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Biomedical subjects

J Sun

Publications and source records attributed to J Sun.

At least 649 records · Page 36Linked to original sources

[Treatment with Western and Chinese medicine for retinal pigmentary degeneration].

The report presents 45 cases of retinal pigmentary degeneration treated by Western and Chinese medicine. Of them, 14 cases (31.11%) got significant therapeutical effectiveness; 18 cases (40%) favorite and 6 cases (13.33%) were improved. The general curative rate was 84.44%. After follow-up for 1 to 5 years, the vision and visual field in all the cases were improved to a certain extent. We used the dose of Chinese herbal medicine, the decoction of retinal pigmentary degeneration, in the treatment. The result showed it is a very beneficial method for retinal pigmentary degeneration.

Adolescent↗

[The changes in the summating potential and morphology in the cochlea of guinea pigs with anoxia].

The dynamic changes in the CAP, SP and EP in the scale media were examined with single micropipet during anoxia and reventilation with oxygen. Also, the morphologic changes in the IHC, OHC and synapse were observed in this experiment. It was found that the amplitude of the SP and EP values declined with alteration in polarity of these value. The changes in polarity and amplitude of the SP followed the changes of CAP threshold induced by anoxia. The histologic examinations revealed no evidence of acetylcholinesterase (AChE) alteration in the synapse and no succinic dehydrogenase (SDH) changes in IHC appeared. However, the activity of SDH in the OHC decreased. The results suggest that the polarity and amplitude of SP were influenced passively by the changes of EP value. In addition, the changes of SP polarity from positive to negative during anoxia is due to the loss of modulation process of OHC to IHC, while the SP polarity from negative to positive during the supply of oxygen is caused by regain of the modulation process of OHC.

Acetylcholinesterase↗

The optimization of technological condition in the fermentation process of glutamate by pattern recognition method.

The technological condition in the fermentation process of fermentation glutamate (such as pH value, temperature, ventilation rate, etc.) were optimized by computerized pattern recognition method. The visible optimum region may be found based on the mapping from the multi-dimensional pattern space into a plane. It is then transformed along the reciprocal direction into the original data space using Monte Carlo simulation, so the orientation of optimization and the best combination of all parameters can be determined. A new mathematical model is being proposed based on the experimental evidence in production. The transfer ratio of glucose to glutamic acid, the production capacity and the glutamic acid concentration increase 2.9%, 1.45% and 2.65% respectively by operating this optimization method. The method has been widely extended to factories and has granted in decreasing the expense of raw materials and that of the production cost.

Fermentation↗

Effects of Sr-hydroxyapatite microcrystal on cultured cell.

Strontium-hydroxyapatite microcrystals (Sr-HAp sol) were produced by a wet method at room temperature with ultrasonic irradiation and were applied to MC3T3-E1, ROS, and L cells for periods of 2, 4, and 6 days in vitro. The effect on cell growth, the variation of LDH and Ca contents in the media, and attachment between cell and microcrystal were investigated. Sintered Sr-HAp and HAp sol were used as controls. A slight inhibitory effect of Sr-HAp sol on cell growth was found. The degree of inhibition was nearly the same as HAp sol. However, it was stronger than sintered Sr-HAp. The contents of LDH in the media increased with the degree of cell inhibition, and the contents of Ca in the media decreased from the initial stage of cell-sol contact. A good attachment of Sr-HAp sol to cultured cells was seen by phase-contrast microscopy and SEM.

Animals↗

Characterization of polyketide ketoreductase gene (MPKR) from midecamycin-producing strain (Streptomyces mycarofaciens 1748).

This paper presents the results about the expression of the polyketide ketoreductase gene from midecamycin-producing strain (S. mycarofaciens 1748), gene localization and nucleotide sequences analysis. A BamHI-BamHI 4.0 kg fragment isolated from a genomic library of midecamycin-producing strains containing the actIII homologous DNA was inserted into E. coli-Streptomyces shuttle vector pWHM3. A recombinant plasmid pCB4 was obtained and introduced into a 2-hydroxyaklavinone producer S. galilaeus ATCC 31671 that was a polyketide ketoreductase gene deficient mutant. The transformant produced aklavinone according to TLC and HPLC analyses. The BamHI-BamHI 4.0-kb fragment was inserted into pWHM3 in the reverted orientation with pCB4 and a recombinant plasmid pCBR4 was obtained. Introduction pCBR4 into S. galilaeus ATCC 31671 also resulted in the production of aklavinone. Thus we demonstrated that this gene encoded a polyketide ketoreductase which results in deoxygenation of 2-hydroxyaklavinone in C-2 position and that this gene has its own promoter. Restriction map analysis of pCB4 indicated that there were no sites for EcoRI and HindIII, but there were sites for BssHII, SalI, SphI and XhoI on the cloned gene fragment. The polyketide ketoreductase gene was located on a BssHII-BamHI 1.3-kb fragment from Southern hybridization result, using actIII gene as a probe, and that was confirmed by gene expression in S. galilaeus ATCC 31671. The nucleotide sequence analysis showed that the BssHII-BamHI 1.3-kb fragment contained an open reading frame (ORF). The protein coding region was assumed to start with an ATG start codon, end at an TAG stop codon. There was a 5nt (GGAGG) SD sequence at the upstream of start codon. A presumptive promoter consisted of 7 nt AACCGGA at the -10 region and 5 nt TTCGA at the -35 region. The deduced amino acid sequences of MPKR gene consisted of 261 aa residues. Its amino acid were compared with actIII gene coding protein sequences. The similarity was 77.4% and the identity was 66.7%.

Amino Acid Sequence↗

Further characterization of endometrial integrins during the menstrual cycle and in pregnancy.

OBJECTIVE: To profile the changes in integrin expression in cycling and pregnant endometrium. DESIGN: Immunohistochemistry was performed on endometrium from proliferative, early, and midsecretory phase and early pregnancy using a blinded panel of monoclonal antibodies directed against integrins. Closer examination of the cycle-dependent integrins was performed in 112 patients throughout the cycle and from the first trimester of pregnancy. SETTING: An academic teaching hospital. PATIENTS: Ovulatory women or women undergoing pregnancy termination. MAIN OUTCOME MEASURE: Staining intensity of each antibody in epithelial or stromal cells. RESULTS: Certain integrins were present constitutively throughout the menstrual cycle whereas others were expressed only during the luteal phase. Four integrins increased in the decidua of pregnancy. The timing of expression of the two cycle-dependent integrins (alpha 4 beta 1 and alpha v beta 3) framed the putative window of implantation and suggests a role in establishment of uterine receptivity. CONCLUSIONS: Our findings confirm the patterns of endometrial integrins and suggest important roles for integrins in the process of implantation and decidualization.

Antibodies, Monoclonal↗

[Synaptonemal complex analysis of 13/17 Robertsonian translocation in the domestic pig].

G and C-banding study of the chromosomes of several male pigs, indicate that all of these pigs carry rob(13;17). The karyotype is 2n = 37, XY, rob (13;17). In this paper, silverstained Synaptonemal Complexes (SCs) in surface-spread pachytene nuclei from these pigs are analysed by electron microscope. The result is as follows: Robertsonian translocation metacentrics rob (13;17) paired with homologous acrocentrics (13,17), forming a trivalent. All trivalents are in a cis configuration and there is delayed pairing in the trivalent. We measured every part of trivalent in the different stage of prophase (based on the morphology of XY-bivalent). It is shown that accompanying with rob(13;17) formation there has been a deletion in the proximal part of 13, 17 translocation chromosome. In the process of synapsis, the length adjustment phenomenon in the trivalent occurred: a. There is nonhomologous synapsis between the two short arms of the acrocentrics (13;17). The length of short SC varied. b. The position of the short SC, which is on the long SC(homologous synapsis of rob(13; 17) and 13, 17) moved, from one-fourth of long SC to one-tenth of it, near the end of 17 arm. These phenomenon is the result of a gradual length adjustment of lateral elements of 13,17 to the lateral element of the rob (13;17). We has discussed the mechanism of the trivalent synaptic adjustment, and it's important use to control the chiasmata and disjunction of the chromosomes.

Animals↗

[The effects of hypertonic and balanced saline solutions on burn shock resuscitation in burned rats].

Hypertonic saline solution (HS) has been used effectively to treat different kinds of shock. In this experiment, all rats are inflicted with a full-thickness burn of 20% BSA, and they are divided into three groups. Group I, control; group II, resuscitated with balanced saline solution; group III, with HS. All animals are sacrificed at 24 hours postburn to determine blood viscosity (BV) and tissue water content (TWC), as well as to observe the microcirculation in kidney with electronmicroscopy. We find that the TWC increased significantly in group II (P < 0.05), while BV decreased, especially in group III (P < 0.01). The electronmicroscopic observation indicates that: In group I, there are capillary dilatation, red cell aggregation, endothelium edema, and appearance of many gaps between endothelium. In group II, the blood flows easily and smoothly. In group III, the improvement of microcirculation is not significant and the blood vessel is filled with microthromboli. The results show that HS can improve systemic circulation, but not microcirculation.

Animals↗

Resonance Raman and EPR spectroscopic studies on heme-heme oxygenase complexes.

The binding of ferrous and ferric hemes and manganese(II)- and manganese(III)-substituted hemes to heme oxygenase has been investigated by optical absorption, resonance Raman, and EPR spectroscopy. The results are consistent with the presence of a six-coordinate heme moiety ligated to an essential histidine ligand and a water molecule. The latter ionizes with a pKa approximately 8.0 to give a mixture of high-spin and low-spin six-coordinate hydroxo adducts. Addition of excess cyanide converts the heme to a hexacoordinate low-spin species. The resonance Raman spectrum of the ferrous heme-heme oxygenase complex and that of the Mn(II)protoporphyrin-heme oxygenase complex shows bands at 216 and 212 cm-1, respectively, that are assigned to the metal-histidine stretching mode. The EPR spectrum of the oxidized heme-heme oxygenase complex has a strongly axial signal with g parallel of approximately 6 and g perpendicular approximately 2. 14NO and 15NO adducts of ferrous heme-heme oxygenase exhibit EPR hyperfine splittings of approximately 20 and approximately 25 Gauss, respectively. In addition, both nitrosyl complexes show additional superhyperfine splittings of approximately 7 Gauss from spin-spin interaction with the proximal histidine nitrogen. The heme environment in the heme-heme oxygenase enzyme-substrate complex has spectroscopic properties similar to those of the heme in myoglobin. Hence, there is neither a strongly electron-donating fifth (proximal) ligand nor an electron-withdrawing network on the distal side of the heme moiety comparable to that for cytochromes P-450 and peroxidases. This observation has profound implications about the nature of the oxygen-activating process in the heme-->biliverdin reaction that are discussed in this paper.

Cations, Divalent↗

Cloning and molecular characterization of a human intracellular serine proteinase inhibitor.

We describe a cDNA encoding a serine proteinase inhibitor present in placental tissue and the cytosolic fraction of K562 cells. On the basis of its interaction with thrombin, through which it was discovered, the inhibitor has been operationally named the placental thrombin inhibitor (PTI). Amino acid sequence comparisons suggest that its reactive center is located at Arg-341 and Cys-342, that it lacks a classical N-terminal signal sequence, and that it has the highest degree of similarity to intracellular serine proteinase inhibitors (serpins), such as the human monocyte/neutrophil elastase inhibitor and the equine leukocyte elastase inhibitor. PTI also resembles these inhibitors in that it contains oxidation-sensitive residues adjacent to the reactive site. The PTI cDNA was expressed in rabbit reticulocyte lysate and in COS-7 cells and a 42-kDa protein was produced. Recombinant PTI formed a 67-kDa complex when incubated with thrombin. The ability of native PTI to bind thrombin was destroyed by incubation with iodoacetamide. Analysis of human tissue mRNA indicated that PTI is expressed widely with the highest levels in cardiac and skeletal muscle and placenta. We conclude that PTI is a member of an emerging class of intracellular serpins.

Amino Acid Sequence↗

Association of annexin V with mitochondria.

Annexin V is an intracellular protein recently shown to be localized to nucleoli and cytosol. In this study we show that cytosolic annexin V is associated with mitochondria. To assess the nature of the annexin V-mitochondrial interaction, an annexin V binding activity was partially purified from placental cytosol by annexin V-affinity chromatography. Five polypeptides in the eluate appeared to be associated with annexin V, with a predominant species of 27 kDa. Antibodies to the 27 kDa polypeptide recognised mitochondria but not nucleoli. We conclude that annexin V interacts with a 27 kDa mitochondrial polypeptide that is possibly part of a larger complex.

Annexin A5↗

Effects of annexin V on the activity of the anticoagulant proteins C and S.

The effects of annexin V on the anticoagulant activity of activated protein C (APC) and protein S were examined. Although annexin V did not influence the amidolytic potential of APC, it inhibited both APC and protein S function in a factor Va inactivation assay. Competition experiments demonstrated that annexin V inhibits protein S binding to phospholipid vesicles in a dose-dependent manner. These results demonstrate that annexin V effectively interferes with the anticoagulant arm of the hemostatic system.

Annexin A5↗

Interaction of annexin V and platelets: effects on platelet function and protein S binding.

Intact annexin V but not its fragments bound specifically to platelets in the presence of calcium. Maximal binding observed was 0.87 pmole annexin V per 10(8) platelets with an apparent dissociation constant of 2.13 x 10(-11) M. This represents approximately 5000 binding sites per platelet. Platelet stimulation by thrombin increased the binding of annexin V by 40-fold. Addition of phospholipid vesicles or treatment with phospholipase C inhibited annexin V binding to platelets, suggesting that phospholipid is the binding site for annexin V and that phosphatidylcholine forms at least part of this site. Binding of annexin V did not cause platelet aggregation and did not affect thrombin or collagen induced aggregation. However annexin V significantly inhibited the binding of protein S to the platelet surface.

Annexin A5↗

Promoter activity of human renin 5'-flanking DNA sequences is activated by the pituitary-specific transcription factor Pit-1.

Although the renal juxtaglomerular cell is the source of circulating renin, the renin gene is also expressed at a number of extrarenal sites including lactotrope cells of human and ovine pituitaries. In the present study, we demonstrate that GC cells, a pituitary lactotrope precursor cell line, efficiently express transiently transfected hybrid genes containing human renin 5'-flanking DNA sequences -148/+11. Gel mobility shift competition analyses show that a highly conserved sequence in human and rodent renin 5'-flanking DNAs (human coordinates: -80/-58) binds a nuclear factor from GC cells, most likely the pituitary-specific factor Pit-1. Deletional and mutational analyses demonstrate that this site is a major determinant of renin promoter activity in GC cells. Transfection of a Pit-1 expression construct into HeLa cells, where activity of the human renin promoter is low, stimulates expression of cotransfected renin-luciferase constructs. Moreover, activation of the human renin promoter by co-expression of Pit-1 is dependent on an intact Pit-1 site. Taken together, these data strongly suggest that Pit-1 activates pituitary renin gene expression. This finding raises the possibility that member(s) of the POU family of transcription factors, of which Pit-1 is an archetypal member, may direct renin expression in other tissues, including the kidney.

Animals↗

Influences of neurotrophins on mammalian motoneurons in vivo.

Several recently reported investigations have shown that a member of the neurotrophin family of neuronal growth factors, brain-derived neurotrophic factor (BDNF), supports motoneurons in vitro and rescues motoneurons from naturally occurring and axotomy-induced cell death (Oppenheim et al., 1992b; Sendtner et al., 1992b; Yan et al., 1992; Koliatsos et al., 1993; Henderson et al., 1993). In the current study, we have explored the issue of whether BDNF and other neurotrophins act to regulate motoneuron survival during development and asked whether synthesis of motoneuron transmitter enzymes is also regulated. We first examined whether spinal motoneurons in newborn animals could retrogradely transport iodinated neurotrophins from their targets in a specific, receptor-mediated manner. We found that motoneurons readily transported NGF, BDNF, and neurotrophin-3 (NT-3). The retrograde transport of one factor could be completely or largely blocked by excess of unlabeled homologous factor, but only partially blocked by excess of unlabeled heterologous factors. Since previous studies have shown that these three neurotrophins bind to the low-affinity NGF receptor, p75NGFR, with similar affinity, our data suggest that the retrograde transport of neurotrophins by motoneurons may be mediated by additional components, such as the trk family of proto-oncogenes. Consistent with this hypothesis, we demonstrate here that motoneurons express mRNA for two members of the trk family, trkB and trkC. Furthermore, both trkB and trkC were expressed by E13, consistent with a role for BDNF and NT-3 in regulating important developmental events involving motoneurons such as naturally occurring cell death. In order to determine which members of the neurotrophin family influence motoneuron survival and to assess the generality of their effects, we evaluated the abilities of NGF, BDNF, and NT-3 to save both spinal and cranial motoneurons after neonatal axotomy. Locally applied BDNF saved 40-70% of motoneurons which would ordinarily die after axotomy in lumbar and cranial motor pools, depending on the treatment protocol employed. NT-3 also exhibited some ability to rescue motoneurons and saved 20-25% of motoneurons which would die in the absence of treatment. Finally, we asked whether neurotrophins could influence synthesis of transmitter enzymes by motoneurons as well as their survival after axotomy. Locally applied BDNF and NT-3 could partially prevent the decrease of protein contents in L4 and L5 ventral roots which normally follows sciatic nerve transection. However, treatment with these neurotrophins did not prevent the decrease in choline acetyltransferase (ChAT) activity in L4 and L5 ventral roots which results from this procedure.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

A single gene change can extend yeast life span: the role of Ras in cellular senescence.

The budding yeast Saccharomyces cerevisiae has a limited life span (reproductive capacity), which is measured by the number of times an individual cell divides. There is evidence for the involvement of a senescence factor that affects cell cycle traversal in older yeast cells. Distinct alterations in the abundance of a handful of transcripts have been identified during the life span of this organism, and the genes that specify these mRNAs have been cloned. This raises the question whether the activity of one or more genes can alter the yeast life span. Indeed, the controlled expression of the transforming gene of Harvey murine sarcoma virus (v-Ha-ras) was found to extend the life span nearly two-fold. The normal homologs of this oncogene, RAS1 and RAS2, play a central role in the integration of cell growth and the cell cycle in yeast. Expression of v-Ha-ras appears to impinge on this integration. We suggest that it is the relative levels of the senescence factor and the Ras protein that determine whether a cell ceases to divide and senesces. We liken the senescence factor to the product of an anti-oncogene or tumor suppressor gene that neutralizes Ras.

Cell Cycle↗

Coincident indices of exons and introns.

In this paper, the coincident index, proposed by W. F. Friedman in cryptology, is made use of in DNA sequence analysis and exon prediction. The coincident index of exons exceeds that of introns by many times, and is mainly affected by window length, which is correlated negatively with the coincident index. An optimal exon prediction scheme was obtained by experimental analysis with an orthogonal table. Besides exons, many other special sites such as tandem repeats can be identified by using the coincident index approach. The application of this approach to the ARV-2 (AIDS associated retrovirus 2) genome found three new possible coding regions and some unusual base composition regions which are probably related to definite biological functions.

Base Composition↗

Effect of thiazide diuretics against neurally mediated contraction of guinea pig airways. Contribution of carbonic anhydrase.

The effect of thiazide diuretics on neurally and agonist-induced contractile responses of guinea pig airways in vitro were investigated. Tracheal or bronchial strips were suspended in organ baths and isometric tension recorded. Chlorothiazide (CTZ, 10(-4) to 3 x 10(-3) M), hydrochlorothiazide (HCTZ, 10(-3) M), and dichlorphenamide (DCPM, 10(-3) M) significantly potentiated contraction of tracheal strips induced by electrical field stimulation (EFS). They also increased acetylcholine (ACh)- but not carbachol-induced tracheal contraction. In the presence of atropine and propranolol, on the other hand, CTZ and DCPM but not HCTZ significantly inhibited EFS-induced contraction in bronchial strips. We determined whether carbonic anhydrase inhibition could mimic the effects of CTZ and DCPM. Acetazolamide (ATZ), an inhibitor of carbonic anhydrase, had no effect on either EFS- or ACh-induced contraction in tracheal strips but significantly inhibited nonadrenergic, noncholinergic (NANC) contractile responses induced by EFS in bronchial strips. CTZ, DCPM, and ATZ did not affect substance P-induced contractile responses in the bronchi. We conclude that CTZ, DCPM, and ATZ attenuate NANC neurally mediated bronchial contraction by preventing the release of contractile neuropeptides from sensory nerve endings. This effect may occur through inhibition of carbonic anhydrase activity. In addition, thiazide diuretics potentiate contractile responses to ACh in the trachea, probably through inhibition of acetylcholinesterase activity.

Acetylcholine↗