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1.
Clin Microbiol Infect ; 26(8): 1069-1075, 2020 Aug.
Article in English | MEDLINE | ID: mdl-31904566

ABSTRACT

OBJECTIVES: Data from clinical trials of human papillomavirus (HPV) vaccines showed that women naïve (negative for both type-specific antibodies and DNA) to vaccine types would derive benefit from vaccination; therefore, an understanding of the proportion of naïve women in different age groups is important for developing HPV vaccination strategies. METHODS: From November 2012 to April 2013, a total of 7372 healthy women aged 18-45 years were recruited in five provinces in China. Cervical specimens and serum samples were collected for each woman at entry. Cervical specimens were first tested by the HPV DNA enzyme immunoassay method; if positive, the specimens were then tested by reverse hybridization line probe assay and HPV-16 and HPV-18 specific polymerase chain reactions. Neutralizing antibodies against HPV-16 or HPV-18 were tested with a pseudovirion-based neutralization assay. RESULTS: The overall prevalence of high-risk HPV DNA was 14.8% (1088/7367, 95% CI 14.0-15.6), and the seroprevalence of neutralizing antibodies against HPV-16 and HPV-18 was 12.6% (925/7367) and 4.9% (364/7367), respectively. In younger women (18-26 years) and middle-aged women (27-45 years), 83.8% (3116/3719) and 81.4% (2968/3648) were naïve to both HPV-16 and HPV-18 (both neutralizing antibodies and DNA were negative), respectively. In addition, 98.5% (3664/3719) and 98.0% (3575/3648) of the younger or middle-aged women were naïve to at least one HPV type (HPV-16 or HPV-18). DISCUSSION: This study revealed that the majority of Chinese women aged 18-26 years and 27-45 years were naïve to both HPV-16 and HPV-18 and would thus derive full benefit from bivalent HPV vaccination.


Subject(s)
Antibodies, Neutralizing/blood , Human papillomavirus 16/genetics , Human papillomavirus 18/genetics , Papillomavirus Infections/epidemiology , Adolescent , Adult , Age Distribution , Antibodies, Viral/blood , China/epidemiology , DNA, Viral/genetics , Double-Blind Method , Female , Human papillomavirus 16/immunology , Human papillomavirus 18/immunology , Humans , Middle Aged , Papillomavirus Infections/immunology , Prevalence , Young Adult
2.
Anim Genet ; 44(1): 79-85, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22524237

ABSTRACT

The domestic goat is one of the most important livestock species, but its origins and genetic diversity still remain uncertain. Multiple highly divergent maternal lineages of goat have been reported in previous studies. Although one of the mitochondrial DNA lineages, lineage B, was detected only in eastern and southern Asia, the geographic distribution of these lineages was previously unclear. Here, we examine the genetic diversity and phylogeographic structure of Asian goats by mitochondrial DNA sequences and morphological characteristics. The analyses of a total of 1661 Asian goats from 12 countries revealed a high frequency of lineage B in Southeast Asia. The frequency of this lineage tended to be higher in mountain areas than in plain areas in Southeast Asian countries, and there was a significant correlation between its frequency and morphological traits. The results suggest an original predominance of lineage B in Southeast Asia and the recent infiltration of lineage A into Southeast Asian goats.


Subject(s)
DNA, Mitochondrial/genetics , Genetic Variation , Goats/genetics , Phylogeography , Animals , Asia, Southeastern , DNA, Mitochondrial/blood , Asia, Eastern , Goats/anatomy & histology , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , Sequence Analysis, DNA , Sequence Homology
3.
Lupus ; 19(11): 1344-50, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20693192

ABSTRACT

The aim of the study was to investigate the characteristics and risk factors for hyperglycemia in Chinese female patients with systemic lupus erythematosus (SLE). One hundred and forty-six female SLE patients without a history of diabetes underwent a 75 g oral glucose tolerance test to evaluate glucose tolerance, insulin sensitivity and pancreatic beta cell function. According to the 1999 World Health Organization criteria, all patients were divided into three groups: normal glucose regulation, impaired glucose tolerance and diabetes mellitus. Glucocorticoid doses, insulin sensitivity and pancreatic beta cell function were compared among these groups. Risk factors for hyperglycemia were analyzed by univariate and multi-variate regression analysis. Our results showed that 46 of the 146 female SLE patients (31.5 %) were hyperglycemic, including 21 (14.4%) diabetes mellitus patients and 25 (17.1%) impaired glucose tolerance patients. These female SLE patients with hyperglycemia were characterized by insulin resistance and reduced pancreatic beta cell function, and they were relatively young. Age ≥35 years and high glucocorticoid doses were risk factors for hyperglycemia in Chinese female SLE patients. The prevalence of diabetes mellitus and impaired glucose tolerance are quite high in Chinese female SLE patients. It is suggested that plasma glucose concentration should be monitored regularly and oral glucose tolerance test should be recommended for SLE patients who have risk factors for hyperglycemia.


Subject(s)
Asian People , Hyperglycemia/etiology , Lupus Erythematosus, Systemic/complications , Adolescent , Adult , Blood Glucose/analysis , Diabetes Mellitus, Type 2/epidemiology , Diabetes Mellitus, Type 2/etiology , Female , Glucose Tolerance Test , Humans , Hyperglycemia/epidemiology , Insulin/blood , Insulin Resistance , Insulin-Secreting Cells/metabolism , Lupus Erythematosus, Systemic/epidemiology , Middle Aged , Risk Factors , Young Adult
4.
Acta Crystallogr C ; 57(Pt 3): 243-5, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11250562

ABSTRACT

The structure of the title compound, mu-hexavanadato(V)-bis[bis(2,2'-bipyridine)nickel(II)], [(Ni(C(10)H(8)N(2))(2))(2)(V(6)O(17))], is composed of vanadium oxide layers intercalated by complex [Ni(bipy)(2)](2+) cations (bipy is 2,2'-bipyridine). The structure is isomorphous with that reported recently for [Zn(bipy)(2)](2)[V(6)O(17)] [Zhang, DeBord, O'Connor, Haushalter, Clearfield & Zubieta (1996). Angew. Chem. Int. Ed. Engl. 35, 989--991]. The vanadium oxide layers are built up solely from VO(4) tetrahedra by corner sharing and clearly exhibit a sinusoidal ruffling. Two O atoms from a single vanadium oxide layer are coordinated to each Ni atom of the complex cations in a cis fashion, with Ni--O distances of 2.027 (3) and 2.087 (3) A, thus maintaining the two-dimensional structure.

5.
Am J Physiol Endocrinol Metab ; 279(3): E622-9, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10950831

ABSTRACT

Uncoupling protein 3 (UCP-3), a member of the mitochondrial transporter superfamily, is expressed primarily in skeletal muscle where it may play a role in altering metabolic function under conditions of fuel depletion caused, for example, by fasting and exercise. Here, we show that treadmill running by rats rapidly (30 min) induces skeletal muscle UCP-3 mRNA expression (sevenfold after 200 min), as do hypoxia and swimming in a comparably rapid and substantial fashion. The expression of the mitochondrial transporters, carnitine palmitoyltransferase 1 and the tricarboxylate carrier, is unaffected under these conditions. Hypoxia and exercise-mediated induction of UCP-3 mRNA result in a corresponding four- to sixfold increase in rat UCP-3 protein. We treated extensor digitorum longus (EDL) muscle with 5'-amino-4-imidazolecarboxamide ribonucleoside (AICAR), a compound that activates AMP-activated protein kinase (AMPK), an enzyme known to be stimulated during exercise and hypoxia. Incubation of rat EDL muscle in vitro for 30 min with 2 mM AICAR causes a threefold increase in UCP-3 mRNA and a 1.5-fold increase of UCP-3 protein compared with untreated muscle. These data are consistent with the notion that activation of AMPK, presumably as a result of fuel depletion, rapidly regulates UCP-3 gene expression.


Subject(s)
Carrier Proteins/biosynthesis , Hypoxia/metabolism , Multienzyme Complexes/metabolism , Muscle, Skeletal/metabolism , Physical Exertion/physiology , Protein Serine-Threonine Kinases/metabolism , AMP-Activated Protein Kinases , Animals , Blotting, Northern , DNA Probes/metabolism , Electrophoresis, Polyacrylamide Gel , Fatty Acids, Nonesterified/metabolism , Hypoxia/enzymology , In Vitro Techniques , Ion Channels , Male , Mitochondria, Muscle/enzymology , Mitochondria, Muscle/metabolism , Mitochondrial Proteins , Muscle Proteins/metabolism , Muscle, Skeletal/enzymology , RNA, Messenger/biosynthesis , RNA, Messenger/isolation & purification , Rats , Rats, Sprague-Dawley , Running/physiology , Swimming/physiology , Uncoupling Protein 3
6.
J Biol Chem ; 272(39): 24145-7, 1997 Sep 26.
Article in English | MEDLINE | ID: mdl-9305862

ABSTRACT

In fat and skeletal muscle cells, glucose transporter isoform 4 (Glut4) is translocated to the cell surface in response to insulin via a system of specialized recycling vesicles. Besides Glut4, these vesicles include the novel insulin-regulatable aminopeptidase, receptors for insulin-like growth factor-II/Man-6-phosphate and transferrin, and a glycoprotein with the molecular mass of 110 kDa. We report here by the criteria of the partial protein sequencing and subsequent cDNA cloning that glycoprotein 110, the last unidentified major protein component of Glut4-containing vesicles, is sortilin, a novel type I receptor-like protein recently cloned from human brain (Petersen, C. M., Nielsen, M. S., Nykjar, A., Jacobsen, L., Tommerup, N., Rasmussen, H. H., Roigaard, H., Gliemann, J., Madsen, P., and Moestrup, S. K. (1997) J. Biol. Chem. 272, 3599-3605). This protein is highly expressed in fat, brain, and lung and is dramatically up-regulated during differentiation of adipocytes in vitro.


Subject(s)
Membrane Glycoproteins/metabolism , Monosaccharide Transport Proteins/metabolism , Muscle Proteins , Nerve Tissue Proteins/metabolism , 3T3 Cells , Adaptor Proteins, Vesicular Transport , Adipocytes/metabolism , Amino Acid Sequence , Animals , DNA, Complementary , Glucose Transporter Type 4 , Humans , Male , Membrane Glycoproteins/genetics , Mice , Molecular Sequence Data , Monosaccharide Transport Proteins/chemistry , Nerve Tissue Proteins/genetics , Rats , Rats, Sprague-Dawley , Sequence Homology, Amino Acid
7.
Biochim Biophys Acta ; 1147(2): 237-44, 1993 Apr 22.
Article in English | MEDLINE | ID: mdl-8476917

ABSTRACT

The stability of small unilamellar vesicles (SUV) made from negatively-charged phosphatidate by ultrasonication or pH-jump has been investigated. As criteria for the vesicle stability are used: (I) the bilayer integrity as judged from the permeability of the fluorescent probe carboxyfluorescein (CF) and (II) the susceptibility of the phospholipid vesicles to fusion as judged by gel filtration and freeze-fracture electron microscopy. Egg phosphatidate SUV (PA-SUV) whose internal cavity is in equilibrium with the dispersion medium are strictly speaking thermodynamically unstable by these criteria. They may, however, be regarded as stable from a practical point of view. CF-release is observed with a half-time of 14 days and also some vesicle fusion, particularly at low temperature (4 degrees C). The small effects observed, e.g., the small tendency of the vesicles to undergo fusion is probably due to the high surface charge density of PA bilayers. A main finding of this work is that the same positive pH-gradient which is used in the pH-jump method to drive the formation of SUV from large phosphatidic acid bilayer sheets has a stabilizing effect on the resulting PA-SUV. Stabilization is achieved by positive pH-gradients of about two pH-units or more with the pH of the external medium exceeding the pH of the vesicle cavity. Under these conditions, up to about 8 weeks no significant loss of entrapped CF and no fusion of SUV was observed both at 4 degrees C and room temperature. In contrast, a reverse or negative pH-gradient of several pH units applied to PA-SUV (with the external pH being lower than that of the vesicle cavity) destabilizes PA-SUV. Such a gradient can be shown to lead to a dramatic perturbation of the lipid bilayer packing as evident from a significant increase in CF permeability. The local perturbation of the phospholipid bilayer is accompanied by massive vesicle fusion which is prominent at low temperature (4 degrees C).


Subject(s)
Lipid Bilayers/chemistry , Phospholipids/chemistry , Drug Stability , Fluoresceins , Hydrogen-Ion Concentration , Kinetics , Temperature , Thermodynamics
8.
Chem Phys Lipids ; 60(3): 209-23, 1992.
Article in English | MEDLINE | ID: mdl-1505061

ABSTRACT

The monolayer and thermal behaviour of different phosphatidic acids are presented. At neutral pH and 22 degrees C dilauroylphosphatidic acid and unsaturated phosphatidic acids form liquid-expanded monolayers, while dipalmitoyl- and distearoylphosphatidic acid form condensed monolayers. Dimyristoylphosphatidic acid undergoes a transition from the liquid-expanded to the condensed state. With long-chain saturated and unsaturated phosphatidic acids little change in molecular area is observed between pH 2 and 7. In contrast, the short chain saturated phosphatidic acids, dilauroyl- and dimyristoylphosphatidic acids, undergo a condensation in the pH range 2 to 7. This is so in spite of the fact that the phosphoric acid group dissociates and the phosphatidic acid molecule attains one negative charge over this pH range. This finding is interpreted to indicate that the electrostatic repulsion between negatively charged phosphatidic acid molecules is compensated for or even outweighed by other intermolecular forces. Hydrogen bonding at the lipid/water interface is supposed to play a major role. All phosphatidates studied exhibit a significant expansion in the pH range 7 to 12. The second apparent pK of the primary phosphate group of phosphatidic acids is 8.6 and the expansion observed in this pH range is therefore due to electrostatic repulsion. At neutral pH the ether analogues of saturated phosphatidic acids have monolayer properties similar to those of the ester compounds. Considering the total pH range of 2 to 12 studied the force-area curves of the ether analogues are more condensed compared to the ester compounds. Synthetic phosphatidates and their ether analogues give reversible sharp crystal(gel)-to-liquid crystal transitions while the naturally occurring egg phosphatidate gives a broad, asymmetric one. The transition temperature Tm of saturated phosphatidates increases with increasing hydrocarbon chain length and at a given chain length Tm decreases markedly with unsaturation. The Tm values of the ether analogues are about 10 degrees C higher and the delta H values are 10-15% lower than those of the corresponding esters.


Subject(s)
Phosphatidic Acids/chemistry , Calorimetry, Differential Scanning , Hot Temperature , Hydrogen-Ion Concentration , Temperature , Thermodynamics
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