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1.
Chin Med ; 19(1): 99, 2024 Jul 15.
Article in English | MEDLINE | ID: mdl-39010119

ABSTRACT

BACKGROUND: Allii Macrostemonis Bulbus is also named Xiebai in China. It is an edible vegetable, and also a famous herb for treating coronary heart disease. Allium chinense G. Don (ACGD) and Allium macrostemon Bunge (AMB) are it botanical sources. The aim of this study was to explore the cardioprotective effects, and decipher the visual spatial distribution and absolute content of primary metabolites derived from these two herbs. METHODS: H9c2 cells were used to perform the hypoxia-reoxygenation (H/R)-induced myocardial injury model. Their protective effects were evaluated by apoptosis levels. Furthermore, matrix-assisted laser desorption/ionization time-of-flight tandem mass spectrometry imaging approach (MALDI-TOF MSI) was carried out to present the spatial location of primary metabolites including fatty acids, amino acids, carotenoids, and vitamins in these two Allium herbs. Multiple analytical methods were applied to perform quantitative analysis of these primary metabolites in AMB and ACGD bulbs by liquid chromatography tandem mass spectrometry (LC-MS). RESULTS: First, AMB and ACGD extracts both could increase the cell viability in H9c2 cells, and attenuate H/R-induced injury. They markedly decreased apoptosis, accompanied by activating the BCL-2/BAX pathway. Further, MALDI-TOF MSI-based relative quantification results showed several amino acids, fatty acids, carotenoids, and vitamins were largely rich in the tunics and outside scales of fresh bulbs, while some primary metabolites were abundant in their developing flower buds. Absolute quantification results displayed total contents of amino acids in ACGD bulbs were higher than those in AMB, while total contents of fatty acids and vitamins provides opposite trends in these two Allium herbs. The total contents of carotenoids and trace elements showed no significant differences between AMB and ACGD samples. CONCLUSIONS: This study would be helpful to understand the myocardial injury protection effects of these two Allium herbs, and the spatial accumulation and quantitative content levels of their main nutrients.

2.
Biol Trace Elem Res ; 170(1): 146-51, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26206562

ABSTRACT

Cadmium (Cd) can induce bone loss and osteoporosis. Histologic methods have shown that Cd can induce microarchitecture change of the trabecular bone. The aim of this study is to evaluate the imaging biomarkers of osteoporosis induced by Cd using micro-computed tomography (micro-CT). Twenty-four male Sprague-Dawley rats were randomly divided into four groups that were exposed to Cd via drinking water at concentrations of 0, 2, 10, and 50 mg/L for 3 months. Before sacrifice, micro-CT scanning was performed on the proximal tibia. Three-dimensional images were analyzed by using commercial software to measure apparent bone mineral density (ABMD), tissue bone mineral density (TBMD), bone volume/total volume fraction (BV/TV), trabecular number (Tb.N), trabecular thickness (Tb.Th), trabecular separation (Tb.Sp), and structural model index (SMI) as imaging biomarkers. Histologic analyses were performed using hematoxylin and eosin (HE) and Goldner's trichrome stain. Exposure to Cd resulted in a marked decrease of ABMD, BV/TV, and Tb.N and an increase of Tb.Sp and SMI compared with control, especially for those treated with 50 mg Cd/L (p < 0.05). Decreased Tb.N and increased Tb.Sp compared to that of control were also observed in histologic findings. The micro-CT imaging is a promising tool for assessing the bone damage induced by Cd, and Tb.N, Tb.Sp, and SMI may be the potential sensitive imaging biomarkers.


Subject(s)
Biomarkers/metabolism , Bone and Bones/drug effects , Cadmium/toxicity , Environmental Exposure , Animals , Bone and Bones/metabolism , Male , Rats , Rats, Sprague-Dawley , X-Ray Microtomography
3.
Exp Ther Med ; 10(4): 1584-1590, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26622531

ABSTRACT

Acute lung injury (ALI) is characterized by severe lung edema and an increase in the inflammatory reaction. Considerable evidence has indicated that microRNAs (miRNAs or miRs) are involved in various human diseases; however, the expression profile and function of miRNAs in ALI have been rarely reported. The present study used miRNA microarray and reverse transcription-quantitative polymerase chain reaction to demonstrate that miR-181b is the one of the most significantly upregulated miRNA after lipopolysaccharide (LPS) stimulation in human bronchial epithelial cells, BEAS-2B. To elaborate the role of miR-181b in ALI, an assay was performed to investigate the overexpression of miR-181b in BEAS-2B cells, and the expression of inflammatory factors was then analyzed. The overexpression of miR-181b resulted in the induction of an increment in interleukin (IL)-6 levels. p65 was identified to be a primary component of NF-κB, since it was upregulated in the miR-181b overexpression in the BEAS-2B cells, while pyrrolidine dithiocarbamate, a specific inhibitor of NF-κB, was found to be able to abrogate the upregulation of the expression of p65. In conclusion, the findings of the present study suggested that miR-181b may be involved in the process of LPS-induced inflammation in BEAS-2B cells by activating the NF-κB signaling pathway, which implies that it may serve as a potential therapeutic target for ALI.

4.
Exp Ther Med ; 9(1): 143-146, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25452790

ABSTRACT

Tartrate-resistant acid phosphatase 5b (TRACP 5b) has been used as a biomarker of bone resorption and cancer metastasis. TRACP 5b has also been suggested to be a reliable marker of osteoclast number. In this study, the correlation of TRACP 5b level and osteoclast-like cell number was investigated in RAW 264.7 cells treated with receptor-activated nuclear factor κB ligand (RANKL). RAW 264.7 cells were cultured with α-MEM containing RANKL (40 ng/ml) for 3, 5 and 7 days. Osteoclast formation and TRACP 5b levels were determined by TRACP staining, scanning electron microscopy and enzyme-linked immunosorbent assay. The RAW 264.7 cells that were not exposed to RANKL did not secrete TRACP 5b. RANKL induced the RAW 264.7 cells to differentiate into osteoclasts and to secrete TRACP 5b. The TRACP 5b level in the RAW 264.7 cells treated with RANKL was significantly correlated with the number and volume of osteoclasts (r=0.95 and r=0.92, respectively; P<0.0001). TRACP 5b is a good marker of RANKL-induced osteoclast formation in RAW 264.7 cells. TRACP 5b analysis may be used as an alternative to osteoclast counting in vitro.

5.
J Cardiol ; 60(6): 495-502, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22948092

ABSTRACT

OBJECTIVE: To provide scientific evidence supporting the efficacy of forest bathing as a natural therapy for human hypertension. METHODS: Twenty-four elderly patients with essential hypertension were randomly divided into two groups of 12. One group was sent to a broad-leaved evergreen forest to experience a 7-day/7-night trip, and the other was sent to a city area in Hangzhou for control. Blood pressure indicators, cardiovascular disease-related pathological factors including endothelin-1, homocysteine, renin, angiotensinogen, angiotensin II, angiotensin II type 1 receptor, angiotensin II type 2 receptor as well as inflammatory cytokines interleukin-6 and tumor necrosis factor α were detected. Meanwhile, profile of mood states (POMS) evaluation was used to assess the change of mood state of subjects. In addition, the air quality in the two experimental sites was monitored during the 7-day duration, simultaneously. RESULTS: The baselines of the indicators of the subjects were not significantly different. Little alteration in the detected indicators in the city group was observed after the experiment. While subjects exposed to the forest environment showed a significant reduction in blood pressure in comparison to that of the city group. The values for the bio-indicators in subjects exposed to the forest environment were also lower than those in the urban control group and the baseline levels of themselves. POMS evaluation showed that the scores in the negative subscales were lowered after exposure to the forest environment. Besides, the air quality in the forest environment was much better than that of the urban area evidenced by the quantitative detection of negative ions and PM10 (particulate matter < 10 µm in aerodynamic diameter). CONCLUSION: Our results provided direct evidence that forest bathing has therapeutic effects on human hypertension and induces inhibition of the renin-angiotensin system and inflammation, and thus inspiring its preventive efficacy against cardiovascular disorders.


Subject(s)
Environment , Hypertension/therapy , Renin-Angiotensin System , Trees , Affect , Aged , Blood Pressure , Cardiovascular Diseases/etiology , Cardiovascular Diseases/prevention & control , Cities , Endothelin-1 , Homocysteine , Humans , Hypertension/metabolism , Hypertension/physiopathology , Hypertension/psychology , Inflammation/prevention & control , Interleukin-6 , Middle Aged , Treatment Outcome , Tumor Necrosis Factor-alpha
6.
Oxid Med Cell Longev ; 2012: 750963, 2012.
Article in English | MEDLINE | ID: mdl-22577492

ABSTRACT

The present paper was designed to investigate the effect of pine pollen against aging in human diploid fibroblast 2BS cells and in an accelerated aging model, which was established by subcutaneous injections with D-galactose daily for 8 weeks in C57BL/6J mice. Pine pollen (1 mg/mL and 2 mg/mL) is proved to delay the replicative senescence of 2BS cells as evidenced by enhanced cell proliferation, decreased SA-ß-Gal activity, and reversed expression of senescence-associated molecular markers, such as p53, p21(Waf1), p16(INK4a), PTEN, and p27(Kip1) in late PD cells. Besides, pine pollen reversed D-galactose-induced aging effects in neural activity and inflammatory cytokine levels, as indicated by improved memory latency time and reduced error rate in step-down test and decreased concentrations of IL-6 and TNF-α in model mice. Similar to the role of AGEs (advanced glycation endproducts) formation inhibitor aminoguanidine (AG), pine pollen inhibited D-galactose-induced increment of AGEs levels thus reversed the aging phenotypes in model mice. Furthermore, the declined antioxidant activity was obviously reversed upon pine pollen treatment, which may account for its inhibitory effect on nonenzymatic glycation (NEG) in vivo. Our finding presents pine pollen as an attractive agent with potential to retard aging and attenuate age-related diseases in humans.


Subject(s)
Aging/drug effects , Diploidy , Fibroblasts/cytology , Fibroblasts/drug effects , Galactose/pharmacology , Pinus/chemistry , Pollen/metabolism , Animals , Antioxidants/metabolism , Body Weight/drug effects , Cell Line , Cell Proliferation/drug effects , Cellular Senescence/drug effects , Cytokines/metabolism , Female , Fibroblasts/enzymology , Glycation End Products, Advanced/metabolism , Humans , Inflammation Mediators/metabolism , Lipid Peroxidation/drug effects , Malondialdehyde/metabolism , Mice , Mice, Inbred C57BL , Models, Animal , Nervous System/drug effects , Staining and Labeling , Superoxide Dismutase/metabolism , beta-Galactosidase/metabolism
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