. Plasma and renal AngⅡ were analyzed by radioimmunoassay and immunohistochemistry, respectively. RESULTS: AG treatment significantly prevented the increase in UAER (P<0.01), renal pathology (P<0.01), and level of renal AngⅡ (P<0.01). However, plasma concentration of AngⅡ was higher than that in diabetic rats without AG treatment (P<0.01). CONCLUSION: AG down-regulates renal Ang Ⅱ level, probably by reducing the formation of AGEs, which may be one of the renoprotective factors in diabetic nephropathy. More proofs are needed to identify the result that plasma AngⅡ concentration increases in DMA group.     

Effect of nitrogen and calcium stock plant nutrition on Petunia × hybrida leaf and anther explant growth in vitro

Petunia × hybrida Hort. Vilm.-Andr. ‘Coral Sea’ stock plants were grown with a modified Hoagland's solution to determine the effect of stock plant N and Ca nutrition on subsequent leaf explant and anther growth in vitro. In separate experiments, N was 0, 75, 150 or applied at 0, 100, 200 or 400 mg 1⁻¹ as nitrate-N, and Ca was applied at 300 mg 1⁻¹. Leaf explants from plants grown with 100 mg 1⁻¹ N produced the greatest amount of callus, while those from plants grown with 200 and 400 mg 1⁻¹ N produced the highest number of shoots. Nitrogen treatments increased the anther fresh weight and the number of shoots per culture compared to anthers derived from stock plants that did not receive N.The fresh weight of shoots produced by leaf explants decreased with increasing Ca concentrations applied to stock plants. Anthers derived from stock plants treated with 0 mg 1⁻¹ Ca produced the highest number of shoots per culture.Anatomically, both filament and anther wall tissue produced callus, but no callus production from microspores was observed. Organs produced by anthers were diploid.     

Inhibitory effect of ground dragon on the expression of α-SMA and FN in the lung tissue of mouse with asthma

AIM: To investigate the inhibitory effect of ground dragon on the expression of α-SMA and FN in the lung tissue with asthma. METHODS: The BALB/c mice were divided into four groups: control group (group A, n=20), asthmatic model group (group B, n=20), large-dose ground dragon treatment group (group C, n=20) and low-dose ground dragon treatment group (group D, n=20). To establish a mouse model of chronic asthma, we sensitized the mouse with 0.02% ovalbumin (OVA) by intraperitoneal injection, and stimulated the mice with 1% OVA by atomization. The treatment groups were given ground dragon before stimulation every time. After the last time of stimulation, the mice were subjected to laboratory tests. Inflammatory cells in bronchoalveolar lavage fluid were counted. Total level of IgE in serum was detected by ELISA. FN mRNA and α-SMA mRNA in the lung tissue were measured by RT-PCR and AlphaImager 2200 semi-quantitation analysis system. Expressions of FN and α-SMA were measured by the method of two-step immunohistochemistry and leica QWIN V3 analysis system. RESULTS: (1) Compared with those in group A, the expressions of α-SMA and FN in group B were significantly increased (P<0.01). Compared with group B, those in group C were significantly decreased (P<0.01), while those in group D were slightly decreased (P>0.05). (2) Compared with those in group A, the expression levels of α-SMA mRNA and FN mRNA in group B had a great increase (P<0.01). There was a notably decreases of α-SMA mRNA and FN mRNA levels in group C, compared with group B (P<0.01). However, α-SMA and FN mRNA level in group D was just a slightly decreased, compared with group B (P>0.05). CONCLUSION: The ground dragon inhibits α-SMA and FN expression in the lung tissue of mice with chronic asthma, indicating that ground dragon may inhibit airway remodeling in asthma through the inhibition of α-SMA and FN expressions.