• 제목/요약/키워드: blood biochemistry

검색결과 633건 처리시간 0.064초

산란계의 혈액화학치 측정에 의한 지방간 출혈 증후군의 조기 진단 (Early Diagnosis of Fatty Liver-Hemorrhagic Syndrome using Blood Biochemistry in Commercial Layers)

  • 소현희;전은옥;변성환;모인필
    • 한국가금학회지
    • /
    • 제36권2호
    • /
    • pp.165-175
    • /
    • 2009
  • 국내 실용 산란계 농장에서 FLHS 병력을 지닌 계군과 정상계군에 대한 특정 혈액화학치를 비교 측정하여 다음과 같은 결과를 얻었다. FLHS 계군의 간의 지방 함량과 vacuolation score가 Non-FLHS 계군보다 높게 나타났으며, FLHS를 확인하는데 간의 지방 함량과 조직 병리학적 소견을 평가하는 것이 유의성이 있음을 확인할 수 있었다(p<0.05). 또한, FLHS 계군과 Non-FLHS계군이 실험군으로서 명확하게 구분이 되었다. Non-FLHS와 FLHS 계군의 다섯 가지의 혈액화학치를 측정한 결과, cholesterol, AST, LDH의 평균 수치가 Non- FLHS 계군보다 FLHS 계군이 높았으며, FLHS를 확인하는데 cholesterol, AST, LDH가 유의성 있는 항목임을 알 수 있었다(p<0.05). FLHS 계군은 Non-FLHS 계군보다 CK는 높지 않으면서, AST가 높게 나타났으며, FLHS를 진단하기 위해 AST를 측정할 때, CK를 비교 항목으로 이용하는 것이 유용하다는 것을 확인할 수 있었다. Serum AST는 케이지에서 사육되는 산란계에서 FLHS 발생시 현저하게 상승되는 항목으로, FLHS 계군 중에는 250 IU/L 이상을 보이는 개체가 있었으나, Non-FLHS 계군에는 250 IU/L 이상을 보이는 개체가 없었다. MINITAB을 이용하여 판별 분석을 실시한 결과, AST의 판별 추정 계수가 cholesterol이나 LDH보다 큰 수치를 나타내어, AST가 FLHS의 판별에 더 큰 의미를 부여하는 유용한 항목임을 다시 확인할 수 있었다.

Endotoxins of Enteric Pathogens Are Chemotactic Factors for Human Neutrophils

  • Islam, Laila N.;Nabi, A.H.M. Nurun;Ahmed, K. Mokim;Sultana, Novera
    • BMB Reports
    • /
    • 제35권5호
    • /
    • pp.482-487
    • /
    • 2002
  • Early activation of human peripheral blood polymorphonuclear neutrophils is characterized by their morphological changes from spherical to polarized shapes. The endotoxins from enteric pathogens (S. dysenteriae type 1, V. cholerae Inaba 569B, S. typhimurium, and K. pneumoniae) were assessed by their ability to induce morphological polarization of the neutrophils as measures of early activation. Phagocytic activity, adhesion, chemokinetic locomotion, and nitroblue tetrazolium (NBT) dye-reduction ability measured the later activation of the cells. Neutrophils showed distinct morphological polarization in suspension over a wide range of concentrations of these endotoxins when were compared with those that were induced by the standard chemotactic factor, N-formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP). It was discovered that all of the endotoxins induced locomotor responses in neutrophils in suspension that were dose- and time-dependent. The optimum concentration for the endotoxins of S. dysenteriae, V. cholerae, and K. pneumoniae was 1 mg/ml in which 71, 69, and 66% of the neutrophils were polarized. However, the S. typhimurium dose was 2 mg/ml in which 50% of the cells responded. Neutrophils that were stimulated with endotoxins also showed increased random locomotion (p<0.005) through cellulose nitrate filters, but an enhanced adhesion of the cells to glass surfaces (p<0.03). These are important functions of these cells to reach and phagocytose damaged cells, as well as invading microorganisms. Interestingly, the endotoxins had a highly-significant inhibitory effect upon the proportions of neutrophils phagocytosing opsonized yeast (p<0.01) with a small number of yeast that were engulfed by the cells (p<0.02). Further, endotoxin-treated cells showed an enhanced ability to reduce NBT dye (p<0.03). Therefore, we concluded that endotoxins of enteric pathogens are neutrophil chemotactic factors.

Role of Hyperinsulinemia in Increased Risk of Prostate Cancer: A Case Control Study from Kathmandu Valley

  • Pandeya, Dipendra Raj;Mittal, Ankush;Sathian, Brijesh;Bhatta, Bibek
    • Asian Pacific Journal of Cancer Prevention
    • /
    • 제15권2호
    • /
    • pp.1031-1033
    • /
    • 2014
  • Aim: To investigate the effect of hyperglycemia and hyperinsulinemia on prostate cancer risk. Materials and Methods: This hospital based study was carried out using data retrieved from the register maintained in the Department of Biochemistry of a tertiary care hospital of Kathmandu, Nepal between $31^{st}$ December, 2011 and $31^{st}$ October, 2013. The variables collected were age, serum cholesterol, serum calcium, PSA, fasting blood glucose, serum insulin. Analysis was performed by descriptive statistics and testing of hypothesis using Excel 2003, R 2.8.0, Statistical Package for the Social Sciences (SPSS) for Windows Version 16.0 (SPSS Inc; Chicago, IL, USA) and the EPI Info 3.5.1 Windows Version. Results: Of the total 125 subjects enrolled in our present study, 25 cases were of PCa and 100 were healthy controls. The mean value of fasting plasma glucose was 95.5 mg/dl in cases of prostatic carcinoma and the mean value of fasting plasma insulin was $5.78{\mu}U/ml$ (p value: 0.0001*). The fasting insulin levels ${\mu}U/ml$ were categorized into the different ranges starting from ${\leq}2.75$, >2.75 to ${\leq}4.10$, >4.10 to ${\leq}6.10$, > $6.10{\mu}U/ml$. The maximum number of cases of prostatic carcinoma of fasting insulin levels falls in range of > $6.10{\mu}U/ml$. The highest insulin levels (> $6.10{\mu}U/ml$) were seen to be associated with an 2.55 fold risk of prostatic carcinoma when compared with fasting insulin levels of (< $2.75{\mu}U/ml$). Conclusions: Elevated fasting levels of serum insulin appear to be associated with a higher risk of prostate cancer.

Intrauterine diabetic milieu instigates dysregulated adipocytokines production in F1 offspring

  • Tawfik, Shady H.;Haiba, Maha M.;Saad, Mohamed I.;Abdelkhalek, Taha M.;Hanafi, Mervat Y.;Kamel, Maher A.
    • Journal of Animal Science and Technology
    • /
    • 제59권1호
    • /
    • pp.1.1-1.11
    • /
    • 2017
  • Background: Intrauterine environment plays a pivotal role in the origin of fatal diseases such as the metabolic syndrome. Diabetes is associated with low-grade inflammatory state and dysregulated adipokines production. The aim of this study is to investigate the effect of maternal diabetes on adipocytokines (adiponectin, leptin and TNF-${\alpha}$) production in F1 offspring in rats. Methods: The offspring groups were as follows: F1 offspring of control mothers under control diet (CD) (CF1-CD), F1 offspring of control mothers under high caloric diet (HCD) (CF1-HCD), F1 offspring of diabetic mothers under CD (DF1-CD), and F1 offspring of diabetic mothers under HCD (DF1-HCD). Every 5 weeks post-natal, 10 pups of each subgroup were culled to obtain blood samples for biochemical analysis. Results: The results indicate that DF1-CD and DF1-HCD groups exhibited hyperinsulinemia, dyslipidemia, insulin resistance and impaired glucose homeostasis compared to CF1-CD (p > 0.05). DF1-CD and DF1-HCD groups had high hepatic and muscular depositions of TGs. The significant elevated NEFA level only appeared in offspring of diabetic mothers that was fed HCD. DF1-CD and DF1-HCD groups demonstrated low serum levels of adiponectin, high levels of leptin, and elevated levels of TNF-${\alpha}$ compared to CF1-CD (p > 0.05). These results reveal the disturbed metabolic lipid profile of offspring of diabetic mothers and could guide further characterization of the mechanisms involved. Conclusion: Dysregulated adipocytokines production could be a possible mechanism for the transgenerational transmittance of diabetes, especially following a postnatal diabetogenic environment. Moreover, the exacerbating effects of postnatal HCD on NEFA in rats might be prone to adipcytokine dysregulation. Furthermore, dysregulation of serum adipokines is a prevalent consequence of maternal diabetes and could guide further investigations to predict the development of metabolic disturbances.

프로테오믹스 기술을 통한 쥐의 신장 피질에서 알도스테론(Aldosterone)에 의해 조절되는 단백질 동정 (Proteome-based Identification of Proteins Regulated by Aldosterone in Rat Kidney Cortex)

  • 송미나;전홍배;최효정;권태환;백문창
    • 약학회지
    • /
    • 제54권3호
    • /
    • pp.180-186
    • /
    • 2010
  • Aldosterone, mineralocorticoid hormone, has important functions related to the regulation of blood pressure and balance of fluids and electrolytes in the distal region of the nephron. By genomic and non-genomic action of aldosterone, the physiological kidney functions are modulated. However, many of them except several kind of sodium channel have not been identified and analyzed yet. In this study, proteomic technologies with two-dimensional gel electrophoresis (2-DE) gel using aldosterone rat model were applied to analyze and identify the aldosterone dependently expressed proteins in rat kidney cortex. As a result, the established aldosterone rat model exhibited the normal physiological responses to aldosterone and modulated proteins were identified, which included 15 increased and 3 decreased proteins on 2-DE analysis. Among them, 11 proteins were identified as changed proteins by LC-MS/MS analysis. These proteins identified as aldosterone induced proteins were involved in several cellular pathways such as cytoskeleton remodeling, energy metabolism, amino acid metabolism, and chaperone process. In conclusion, our data could provide the insights into the new mechanism underlying regulation of kidney functions by aldosterone.

Genetic structure of apical membrane antigen-1 in Plasmodium falciparum isolates from Pakistan

  • Komal Zaib;Asifullah Khan;Muhammad Umair Khan;Ibrar Ullah;Tuan Cuong Vo;Jung-Mi Kang;Huong Giang Le;Byoung-Kuk Na;Sahib Gul Afridi
    • Parasites, Hosts and Diseases
    • /
    • 제62권3호
    • /
    • pp.302-312
    • /
    • 2024
  • Plasmodium falciparum apical membrane antigen-1 (PfAMA-1) is a major candidate for the blood-stage malaria vaccine. Genetic polymorphisms of global pfama-1suggest that the genetic diversity of the gene can disturb effective vaccine development targeting this antigen. This study was conducted to explore the genetic diversity and gene structure of pfama-1 among P. falciparum isolates collected in the Khyber Pakhtunkhwa (KP) province of Pakistan. A total of 19 full-length pfama-1 sequences were obtained from KP-Pakistan P. falciparum isolates, and genetic polymorphism and natural selection were investigated. KP-Pakistan pfama-1 exhibited genetic diversity, wherein 58 amino acid changes were identified, most of which were located in ectodomains, and domains I, II, and III. The amino acid changes commonly found in the ectodomain of global pfama-1 were also detected in KP-Pakistan pfama-1. Interestingly, 13 novel amino acid changes not reported in the global population were identified in KP-Pakistan pfama-1. KP-Pakistan pfama-1 shared similar levels of genetic diversity with global pfama-1. Evidence of natural selection and recombination events were also detected in KP-Pakistan pfama-1.

제주 흑우에서 다배란 처리 후 호르몬 수준과 혈액 생화학치의 변화 (Changes of Hormonal Level and Blood Biochemistry Following Superovulation Treatments of Jeju Black Cow)

  • 이태훈;강승률;김희석;강민수;윤영민;이주명;강태영
    • 한국수정란이식학회지
    • /
    • 제21권3호
    • /
    • pp.225-231
    • /
    • 2006
  • 본 연구는 제주도의 흑우에서 다배란을 유기한 후 발정기 동안 혈중 호르몬의 농도 검사, 혈액 생화학 검사, 체내 수정란 회수율 등을 관찰하였다. FSH를 4일간 8회 50 mg씩 주사하여 다배란을 유기하였다. 성호르몬의 측정은 radioimmunoassay (RIA)법으로 측정하였으며 혈액 생화학치는 자동혈청 분석기로 측정하였다. 인공 수정 후 7일에 수정란을 비외과적 방법으로 회수하였다. 본 연구의 결과는 다음과 같았다. 1. 혈중 호르몬의 농도를 측정한 결과 progesterone농도는 day -11에 $7.2{\pm}3.8ng/ml$ 이었으며 day -2에 급격히 감소하여 day 0에는 $0.2{\pm}0.1ng/ml$로 최저치를 유지하다가 day 2 후 상승하였다. Estradiol의 농도는 day -11에 $10.6{\pm}4.3pg/ml$였으며 day 0에는 $15.0{\pm}2.1pg/ml$ 로 최고치를 기록했다. 2. 다배란처리 후 발정 주기 동안의 AST, ALT, BUN, creatine, cholesterol, albumin 및 total protein등 혈액 생화학치의 변화를 측정한 결과 각 혈액 생화학치의 변화는 정상 소의 정상 범위 내 있었으며 유의적 차이는 없었다. 3. 공란우 12두에서 총 62개의 수정란을 회수하였다. 이중 이식 가능한 수정란은 37개(59.7%)였다. 본 연구의 결과로 제주흑우에서 다배란을 유도한 후 발정기 중 호르몬과 혈액생화학치의 변화양상을 알 수 있었다.

천연기념물 한국 산양의 혈액 및 혈액 화학적 정상표준범위 (Hematologic and biochemical reference intervals for natural monument Korean goral (Naemorhedus caudatus))

  • 안상진;최영진;김종택
    • 한국동물위생학회지
    • /
    • 제40권2호
    • /
    • pp.155-159
    • /
    • 2017
  • Korean goral (Neamorhedus caudatus) is registered as a natural monument number 217 by South Korea Cultural Heritage Administration. It is also recognized as the endangered species I by Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). In this study, blood samples of Korean goral were collected to make reference intervals. Blood sampling was conducted on 19 numbers of Korean gorals (ten females, nine males), which were reared in Korean Goral Restoration Center. For total samples, the reference intervals of hematological parameters were: white blood cell $7.69{\sim}10.87K/{\mu}{\Lambda}$; hematocrit 36.73~46.18%; red blood cell $10.72{\sim}12.86K/{\mu}{\Lambda}$; hemoglobin 12.79~15.14 g/dL; mean corpuscular volume 33.15~36.75 fL; mean corpuscular hemoglobin 11.53~12.23 pg; mean corpuscular hemoglobin concentration 32.64-35.91 g/dL and red blood cell distribution width 39.2~43.46%. For total samples of each parameters, the following results were obtained for serum biochemistry: glucose 111.81~153.77 mg/dL; blood urea nitrogen 22.35~28.91 mg/dL; creatine 1.22~1.84 mg/dL; phosphate 4.57~6 mg/dL; calcium 8.7~9.1 mg/dL; total protein 6.53~6.92 g/dL; albumin 3.1~3.48 g/dL; globulin 3.26~3.62 g/dL; alanine aminotransferase 56.7~158.56 U/L; aspartate aminotransferase 230.35~473.06 U/L; alkaline phosphatase 178.06~332.47 U/L; gamma-glutamyl transpeptidase 131.6-~181.24 U/L; total bilirubin 1.47~2.12 mg/dL; cholesterol 46.48~71.52 mg/dL; amylase 16.3~26.03 U/L; sodium 150.43~153.88 mmol/L; potassium 3.98~4.6 mmol/L and chlorine 109.48~113.26 mmol/L. The ranges of values were similar campared to previous studies except in the case of RDW value, which showed higher range than the RDW value of a previous study. The reference intervals from this study will be useful data for treatment and management of gorals.

Role of the surface loop on the structure and biological activity of angiogenin

  • Jang, Seung-Hwan;Song, Hyang-Do;Kang, Dong-Ku;Chang, Soo-Ik;Kim, Min-Kyung;Cho, Kwang-Hwi;Scherga, Harold A.;Shin, Hang-Cheol
    • BMB Reports
    • /
    • 제42권12호
    • /
    • pp.829-833
    • /
    • 2009
  • Angiogenin is a member of the ribonuclease superfamily that induces the formation of new blood vessels. It has been suggested that the surface loop of angiogenin defined by residues 59-71 plays a special role in angiogenic function (1); however, the mechanism of action is not clearly defined. To elucidate the role of the surface loop on the structure, function and stability of angiogenin, three surface loop mutants were produced in which 14 amino acids in the surface loop of RNase A were substituted for the 13 amino acids in the corresponding loop of angiogenin. The structure, stability and biological functions of the mutants were then investigated using biophysical and biological approaches. Even though the substitutions did not influence the overall structure of angiogenin, they affected the stability and angiogenic function of angiogenin, indicating that the surface loop of angiogenin plays a significant role in maintaining the stability and angiogenic function of angiogenin.

Development and Immunochemical Properties of Two Monoclonal Antibodies Specific to Human Chorionic Gonadotropin

  • Kim, You-Hee;Koh, Kwan-Sam
    • BMB Reports
    • /
    • 제32권5호
    • /
    • pp.474-479
    • /
    • 1999
  • Using a hybridoma technique, spleen cells of Balb/c mice immunized with human chorionic gonadotropin (hCG) were fused with NS-1 mouse myeloma cells. Two hybrid cell lines, clones KS-8 and KS-19, secreting monoclonal antibodies to hCG, were isolated. KS-8 and KS-19 belong to the immunoglobulin $G_1$ subclass. With the aid of a double-antibody radioimmunoassay, it was established that the KS-8 monoclonal antibody recognizes an immunodeterminant of the $\beta$-subunit of hCG, whereas the KS-19 monoclonal antibody recognizes an epitope present on the $\alpha$-subunit of hCG. The KS-8 monoclonal antibody specifically reacts with human chorionic gonadotropin and shows cross-reactivity of less than 0.3% to other related human glycoprotein hormones. On the other hand, using a hemagglutination test based on antibody-induced agglutination of sheep red blood cells coated with hCG, It was shown that only the KS-19 monoclonal antibody was capable of inducing a positive reaction, although both monoclonal antibodies had similar binding capacity to the coated cells. The results from the dual screening procedures demonstrate that KS-8 and KS-19 monoclonal antibodies show high sensitivity in two different assays, and are hence useful for the qualitative and quantitative determination of hCG by both radioimmunoassay and hemagglutination inhibition tests.

  • PDF