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Biomedical subjects

Yi Cao

Publications and source records attributed to Yi Cao.

At least 37 records · Page 2Linked to original sources
PubMed2005

Novel amorphous functional materials for trapping nitrosamines.

Novel amorphous functional materials are designed to modify amorphous silica with alumina. They are first presented as efficient adsorbents to trap both volatile nitrosamines and bulky tobacco specific nitrosamines in the environment. Selective adsorption, temperature programmed surface reaction (TPSR), and FTIR methods are employed to study the impact of alumina modification on the ability of silica to adsorb and catalytically degrade nitrosamines. Due to the special interaction between the N-NO group of nitrosamines and the aluminum ion in the composite, nitrosamines can be very easily trapped by the composite. Moreover, this cost-efficient material first shows a remarkable adsorptive capability and catalytic activity in reduction of NNN (N-nitrosonornicotine) in the liquid phase. The new concept of designing a multifunctional trap for carcinogenic pollutants, which combines the amorphous silica's pore structure with the specific adsorbing/catalyzing features of metal ions, proves feasible.

Adsorption↗
PubMed2005

Core suture purchase affects strength of tendon repairs.

PURPOSE: It generally is considered that a certain distance should be maintained between the site of the tendon-suture junction and the laceration level of the tendon. In this study we assessed how the length of core suture purchase may affect the repair strength of transversely cut tendons using a 2-strand modified Kessler method and a 4-strand circle-locking method. METHODS: Seventy-four fresh pig flexor tendons were transected. Fifty-eight tendons were divided into 4 groups and repaired with a 2-strand grasping repair technique with the core suture purchase in the tendon stump ranging from 0.4 to 1.2 cm. Sixteen tendons were repaired with a 4-strand circle-locking tendon-suture repair technique. The core suture purchase of these tendons was 0.4 and 1.0 cm, respectively. The tendons were subjected to a linear, noncyclic, load-to-failure test in a tensile testing machine. The forces measured for initial gap formation, 2-mm gap formation, and ultimate strength were recorded for each repair. RESULTS: The resistance to gap formation and ultimate strength of 2-strand grasping technique repairs increased significantly as the suture purchase increased from 0.4 to 0.7, 1.0, and 1.2 cm although strength remained constant from 0.7 to 1.2 cm. The strength of 4-strand circle-locking repairs with a suture purchase of 1.0 cm was statistically greater than that of the repairs with a suture purchase of 0.4 cm. CONCLUSIONS: For both the 2-strand grasping and 4-strand circle-locking repair methods, the length of core suture purchase significantly influences the resistance to 2-mm gap formation and the ultimate strength of repairs in transversely lacerated flexor tendons. We determined that the optimal length of purchase is between 0.7 and 1.0 cm and that increased length of purchase from 0.7 to 1.2 cm does not increase the strength of the repair. Core suture purchase length of 0.4 cm or less results in significantly weaker repairs.

Animals↗
PubMed2005

Investigation of resistance of digital subcutaneous edema to gliding of the flexor tendon: an in vitro study.

PURPOSE: Although edema generally is considered to contribute to resistance to tendon mobilization and is a cause of tendon overload during postoperative motion exercise, it is unclear exactly how edema of the peritendinous tissues affects tendon mobilization. We assessed the effects of simulated subcutaneous edema on the gliding resistance of the flexor tendon in an in vitro model using chicken toes. METHODS: Thirty long toes of white Leghorn chickens were used. Twenty-two toes were divided into 2 groups and another 8 toes were used to determine the preconditions needed. In group 1 we produced 3 levels of edema severity in the subcutaneous tissue over a 1-cm segment by means of saline injection. In group 2 we created moderate tissue edema over 1-cm, 2-cm, or 3-cm segments of the toes. The work required to move the flexor digitorum profundus tendon over a fixed excursion and ultimate force were recorded with a testing machine after each run of flexion. RESULTS: Work and ultimate force increased significantly in the toes with simulated tissue edema in proportion to the severity and area of the edema. Even the least severe edema increased the work and force; a further increase to moderate edema tripled the energy needed to flex the toes. Increases in edema from 1-cm to a 2-cm and then to a 3-cm toe segment increased the work and force for each increment of extension. CONCLUSIONS: Simulated edema significantly increases energy and force required to move the tendons. The increase in resistance was proportionate to the severity and area of the edema. These results suggest that postoperative edema may increase significantly the resistance to tendon motion and that limiting both the severity and size of edema likely will reduce the resistance.

Animals↗
PubMed2005

Caspase-1 inhibitor Ac-YVAD-CHO attenuates quinolinic acid-induced increases in p53 and apoptosis in rat striatum.

AIM: To study the effects of the caspase-1 inhibitor Ac-YVAD-CHO on quinolinic acid (QA)-induced apoptosis. METHODS: Rats were pre-treated with intrastriatal infusion of Ac-YVAD-CHO (2-8 microg) before intrastriatal injection of QA (60 nmol). Striatal total proteins, genomic DNA, and nuclear proteins were isolated. The effects of Ac-YVAD-CHO on QA-induced caspase-1 activity, internucleosomal DNA fragmentation, IkappaB-alpha degradation, NF-kappaB, and AP-1 activation, and increases in p53 protein levels were measured with enzyme assays, agarose gel electrophoresis, electrophoresis mobility shift assays, and Western blot analysis. RESULTS: Pre-treatment with Ac-YVAD-CHO inhibited QA-induced internucleosomal DNA fragmentation. Ac-YVAD-CHO inhibited QA-induced increases in caspase-1 activity and p53 protein levels, but had no effect on QA-induced IkappaB-alpha degradation, NF-kappaB or AP-1 activation. CONCLUSION: Caspase-1 is involved in QA-induced p53 upregulation but not IkappaB-alpha degradation. Inhibition of caspase-1 attenuates QA-induced apoptosis in rat striatum.

Animals↗
PubMed2005

[Reactivity of pulmonary arteries and thoracic aortae in rats under tail-suspension and the effects of NOS inhibitor].

OBJECTIVE: To further disclose mechanisms in adaptation of pulmonary and systemic arteries to simulated microgravity (SM), so as to elucidate the mechanisms accounting for orthostatic intolerance after SM, and to explore a new kind of countermeasure for orthostatic intolerance. METHOD: 300 tail suspended (TS) rats were used as the model to simulate the physiological effects of microgravity. Vasoreactivity changes of rings sectioned from pulmonary artery (PA) and thoracic aorta (TA) to 68 mmoles/L KCl, plus phenylephrine (PE) and acetylcholine (ACh) were observed after 7 d and 14 d tail-suspension. After preconditioning with 10(-5) moles/L N-nitro-L-arginine methyl ester (L-NAME) for 20 min, vasoreactivity changes of PA and TA to PE and ACh were respectively repeated. RESULT: The contractile responsiveness of PA and TA to KCl and PE decreased significantly or very significantly after TS7 d and TSI4 d. The dilatory reactivity of PA and TA to ACh after TS7 d had a significant or very significant increase, but reactivity of PA showed no change and TA showed only a tendency to increase after TS14 d. After preconditioning with 10(-5) moles/L L-NAME, responsiveness of PA to PE after TS7 d and TS14 d had no difference among the three groups, but responsiveness of TA to PE after TS7 d and TS14 d had a significant decrease. The dilatory reactivity of PA after TS7 d decreased significantly or very significantly, and the remains showed no significant change. CONCLUSION: The decrease of contractile responsiveness of PA and TA might be due to the increased dilatory function of the endothelial cells. The fact that 10(-5) moles/L L-NAME reversed the decrease of contractile responsiveness of PA and partly of TA after tail suspension implicates that there might be an inhibitory action on the dilatory function of the endothelial cells. The NOS inhibitors may be helpful in preventing orthostatic intolerance.

Acetylcholine↗
PubMed2005

[The Doppler fetal heart rate detection with wavelet transform].

Various interference and noises should be eliminated while picking up the signal of fetal heart rate from the Doppler fetal signal in order to obtain smooth curve of the fetal heart Doppler signal and so to figure out the fetal heart rate. In this study, the mean frequency shift curve estimated from the Doppler fetal signals was smoothed using wavelet transform. The results showed that the fetal-heart rate obtained by computing from the autocorrelation waveform based on the smoothed mean frequency shift curve was more accurate than that based on unsmoothed curve.

Female↗
PubMed2005

[The curative effect of pulmonary surfactant on otitis media with effusion in guinea pigs].

OBJECTIVE: To find a new way of treating otitis media with effusion by studying the curative effect of pulmonary surfactant on secretory otitis media in guinea pigs. METHOD: Nonviable heat-killed pneumococci (HKP) solution was inoculated into the middle ear cavity in guinea pig via a transeardrum approach, set up models of otitis media with effusion in guinea pigs, after being injected with pulmonary surfactant by transeardrum approach, observed changes of serous effusion in tympanum and response threshold. RESULT: Five days after inoculation of HKB, serous effusion was present in the middle ear cavity of guinea pigs with disappearance of light cone. ABR response threshold raised from (14.00 +/- 3.08) dB to (45.00 +/- 5.67) dB. After seven days following injection of pulmonary surfactant by transeardrum approach, serous effusion of tympanum reduced or disappeared. ABR response threshold decreased from (45.00 +/- 5.67) dB to (23.53 +/- 6.32) dB, there was significantly difference between them (P < 0.001). In guinea pigs suffering from otitis media with effusion were not treated by PS, the serous effusion of tympanum did'nt change. Eardrum was more muddy and ABR response threshold raised from (45.00 +/- 5.67) dB before treatment (65.50 +/- 6.85) dB after being treated by PS, respectively, with statistically significant difference between them (P < 0.01). CONCLUSION: Pulmonary surfactant plays an important role in treating otitis media with effusion in guinea pigs.

Animals↗
PubMed2004

[Cloning and expression of aldolase encoding gene of Plasmodium falciparum FCC1/HN strain].

OBJECTIVE: To clone, sequence, and express the aldolase (ALD) encoding gene of Plasmodium falciparum FCC1/HN strain. METHODS: The ALD encoding gene was amplified by PCR from genomic DNA of FCC1/HN strain. The positive clones were screened and identified by agarose gel electrophoresis and endonuclease. The recombinant plasmid was transformed into E. coli M15. The fusion protein was expressed by IPTG induction and purified by Ni-NTA affinity chromatography and anion exchange column. RESULTS: The ALD gene of P. falciparum was amplified. Analysis of sequencing showed that the ALD gene of P. falciparum was identical with the sequence of other reported isolates. A Mr 41,000 fusion protein was induced by IPTG and was purified by chromatography. CONCLUSION: The ALD gene of P. falciparum FCC1/HN strain was identical to the other reported isolates. ALD fusion protein of P. falciparum was expressed and purified.

Amino Acid Sequence↗
PubMed2003

Role of metalloprotease disintegrin ADAM12 in determination of quiescent reserve cells during myogenic differentiation in vitro.

Skeletal myoblasts grown in vitro and induced to differentiate either form differentiated multinucleated myotubes or give rise to quiescent, undifferentiated "reserve cells" that share several characteristics with muscle satellite cells. The mechanism of determination of reserve cells is poorly understood. We find that the expression level of the metalloprotease disintegrin ADAM12 is much higher in proliferating C2C12 myoblasts and in reserve cells than in myotubes. Inhibition of ADAM12 expression in differentiating C2C12 cultures by small interfering RNA is accompanied by lower expression levels of both quiescence markers (retinoblastoma-related protein p130 and cell cycle inhibitor p27) and differentiation markers (myogenin and integrin alpha7A isoform). Overexpression of ADAM12 in C2C12 cells under conditions that promote cell cycle progression leads to upregulation of p130 and p27, cell cycle arrest, and downregulation of MyoD. Thus, enhanced expression of ADAM12 induces a quiescence-like phenotype and does not stimulate differentiation. We also show that the region extending from the disintegrin to the transmembrane domain of ADAM12 and containing cell adhesion activity as well as the cytoplasmic domain of ADAM12 are required for ADAM12-mediated cell cycle arrest, while the metalloprotease domain is not essential. Our results suggest that ADAM12-mediated adhesion and/or signaling may play a role in determination of the pool of reserve cells during myoblast differentiation.

ADAM Proteins↗
PubMed2003

[Epidemiological study on group infection of Angiostrongylus cantonensis in Changle City].

OBJECTIVE: To make etiological and epidemiological investigation on the infection of Angiostrongylus cantonensis in 8 pupils in Changle City. METHODS: 1. CSF of patients was examined with the conventional method to detect pathogens and eosinophiles. 2. The fecal samples of wild rodents were collected from the spot and examined microscopically to discover the first stage larvae of A. cantonensis. 3. Snails (Pila gigas) were collected in the spot. The smashed head tissue was examined for the third stage larvae of A. cantonensis. 4. The patient's clinical symptoms and physical signs were recorded with an emphasis on central nervous system. RESULTS: 1. Two larvae of the third stage of A. cantonensis were found in CSF of one patient. Eosinophiles occupied 68% of the cell number in average (ranged from 47% to 83%) in CSF of the 8 patients. 2. The infection rate of the first stage larvae of A. cantonensis was 39.3% (44/112) in feces of the rodents. 3. The infection rate of the third stage larvae of A. cantonensis was 40.0% (82/205) in the snails. 4. Major clinical manifestations in the 8 patients included: severe headache(8/8), dizziness(8/8), nausea(8/8), vomiting(8/8), lethargy(7/8), lower limb hypodynamia(7/8). CONCLUSION: The confirmation of severe infection of A. cantonensis in 8 child patients demonstrated that a natural nidus of angiostrongyliasis is present in Chengle City.

Adolescent↗
PubMed2003

[Histo-morphological changes of eustachian tube of guinea pigs with effusion after being treated by pulmonary surfactant].

OBJECTIVE: To study the effect of pulmonary surfactant on otitis media with effusion in guinea pigs to find a new way to manage otitis media with effusion. METHODS: Nonviable heat-killed pneumococci (HKP) solution was inoculated into the middle ear cavity in guinea pigs via a transeardrum approach to set up a model of otitis media with effusion in guinea pigs. Seven days after being injected with pulmonary surfactant (PS) by transeardrum approach, ABR threshold and histomorphological changes of eustachian tube mucosa of guinea pigs were examined by light microscopy and scanning microscopy. RESULTS: Five days following inoculation of HKB serous effusion were present in the middle ear cavity of guinea pigs, but disappearance of light cone. Response (mean +/- s) threshold raised from (14.0 +/- 3.1) dB to (45.0 +/- 5.7) dB. The eustachian tube mucosa was thickened and lined eosin-stained structureless matter over mucosa, while cilia of eustachian tube mucosa irregularly arranged. Seven days after being treated by PS, serous effusion of tympanum was reduced or disappeared, and response threshold decreased from (45.0 +/- 5.7) dB to (23.5 +/- 6.3) dB. There was significantly difference between them (P < 0.001). Eustachian tube mucosa was thinned, Cilia of eustachian tube mucosa regularly arranged to the nasopharynx. CONCLUSION: Pulmonary surfactant plays a important role in otitis media with effusion of guinea pigs.

Animals↗
PubMed2002

Intracellular processing of metalloprotease disintegrin ADAM12.

ADAM12 has been implicated in cell-cell interactions in myogenesis and cancer, but the structure of the mature form of ADAM12 is not known, and its localization on the cell surface has been questioned. In this report, we show that full-length ADAM12 is N-glycosylated in the endoplasmic reticulum (ER) and proteolytically processed in the trans-Golgi network to an approximately 90-kDa form. The approximately 90-kDa form, which lacks the prodomain, was the predominant form present at the cell surface. Replacement of Leu(73) in the putative alpha-helical region in the prodomain with proline resulted in retention of ADAM12 in the ER and a complete lack of its processing. However, deletion of the entire pro- and metalloprotease domains did not affect the processing and trafficking of ADAM12. In contrast, replacement of the cytoplasmic domain of ADAM12 with that of ADAM9 or adding a c-Myc tag at the C terminus led to a significant increase in transport of the protein to the cell surface. These results suggest that the cytoplasmic domain of ADAM12 plays an important role in regulating ADAM12 exit from the ER. We conclude that properly folded mouse ADAM12, after passing a rate-limiting step of exit from the ER, is processed in the secretory pathway and reaches the cell surface, where it can mediate adhesion-mediated signaling.

ADAM Proteins↗
PubMed2002

Differential expression of beta-galactoside alpha2,6 sialyltransferase and sialoglycans in normal and cirrhotic liver and hepatocellular carcinoma.

SUMMARY: Sialyltransferases sialylate plasma glycoproteins in hepatocytes and may (as hepatic key enzymes) constitute markers for liver diseases. We examined expression of the prevalent alpha2,6 sialyltransferase (ST6Gal I) and sialoglycans in normal liver, cirrhotic liver, and hepatocellular carcinoma (HCC) using a new ST6Gal I-specific mAb and recombinant fusion proteins of CD22 and sialoadhesin recognizing alpha2,6- or alpha2,3-sialylated glycans in immunohistology and flow cytometry. In normal and cirrhotic liver, ST6Gal I and sialoglycans were localized in the Golgi region of hepatocytes surrounding the bile canaliculi and along the bile canaliculi, respectively. Sialoglycans were additionally recognized in Kupffer cells, bile ducts, endothelial cells, and oval cells. Well-differentiated and moderately differentiated HCC showed Golgi and diffuse cytoplasmic staining of ST6Gal I and sialoglycans, whereas the cytoplasmic staining for ST6Gal I and sialoglycans was decreased or even absent in poorly differentiated HCC. Detection of sialoglycans by the recombinant fusion proteins in Western blots of cell lysates derived from cell lines revealed two major double bands of sialoglycoproteins at 65 and 120 kDa for hepatocytes, three major bands at 54, 49, and 44 kDa for colonic epithelial cells, and one band at 60 kDa for endothelial cells. Our results describe the expression patterns of ST6Gal I and sialoglycans in various liver tissues and demonstrate an altered expression of these structures between benign and malignant hepatocellular lesions.

Antigens, CD↗
PubMed2002

[The mechanism and application of posttranscriptional gene silencing].

The purpose of this review is to confirm the reason resulted the gene silence and explore the countermeasure avoiding the gene silence in transgene plant. The method is to divide the gene silencing into transcriptional gene silencing(TGS) and posttranscriptional gene silencing(PTGS). Several models resulted PTGS were analyzed by RNA threshold model, ectopic pairing and aberrant RNA model and ds-RNA model. The results showed that it was important to decide the phenomena of restraining transgene silencing and the mechanism of PTGS. The strategies of identification of gene function and prevention of virus were presented by RNAi and gene silencing respectively, etc.

Animals↗
PubMedDate not supplied

Degradation behavior of poly(epsilon-caprolactone)-b-poly(ethylene glycol)-b-poly(epsilon-caprolactone) micelles in aqueous solution.

Poly(epsilon-caprolactone)-b-poly(ethylene glycol)-b-poly(epsilon-caprolactone) triblock copolymers were synthesized by the ring-opening polymerization of epsilon-caprolactone in the presence of hydroxyl-terminated poly(ethylene glycol) with different molecular weights, using stannous octoate catalyst. Micelles prepared by the precipitation method with these triblock copolymers exhibit a core-shell structure. The degradation behaviors of these core-shell micelles in aqueous solution were investigated by FT-IR, 1H NMR, GPC, DLS, TEM, and AFM. It was found that the degradation behavior of micelles in aqueous solution was quite different from that of bulk materials. The size of the micelles increased in the initial degradation stages and decreased gradually when the degradation period was extended. The caprolactone/ethylene oxide (CL/EO) ratio in micelles measured by NMR also shows an increase at the initial degradation stage and a decrease at later stages. The morphology of these micelles became more and more irregular during the degradation period. We explain the observed behavior by a two-stage degradation mechanism with interfacial erosion between the cores and the shells followed by core erosion.

Caproates↗