Serum fibroblast growth factor-2 levels complement vital biomarkers for diagnosing heart failure.

BACKGROUND: Early diagnosis of atrial fibrillation is important as it is crucial for improving patient outcomes. Fibroblast growth factor-2 (FGF2) may serve as a diagnostic biomarker for heart failure due to its ability to promote cardiac fibrosis and hypertrophy; however, the relationship between FGF2 concentration and heart failure is unclear. Therefore, this study aimed to explore whether FGF2 could aid in distinguishing patients with heart failure from healthy controls and those with dyspnea without heart failure. Additionally, to evaluate the possible correlation between serum FGF2 levels and its diagnostic parameters in patients with heart failure. METHODS: Plasma FGF2 concentration was measured in 114 patients with a complaint of dyspnea (enrolled in the study between January 2022 and August 2022). Based on heart failure diagnosis, the patients were assigned to three groups, as follows: heart failure (n = 80), non-heart-failure dyspnea (n = 34), and healthy controls (n = 36), following physical examination. Possible correlations between serum FGF2 levels and other prognostic parameters in patients with heart failure were analyzed. RESULTS: Serum FGF2 levels were higher in patients with heart failure (125.60 [88.95, 183.40] pg/mL) than in those with non-heart-failure dyspnea (65.30 [28.85, 78.95] pg/mL) and healthy controls (78.90 [60.80, 87.20] pg/mL) (p < 0.001). Receiver operating characteristic curve analysis identified FGF2 concentration as a significant predictor in heart failure diagnosis, with an area under the curve of 0.8693 (p < 0.0001). Importantly, in the heart failure group, serum FGF2 concentrations correlated with key prognostic parameters for heart failure, such as reduced left ventricular ejection fraction and elevated serum levels of N-terminal pro-B-type natriuretic peptide. CONCLUSIONS: Elevated serum FGF2 level is strongly associated with an increased risk of heart failure and could serve as a useful biomarker to complement vital diagnostic parameters for heart failure.

Hypertonic saline activates CD4+ and CD8+ T-lymphocytes in the small intestine to alleviate intestinal ischemia-reperfusion injury.

OBJECTIVE: Intestinal ischemia-reperfusion injury (I/R) is a common syndrome encountered in clinic following intestinal surgery, strangulated hernia, and shock. Hypertonic saline has been shown to prevent inflammatory tissue damages caused by I/R and regulate immunologic disorders in peripheral blood. However, the immunoregulatory effects of hypertonic saline on the small intestine response to intestinal I/R have not been reported. MATERIALS AND METHODS: To investigate this, we created the intestinal I/R model by clamping the superior mesenteric artery in Sprague-Dawley rats. After 1 hour of ischemia, the vascular clamp was removed, and either normal saline (0.9% NaCl, NS group) or hypertonic saline (7.5% NaCl, HS group) was administered through the tail vein (6 ml/kg). The CD4(+) and CD(8+), primarily T-lymphocytes subpopulation yielded from the intestinal tissues, were determined by immunohistochemistry. RESULTS: A pro-inflammatory cytokine, tumor necrosis factor (TNF)-α, and nuclear factor kappa B (NF-κB), a critical transcription factor for the TNF-α gene, were measured in the intestinal and lung tissues with ELISA. HS induced an increase in CD4(+) and CD8(+) T cells in the jejunum and ileum compared with the NS group. The levels of TNF-α and NF-κB in the intestinal and lung tissues were significantly decreased in the HS group compared with those of the NS group. CONCLUSIONS: HS treatment may ameliorate the tissue damage induced by intestinal I/R. This protective effect is possibly due to its ability to activate the CD4(+) and CD8(+) T-lymphocytes cells in the intestinal tissues and inhibit the intestinal I/R-induced expression of pro-inflammatory cytokines.

Fractional iron solubility of aerosol particles enhanced by biomass burning and ship emission in Shanghai, East China.

In terms of understanding Fe mobilization from aerosol particles in East China, the PM2.5 particles were collected in spring at Shanghai. Combined with the backtrajectory analysis, the PM2.5/PM10 and Ca/Al ratios, a serious dust-storm episode (DSE) during the sampling was identified. The single-particle analysis showed that the major iron-bearing class is the aluminosilicate dust during DSE, while the Fe-bearing aerosols are dominated by coal fly ash, followed by a minority of iron oxides during the non-dust storm days (NDS). Chemical analyses of samples showed that the fractional Fe solubility (%FeS) is much higher during NDS than that during DSE, and a strong inverse relationship of R(2)=0.967 between %FeS and total atmospheric iron loading were found, suggested that total Fe (FeT) is not controlling soluble Fe (FeS) during the sampling. Furthermore, no relationship between FeS and any of acidic species was established, suggesting that acidic process on aerosol surfaces are not involved in the trend of iron solubility. It was thus proposed that the source-dependent composition of aerosol particles is a primary determinant for %FeS. Specially, the Al/Fe ratio is poorly correlated (R(2)=0.113) with %FeS, while the apparent relationship between %FeS and the calculated KBB(+)/Fe ratio (R(2)=0.888) and the V/Fe ratio (R(2)=0.736) were observed, reflecting that %FeS could be controlled by both biomass burning and oil ash from ship emission, rather than mineral particles and coal fly ash, although the latter two are the main contributors to the atmospheric Fe loading during the sampling. Such information can be useful improving our understanding on iron solubility on East China, which may further correlate with iron bioavailability to the ocean, as well as human health effects associated with exposure to fine Fe-rich particles in densely populated metropolis in China.

First Report of Target Leaf Spot Caused by Corynespora cassiicola on Cowpea in China.

Cowpea (Vigna unguiculata L.) is an important economic vegetable and is widely planted in China. During a survey of diseases in May 2009, a new leaf disease incited by the fungus Corynespora cassiicola was observed on cowpea growing in greenhouses in Shouguang city, Shandong Province, China. Circular lesions of different sizes were present on approximately 40% of the plants. Lesions were round with grayish brown centers surrounded by brownish concentric rings and ranged from 1 to 13 mm in diameter. Leaves with many lesions resulted in chlorosis, wilt, and defoliation. Yellow disk was observed on lesion edges of partly infected leaves. Abundant conidia and conidiophores appeared on the abaxial surface of leaves. To identify the causal pathogen, pieces of tissue from the leading border of lesions were sterilized in 75% ethanol for 1 min, rinsed in sterile water, transferred to potato dextrose agar (PDA), and then incubated at 28°C in an incubator. Colonies grew to 60 mm and were gray in color after 7 days. Conidiophores were straight and unbranched, pale or dark brown, and 63 to 211 × 4 to 8 µm. Conidia were born singly or in chains, obclavate or cylindrical, brown or olivaceous, 33 to 97 × 5 to 11 µm. Based on the above characteristics, the fungus was similar to C. cassiicola (Berk. & M.A. Curtis.) C.T. Wei (2). The internal transcribed spacer (ITS) region of rDNA was amplified using primers ITS1 and ITS2 and deposited in GenBank (Accession No. KC894915). A BLAST search in GenBank indicated precise match for a sequence of C. cassiicola from cowpea in American Samoa (1). To satisfy Koch's postulates, 20 one-month-old seedlings of cowpea were sprayed with a spore suspension (1 × 105 spores/ml) of one isolate of C. cassiicola until runoff. Another 20 seedlings, sprayed with sterile water, served as non-inoculated controls. Plants were placed in a humidity chamber at 28°C for 12 h and then transferred to a growth chamber at 28°C. Symptoms similar to those described above appeared after 7 days on inoculated plants; however, no symptoms were observed on non-inoculated controls. C. cassiicola was re-isolated from inoculated plants. The pathogen can cause diseases on a number of plants and lead to losses. In China, this pathogen has previously been recorded on about 20 genera of plants. It also included V. sinensis (3), a close plant with V. unguiculata. However, to our knowledge, this is the first report of target leaf spot caused by C. cassiicola on cowpea (V. unguiculata) in China. Control measures may be needed to manage the disease. References: (1) L. J. Dixon et al. Phytopathology 99:1015, 2009. (2) M. B. Ellis. CMI Mycol. Pap. No. 65, 1957. (3) F. L. Tai. Sylloge Fungorum Sinicorum. Science Press, Beijing, 1979.

IR plus vacuum ultraviolet spectroscopy of neutral and ionic organic acid molecules and clusters: acetic acid.

Infrared (IR) vibrational spectroscopy of acetic acid (A) neutral and ionic monomers and clusters, employing vacuum ultraviolet (VUV), 10.5 eV single photon ionization of supersonically expanded and cooled acetic acid samples, is presented and discussed. Molecular and cluster species are identified by time of flight mass spectroscopy: the major mass features observed are A(n)H(+) (n=1-9), ACOOH(+) (VUV ionization) without IR radiation present, and A(+) with both IR and VUV radiation present. The intense feature ACOOH(+) arises from the cleavage of (A)(2) at the beta-CC bond to generate ACOOH(+)+CH(3) following ionization. The vibrational spectrum of monomeric acetic acid (2500-7500 cm(-1)) is measured by nonresonant ionization detected infrared (NRID-IR) spectroscopy. The fundamentals and overtones of the CH and OH stretches and some combination bands are identified in the spectrum. Mass selected IR spectra of neutral and cationic acetic acid clusters are measured in the 2500-3800 cm(-1) range employing nonresonant ionization dip-IR and IR photodissociation (IRPD) spectroscopies, respectively. Characteristic bands observed at approximately 2500-2900 cm(-1) for the cyclic ring dimer are identified and tentatively assigned. For large neutral acetic acid clusters A(n)(n>2), spectra display only hydrogen bonded OH stretch features, while the CH modes (2500-2900 cm(-1)) do not change with cluster size n. The IRPD spectra of protonated (cationic) acetic acid clusters A(n)H(+) (n=1-7) exhibit a blueshift of the free OH stretch with increasing n. These bands finally disappear for n> or =6, and one broad and weak band due to hydrogen bonded OH stretch vibrations at approximately 3350 cm(-1) is detected. These results indicate that at least one OH group is not involved in the hydrogen bonding network for the smaller (n< or =5) A(n)H(+) species. The disappearance of the free OH stretch feature at n> or =6 suggests that closed cyclic structures form for A(n)H(+) for the larger clusters (n> or =6).

IR plus vacuum ultraviolet spectroscopy of neutral and ionic organic acid monomers and clusters: propanoic acid.

The vibrational spectrum of molecular propanoic acid, cooled in a supersonic expansion, in the region of 2500 to 7500 cm(-1) is obtained employing infrared plus vacuum ultraviolet nonresonant ionization detected spectroscopy. The fundamental and first overtone of the CH and OH stretch modes of cold propanoic acid molecules can be identified in the spectrum. Propanoic acid neutral and ionic clusters are also studied employing nonresonant ion dip and photodissociation spectroscopic techniques, respectively. For the neutral dimer, a sequence of features observed at ca. 2500-2700 cm(-1) can be assigned as combination bands of low frequency modes with the COH bending overtone; these features characterize the cyclic dimer ring structure. IR spectra of the larger neutral clusters n=3, 4, 5 indicate that they also have cyclic structures in which the OH groups are engaged in the cluster hydrogen bonding network. The CH groups are not involved in this hydrogen bonding structure. Free OH features are observed for the protonated ion clusters (C(2)H(5)COOH)(n)H(+), n=1,...,5, indicating that at least one OH group of these cluster ions is not involved in the cluster hydrogen bonding network. A comparison of the results for four hydrogen bonding neutral and ionic clusters (CH(3)OH, C(2)H(5)OH, CH(3)COOH, and C(2)H(5)COOH) is presented and discussed.

Infrared plus vacuum ultraviolet spectroscopy of neutral and ionic ethanol monomers and clusters.

A high sensitivity spectroscopy is employed to detect vibrational antiitions of ethanol neutrals and ions in a supersonic expansion. The infrared (IR) features located at 3682 and 3667 cm(-1) can be assigned to the OH stretch for the two neutral C(2)H(5)OH conformers, anti and gauche, respectively. Their overtone energies located at 7179 (anti) and 7141 (gauche) cm(-1) are also identified. The OH fundamental stretch for ethanol ions is redshifted around 210 cm(-1), while the CH stretch modes are unchanged for neutral and ionic C(2)H(5)OH at around 2900-3000 cm(-1). The charge on the ethanol ion is apparently localized on the oxygen atom. IR induced photodissociation spectroscopy is applied to the study of neutral and protonated ethanol clusters. Neutral and protonated ethanol cluster vibrations are observed. The CH modes are not perturbed by the clustering process. Neutral clusters display only hydrogen bonded OH features, while the protonated ionic clusters display both hydrogen bonded and non-hydrogen-bonded features. These spectroscopic results are analyzed to obtain qualitative structural information on neutral and ionic ethanol clusters.

Infrared plus vacuum ultraviolet spectroscopy of neutral and ionic methanol monomers and clusters: new experimental results.

We present new observations of the infrared (IR) spectrum of neutral methanol and neutral and protonated methanol clusters employing IR plus vacuum ultraviolet (vuv) spectroscopic techniques. The tunable IR light covers the energy ranges of 2500-4500 cm(-1) and 5000-7500 cm(-1). The CH and OH fundamental stretch modes, the OH overtone mode, and combination bands are identified in the vibrational spectrum of supersonic expansion cooled methanol (2500-7500 cm(-1)). Cluster size selected IR plus vuv nonresonant infrared ion-dip infrared spectra of neutral methanol clusters, (CH(3)OH)(n) (n=2,[ellipsis (horizontal)],8), demonstrate that the methanol dimer has free and bonded OH stretch features, while clusters larger than the dimer display only hydrogen bonded OH stretch features. CH stretch mode spectra do not change with cluster size. These results suggest that all clusters larger than the dimer have a cyclic structure with OH groups involved in hydrogen bonding. CH groups are apparently not part of this cyclic binding network. Studies of protonated methanol cluster ions (CH(3)OH)(n)H(+) n=1,[ellipsis (horizontal)],7 are performed by size selected vuv plus IR photodissociation spectroscopy in the OH and CH stretch regions. Energies of the free and hydrogen bonded OH stretches exhibit blueshifts with increasing n, and these two modes converge to approximately 3670 and 3400 cm(-1) at cluster size n=7, respectively.

Generation and detection of alkyl peroxy radicals in a supersonic jet expansion.

Alkyl peroxy radicals are synthesized in a supersonic jet expansion by the initial production of alkyl radicals and subsequent reaction with molecular oxygen. Parent ions CH3OO+/CD3OO+ are observed employing vacuum ultraviolet (VUV) single photon ionizationtime-of-flight mass spectroscopy (TOFMS). Employing infrared (IR) + VUV photofragmentation detected spectroscopy, rotationally resolved infrared spectra of jet-cooled CH3OO and CD3OO radicals are recorded for the A 2A' <-- X 2A" transition by scanning the IR laser frequency while monitoring the CH3 + and CD3 + ion signals generated by the VUV laser. The band origins of the A 2A'<--X 2A" transition for CH3OO and CD3OO are identified at 7381 and 7371 cm(-1), respectively. Rotational simulation for the CH3OO and CD3OO 0(0) 0 transitions of A<--X yields a rotational temperature for these radicals of approximately 30 K. With the aid of ab initio calculations, two and five vibrational modes for the A 2A' excited electronic state are assigned for CH3OO and CD3OO radicals, respectively. Both experimental and theoretical results suggest that the ground electronic state of the ions of ethyl and propyl peroxy radicals are not stable although their ionization energies (IE) are less than 10.5 eV. The C2H5OO+/C3H7OO+ cations can readily decompose to C2H5 +/C3H7 + and O2. This is partially responsible for the inability of IR+VUV photofragmentation spectroscopy to detect the near IR A<--X electronic transition for these radicals.

Vibronic spectroscopy of the peroxyacetyl radical in the near IR.

The A 2A'<--X 2A" electronic transition of the peroxyacetyl radical (PA) is observed employing NIR/VUV ion enhancement, supersonic jet spectroscopy. Rotational envelope simulations yield a rotational temperature for ground state PA of ca. 55 K. Ab initio calculations of transition energies and vibrational frequencies for the A<--X transition assist in the assignment of the observed spectrum. A number of the vibrational modes of the A state are assigned to observed transitions (the O-O stretch 2(1), the COO bend 5(1), and the CCOO backbone bend 6(1)). The calculations and mass spectra suggest that the ground state of the PA ion is repulsive. An increase in rotational linewidth of the overtone of the O-O stretch (2(1)) is observed and discussed in terms of A state dynamics. The O-O stretch anharmonicity is estimated to be 13.35 cm(-1).

Generation and detection of the peroxyacetyl radical in the pyrolysis of peroxyacetyl nitrate in a supersonic expansion.

The peroxyacetyl radical (PA, CH3C(O)OO) is generated by flash pyrolysis of peroxyacetyl nitrate (PAN, CH3C(O)OONO2) in a supersonic jet. The 0(0)(0) A2A' <-- X2A'' electronic transition for PA, at ca. 5582 cm(-1), is detected in a supersonically cooled sample by time-of-flight mass spectroscopy in the CH3CO mass channel. Rotational envelope simulation results find that the rotational temperature for PA in its ground electronic and vibrational state is ca. 55 K. At ca. 330 degrees C, the thermal decomposition of PAN by flash pyrolysis in a heated nozzle with supersonic expansion is mainly by formation of PA and NO2. The maximum yield of PA is obtained at this temperature. At higher temperatures (300-550 degrees C), an intense signal in the CH2CO+ mass channel is observed, generated by the decomposition of PA.

IR+vacuum ultraviolet (118 nm) nonresonant ionization spectroscopy of methanol monomers and clusters: neutral cluster distribution and size-specific detection of the OH stretch vibrations.

Small methanol clusters are formed by expanding a mixture of methanol vapor seeded in helium and are detected using vacuum UV (vuv) (118 nm) single-photon ionization/linear time-of-flight mass spectrometer (TOFMS). Protonated cluster ions, (CH3OH)(n-1)H+ (n=2-8), formed through intracluster ion-molecule reactions following ionization, essentially correlate to the neutral clusters, (CH3OH)n, in the present study using 118 nm light as the ionization source. Both experimental and Born-Haber calculational results clarify that not enough excess energy is released into protonated cluster ions to initiate further fragmentation in the time scale appropriate for linear TOFMS. Size-specific spectra for (CH3OH)n (n=4 to 8) clusters in the OH stretch fundamental region are recorded by IR+vuv (118 nm) nonresonant ion-dip spectroscopy through the detection chain of IR multiphoton predissociation and subsequent vuv single-photon ionization. The general structures and gross features of these cluster spectra are consistent with previous theoretical calculations. The lowest-energy peak contributed to each cluster spectrum is redshifted with increasing cluster size from n=4 to 8, and limits near approximately 3220 cm(-1) in the heptamer and octamer. Moreover, IR+vuv nonresonant ionization detected spectroscopy is employed to study the OH stretch first overtone of the methanol monomer. The rotational temperature of the clusters is estimated to be at least 50 K based on the simulation of the monomer rotational envelope under clustering conditions.

IR/UV double resonant spectroscopy of the methyl radical: determination of nu3 in the 3p(z) Rydberg state.

IR+UV double resonant ion-dip and ion-enhancement spectroscopies are employed to study the nu3 asymmetric CH stretch vibration fundamental of CH3 in the ground and 3p(z) Rydberg electronic states. CH3 radical is synthesized in the supersonic jet expansion by flash pyrolysis of azomethane (CH3NNCH3) prior to the expansion. The Q band of the 3(1) (1) 3p(z)<--X transition of CH3, not detected by conventional UV resonantly enhanced multiphoton ionization (REMPI) spectroscopy, is determined to lie at 59,898 cm(-1) using IR+UV REMPI spectroscopy. Energy of the asymmetric CH stretch of CH3 in the 3p(z) Rydberg state, nu3(3p(z)), is 3087 cm(-1), redshifted by approximately 74 cm(-1) with respect to ground state nu3(X).

[The observation of the acute toxicity of the lanthanum and cerium to the buccal mucosa and systemic conditions of mice]

OBJECTIVE:The present study was to investigate the systemic and local acute toxicity of the lanthanum(La) and cerium(Ce) to the mice. METHODS: 0.2% and 1% La and Ce solutions were applied to buccal mucoa of mice.The systemic conditions and local histopathological changes were observed. RESULTS: The mice hadn't any systemic acute toxic reactions. Histological observation found that mucosal structures of most mice were almost normal,only a few mice showed the slight inflammation,but there were no significant differences between experimental and control groups. CONCLUSION: It was safe for local use of 0.2%,1% La and Ce to the buccal mucosa of mice. La and Ce may become a kind of safe caries-preventive drugs for local application.

[Immunohistochemical detection of PCNA and p53 protein in the premalignant lesions and squamous cell carcinomas of the oral mucosa]

PCNA and p53 protein expression were detected by immunohistochemical technique in 39 oral premalignant and malignant lesion;which included 11 oral mucosal leukoplakia(LK),9 oral lichen planus (LP),7 in situ carcinomas(ISC) and 12 squamous cell carcinomas(SCC);in order to investigate the significance of PCNA and p53 Protein overexpression in predicting malignant transformation.The results showed that the gradual strong expression of PCNA and mutated p53 protein positive signal from premalignant to malignant lesions.The remarkable correlation were found on PCNA expression between LK and ISC; on p53 protein expression between SCC I grade and SCC II grade and on PCNA and p53 protein expression between premalignant and malignant lesions.The results imply that expression of PCNA and mutated p53 protein may be as indicators for potential malignant development in benign lesions of oral mucosa premalignant.

[Histopathological and ultrastructural studies of melanomatic neuroectodermal tumor of infancy]

Three cases of melanomatic neuroectodermal tumor of infancy(MNTI) were studied.The tumor mainly consisted of small neuroblastic-like cells and pigmented large cuboidal cell,and infiltrated adjacent tissues.The main ultrastructural charactristics were the presence of some membranebound dense-core secretory granules,numerous free ribosomes and polysomes aggregaed in rosettes,occasional mitoses in the small cells;and four types of membranebound pigment granules corresponding to melanosomes at different stages of maturation in the pigment cell.immunohistochemical results indicated that both of main cells were positive reaction for NSE,negative for S-100.These facts suggested they are immature in and malignancy.Further,the isogenesis of the tumor cells and embryo optic cup cells were discussed.