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2.
Poult Sci ; 97(3): 962-969, 2018 Mar 01.
Article in English | MEDLINE | ID: mdl-29365180

ABSTRACT

Vertical integration of the broiler industry allows producers to combine different biosecurity and sanitation practices, housing technologies, and feeding regimens to improve food safety. The purpose of this study was to investigate the prevalence of Staphylococcus aureus (S. aureus) and to characterize the antimicrobial-resistant isolates recovered from 7 different integrated broiler operation systems in Korea. Among 200 chicken meat samples, 94 were observed to be positive for S. aureus. However, the prevalence varied from 25.0 to 58.3% in chicken meats, indicating variation in S. aureus occurrence among the operations. Four methicillin-resistant S. aureus isolates (MRSA) were recovered from 3 different operations. A high proportion of the S. aureus isolates were resistant to penicillins (51.2%), tetracycline (38.8%), and ciprofloxacin (CIP; 33.9%). Especially, 3 different operations showed a high number of CIP resistance (45.5∼100%) and multidrug resistance (50.0∼100%). Among 41 CIP-resistant S. aureus isolates, 75.6% showed a double amino-acid exchange of both gyrA and parC, with CIP minimum inhibitory concentrations (MIC) of ≥32 µg/mL. Four MRSA isolates showed resistance to 5 or 7 classes of antimicrobial agents, exhibiting oxacillin, CIP, and enrofloxacin MIC ranges of 16 to 128, 32 to 64, and 8 to 128 µg/mL, respectively, and had double mutations of S84L/S80F in gyrA/parC. Our findings suggest that S. aureus with resistance to important antimicrobial compounds can now be found in association with integrated broiler operations, providing the data to support the development of a monitoring and prevention program in integrated operations.


Subject(s)
Animal Husbandry/methods , Anti-Bacterial Agents/pharmacology , Chickens , Drug Resistance, Bacterial , Food Microbiology , Meat/microbiology , Staphylococcus aureus/drug effects , Animals , Methicillin-Resistant Staphylococcus aureus/drug effects , Microbial Sensitivity Tests , Republic of Korea
3.
Asian J Androl ; 15(4): 503-7, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23708462

ABSTRACT

Several reports have promoted the root-derived Korean red ginseng (KRG; Panax ginseng) as alternative treatment for erectile dysfunction (ED), and ginsenosides are known to be the principal active ingredients of ginseng. Recent studies showed that ginseng berries produce more ginsenosides than KRG; thus, we investigated the ability of the Korean ginseng berry extract GB0710 to relax the penile corpus cavernosum smooth muscle (CCSM) in this study. As a comparative control, the results were compared to those obtained using KRG. In addition, possible mechanisms of action for GB0710 were investigated. While KRG and GB0710 both displayed dose-dependent relaxation effects on precontracted rabbit CCSM in vitro, GB0710 was shown to be more potent than KRG. The GB0710-induced relaxation could be partially reduced by removing the endothelium. In addition, pre-treatment with several nitric oxide (NO) inhibitors significantly inhibited the relaxation of muscle strips. Furthermore, administration of GB0710 increased intracavernosal pressure (ICP) in a rat in vivo model in both a dose- and duration-dependent manner. Intracellular NO production in human microvascular endothelial cells could be induced by GB0710 and inhibited by N(G)-monomethyl-L-arginine. In conclusion, GB0710 had a greater relaxation effect on rabbit CCSM than did KRG extract, and increased ICP in a rat model in both a dose- and a duration-dependent manner. This relaxing effect might be mediated by NO production.


Subject(s)
Endothelial Cells/drug effects , Fruit , Panax/chemistry , Penile Erection/drug effects , Plant Extracts/pharmacology , Animals , Dose-Response Relationship, Drug , Endothelial Cells/cytology , Enzyme Inhibitors/pharmacology , Human Umbilical Vein Endothelial Cells , Humans , In Vitro Techniques , Male , Muscle, Smooth/drug effects , Muscle, Smooth/physiology , Nitric Oxide/metabolism , Penile Erection/physiology , Plant Roots/chemistry , Rabbits , Rats , Rats, Sprague-Dawley , Republic of Korea , omega-N-Methylarginine/pharmacology
4.
Int J Impot Res ; 25(2): 45-50, 2013.
Article in English | MEDLINE | ID: mdl-23254461

ABSTRACT

Ginseng is beneficial for many aspects of human physiology, including sexual function. In this study, we have evaluated the efficacy and safety of an extract of ginseng berry, which has a ginsenoside profile distinct from other parts of the plant, on sexual function in men with erectile dysfunction. In all, 119 men with mild-to-moderate ED participated in a multicenter, randomized, double-blind, parallel, placebo-controlled clinical study. They were administered 4 tablets of either standardized Korean ginseng berry (SKGB, 350 mg ginseng berry extract per tablet), or placebo, daily, for 8 weeks. Efficacy was assessed with the International Index of Erectile Function (IIEF)-15 and premature ejaculation diagnostic tool (PEDT) at the end of the 4th and 8th week. We observed that the total and each of the individual domain scores of IIEF-15 increased from 40.95 ± 7.05 to 46.19 ± 12.69 significantly in the SKGB by the 8th week (P<0.05). The erectile function domain of IIEF changed slightly from 17.17 ± 2.57 to 18.59 ± 5.99 in the SKGB group by the 8th week (P<0.05). In addition, PEDT scores significantly improved from 9.14 ± 4.57 to 7.97 ± 4.4 and 7.53 ± 4.26 in the SKGB group after 4 and 8 weeks of treatment (P<0.05). Safety markers including hormone and lipid in the blood were assessed at the end of the 4th and 8th week and they remained unchanged. Oral administration of the SKGB extract improved all domains of sexual function. It can be used as an alternative medicine to improve sexual life in men with sexual dysfunction.


Subject(s)
Erectile Dysfunction/drug therapy , Panax/chemistry , Plant Extracts/therapeutic use , Adult , Aged , Double-Blind Method , Ejaculation/drug effects , Fruit/chemistry , Ginsenosides/administration & dosage , Humans , Male , Middle Aged , Patient Satisfaction , Penile Erection/drug effects , Phytotherapy , Placebos , Plant Extracts/administration & dosage , Severity of Illness Index , Treatment Outcome
5.
Skin Pharmacol Physiol ; 23(6): 283-9, 2010.
Article in English | MEDLINE | ID: mdl-20523107

ABSTRACT

BACKGROUND/AIMS: Dietary antioxidants exert a photoprotective effect against UV radiation. However, the mechanism underlying the beneficial effects on skin of orally administered antioxidant is not very clear. The present study aimed to investigate the UVB-induced total antioxidant capacity (TAC) perturbation both in skin and blood and to study the beneficial mechanism of action of dietary epigallocatechin-3-gallate (EGCG). METHOD: Female HWY/Slc hairless rats were exposed to UVB radiation for 4 weeks and skin and blood TAC were measured at weeks 0, 2, and 4. The correlation between skin and blood TAC was assessed using Pearson's correlation analysis. To investigate the effect of dietary EGCG, female HWY/Slc hairless rats were fed EGCG and exposed to UVB radiation. At the end of the 8-week experimental period, transepidermal water loss (TEWL) and epidermal thickness were measured to assess skin damage, and TAC was analyzed in both skin and blood. RESULTS: UVB radiation significantly decreased skin and blood TAC, and there was a significant correlation between skin and blood TAC. Dietary EGCG significantly prevented UVB-induced adverse effects on epidermal thickness and TEWL, and the UVB-induced decrease in TAC recovered in both skin and blood. CONCLUSION: These results demonstrate that there is a close relationship between skin and blood TAC and the beneficial effect of oral antioxidants on skin may possibly be mediated through significant enhancement of blood TAC.


Subject(s)
Antioxidants/administration & dosage , Antioxidants/metabolism , Catechin/analogs & derivatives , Diet , Skin/metabolism , Ultraviolet Rays/adverse effects , Animals , Blood/metabolism , Catechin/administration & dosage , Catechin/blood , Catechin/metabolism , Female , Radiation-Protective Agents/administration & dosage , Radiation-Protective Agents/metabolism , Rats , Rats, Hairless , Skin/drug effects , Skin/radiation effects , Water Loss, Insensible/drug effects
6.
Oncogene ; 28(26): 2476-84, 2009 Jul 02.
Article in English | MEDLINE | ID: mdl-19448665

ABSTRACT

Neuroblastoma, derived from neural crest progenitor cells, is the most common extracranial solid tumor of childhood. Astrocyte elevated gene-1 (AEG-1) is a primary mediator of tumor progression and metastasis in several human cancers. In this study, we investigated the potential contribution of AEG-1 in human neuroblastoma pathogenesis. AEG-1 expression was significantly elevated in neuroblastoma patient-derived samples and neuroblastoma cell lines as compared with normal peripheral nerve tissues, normal astrocytes and immortalized melanocytes. Knockdown of AEG-1 by small interfering RNA reduced the tumorigenic properties of highly aggressive neuroblastoma cells. Conversely, over-expression of AEG-1 enhanced proliferation and expression of the transformed state in less aggressive neuroblastoma cells through activation of the phosphatidylinositol 3-kinase-Akt-signaling pathway and stabilization of MYCN. These provocative results indicate that AEG-1 may play a crucial role in the pathogenesis of neuroblastoma and could represent a potential target for therapeutic intervention.


Subject(s)
Cell Adhesion Molecules/metabolism , Neuroblastoma/metabolism , Neuroblastoma/pathology , Animals , Astrocytes/metabolism , Cell Adhesion Molecules/deficiency , Cell Adhesion Molecules/genetics , Cell Line, Tumor , Cell Proliferation , Cell Transformation, Neoplastic , Fetus/cytology , Gene Expression Regulation, Neoplastic , Gene Knockdown Techniques , Humans , Melanocytes/metabolism , Membrane Proteins , Mice , N-Myc Proto-Oncogene Protein , Neuroblastoma/genetics , Nuclear Proteins/metabolism , Oncogene Proteins/metabolism , Peripheral Nerves/cytology , Peripheral Nerves/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , RNA-Binding Proteins , Signal Transduction
7.
Skin Pharmacol Physiol ; 22(3): 137-41, 2009.
Article in English | MEDLINE | ID: mdl-19212149

ABSTRACT

BACKGROUND/AIMS: Excessive exposure to UV radiation causes acute adverse effects like sunburn and photosensitivity reactions and is involved in the induction and development of skin cancer. It has been reported that antioxidants have photoprotective effects against solar UV radiation. We investigated the effect of oral epigallocatechin gallate (EGCG), a powerful antioxidant in green tea, on the minimal erythema dose (MED) and UV-induced skin damage. METHOD: Female HWY/Slc hairless rats were fed the normal diet supplemented with 1,500 ppm EGCG for 8 weeks; then, the MED was determined and visual scores and transepidermal water loss were assessed to evaluate the severity of UV-induced skin damage. RESULTS: At week 8 of the study, the use of dietary EGCG significantly increased MED. UV-radiation-induced sunburn severity and alterations in epidermal barrier function were also attenuated by the supplementation of EGCG. CONCLUSION: Regular intake of EGCG strengthens the skin's tolerance by increasing MED and thus prevents UV-induced perturbation of epidermal barrier function and skin damage. These results suggest that EGCG is a potent candidate for systemic photoprotection.


Subject(s)
Antioxidants/therapeutic use , Catechin/analogs & derivatives , Erythema/prevention & control , Radiation-Protective Agents/therapeutic use , Radiodermatitis/prevention & control , Ultraviolet Rays/adverse effects , Administration, Oral , Animals , Antioxidants/administration & dosage , Catechin/administration & dosage , Catechin/therapeutic use , Dose-Response Relationship, Radiation , Female , Radiation-Protective Agents/administration & dosage , Rats , Rats, Hairless , Tea , Water Loss, Insensible/physiology
8.
Transplant Proc ; 38(5): 1618-21, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16797369

ABSTRACT

The expression of human complement regulatory proteins (CRP) and H-transferase (HT) in porcine cells is one of the strategies for suppression of hyperacute rejection (HAR) of xenotransplants in human recipients. In this study, we investigated the inhibitory effect of combined expression of human complement regulators and HT on human serum-mediated cytolysis in porcine embryonic fibroblasts. For the combinated expression of human CRPs in transformed pig cells, cDNAs of human DAF, MCP, and CD59 were cloned into the same insertional plasmid under the control of pCMV IE and LTR. The double combination of CRPs, hDAF-hMCP, and hMCP-hCD59 survived over 50% in the presence of 50% human serum, compared to the control. Moreover, the cell viability was increased more than 65% and 80% in the combination of human DAF-CD59 and DAF-MCP-CD59, respectively. In addition, the combination of HT gene to hDAF-hCD59 vector increased the viability close to 80%, similar to the triple combination of CRPs. These observations suggest that the combined expression of human CRPs and HT in the same insertional vector may be more effective in protecting porcine cells from human complement-mediated cytolysis.


Subject(s)
Complement Inactivator Proteins/physiology , Complement System Proteins/physiology , Fibroblasts/physiology , Receptors, Complement/genetics , Animals , Animals, Genetically Modified , CD55 Antigens/genetics , CD59 Antigens/genetics , Cell Culture Techniques , Cell Survival , Fibroblasts/cytology , Genetic Vectors , Graft Rejection/prevention & control , Humans , Reverse Transcriptase Polymerase Chain Reaction , Swine , Transfection , Transplantation, Heterologous
9.
Mol Reprod Dev ; 71(3): 315-20, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15806556

ABSTRACT

Inefficiency in the production of cloned animals is most likely due to epigenetic reprogramming errors after somatic cell nuclear transfer (SCNT). In order to investigate whether nuclear reprogramming restores cellular age of donor cells after SCNT, we measured telomere length and telomerase activity in cloned pigs and cattle. In normal pigs and cattle, the mean telomere length was decreased with biological aging. In cloned or transgenic cloned piglets, the mean telomere length was elongated compared to nuclear donor fetal fibroblasts and age-matched normal piglets. In cloned cattle, no increases in mean telomere length were observed compared to nuclear donor adult fibroblasts. In terms of telomerase activity, significant activity was observed in nuclear donor cells and normal tissues from adult or new-born pigs and cattle, with relatively higher activity in the porcine tissues compared to the bovine tissues. Cloned calves and piglets showed the same level of telomerase activity as their respective donor cells. In addition, no difference in telomerase activity was observed between normal and transgenic cloned piglets. However, increased telomerase activity was observed in porcine SCNT blastocysts compared to nuclear donor cells and in vitro fertilization (IVF)-derived blastocysts, suggesting that the elongation of telomere lengths observed in cloned piglets could be due to the presence of higher telomerase activity in SCNT blastocysts. In conclusion, gathering from the comparative studies with cattle, we were able to demonstrate that telomere length in cloned piglets was rebuilt or elongated with the use of cultured donor fetal fibroblasts.


Subject(s)
Blastocyst/metabolism , Cloning, Organism , Telomerase/metabolism , Telomere/metabolism , Animals , Cattle , Gene Expression Regulation, Developmental/physiology , Swine , Up-Regulation/physiology
10.
DNA Cell Biol ; 20(2): 75-80, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11244564

ABSTRACT

Hepatitis B virus X (HBx) protein is known as an oncogenic transactivator, E2F1 as a positive regulator of the cell cycle, and pRb as a tumor suppressor. Here, we investigated the functional interactions of these proteins on the human Rb promoter. Interestingly, HBx transactivated the Rb promoter cooperatively with E2F1 in HepG2 cells but not in HeLa cells, in which the functions of p53 and pRb are inactive. Combinatorial cotransfection analyses in HepG2 cells showed that HBx overcame the inhibition of E2F1 activity by pRb but not that by p53. Domain analysis showed that aa 47-70 and aa 117-133 of HBx are important for this effect. These results suggest that HBx could inhibit the pRb tumor suppressor and increase E2F1 activity. Our data support the oncogenic potential of HBx, which may cause HBV-infected cells to grow continuously in the development of hepatocellular carcinoma.


Subject(s)
Carrier Proteins , Cell Cycle Proteins , DNA-Binding Proteins , Genes, Retinoblastoma , Hepatitis B virus/physiology , Promoter Regions, Genetic , Retinoblastoma Protein/physiology , Trans-Activators/physiology , Transcription Factors/antagonists & inhibitors , Transcription Factors/metabolism , E2F Transcription Factors , E2F1 Transcription Factor , Gene Expression Regulation, Neoplastic , Gene Expression Regulation, Viral , HeLa Cells , Humans , Peptide Fragments/physiology , Retinoblastoma Protein/antagonists & inhibitors , Retinoblastoma Protein/genetics , Retinoblastoma-Binding Protein 1 , Transcription Factor DP1 , Transcription Factors/physiology , Transfection , Viral Regulatory and Accessory Proteins
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