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7 protocols using testosterone

1

Glucose and Hormone Assay Protocol

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Blood glucose was estimated by glucose oxidase method using glucometer [26 (link)].
Plasma insulin, cortisol, testosterone, oestrogen (Calbiotech Inc., 1935 Cordell Ct., El Cajon, CA 92020) and glucagon (Bioassay Technology Laboratory, Yangpu Dist, Shanghai, China) were assayed spectrophotometrically (Beckman Coulter DTX 880 Multimode Detector) following the kit manufacturers’ procedure.
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2

Serum Hormone Quantification by ELISA

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Commercially available enzyme-linked immunosorbent assay (ELISA) kits were used to determine the serum concentration of leptin (Crystal Chem), T4 (Calbiotech), testosterone (Calbiotech), corticosterone (Arbor Assays), GH (Millipore), IGF-1 (R&D Systems) and prolactin (Sigma).
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Hormone Levels Quantification Protocol

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Commercially available ELISA kits were used to determine the serum concentration of leptin (Crystal Chem), T4 (Calbiotech), testosterone (Calbiotech), insulin (Crystal Chem), and corticosterone (Arbor Assays).
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4

Comprehensive Blood Analysis Protocol

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Hematocrit concentrations were analyzed in duplicate in whole blood using microcapillary and microcentrifugation (CritSpin, Westwood, MA, USA) techniques. Whole blood hemoglobin was analyzed in duplicate using an automated analyzer (HemoCue, Cypress, CA, USA). Plasma volume shifts were calculated using the formula established by Dill and Costill (1974). The coefficient of variation for hematocrit was 0.87% and was 0.65% for hemoglobin.
Serum concentrations of testosterone, cortisol, and myoglobin and plasma concentrations of BDNF, IL‐6 (High Sensitivity), and CRP, were obtained via commercially available enzyme‐linked immunosorbent assay (testosterone, cortisol, myoglobin: Calbiotech, Spring Valley, CA, USA; BDNF, High‐Sensitivity IL‐6, CRP: R&D Systems, Minneapolis, MN, USA) per manufacturer's instructions. All samples for a particular assay were thawed once and analyzed in duplicate by the same technician using a BioTek Eon spectrophotometer (BioTek Instruments, Inc., Winooski, VT, USA). Intra‐assay coefficients of variation for each assay were: 8.15% for testosterone; 9.21% for cortisol; 7.52% for myoglobin; 7.57% for BDNF; 5.50% for IL‐6; 3.36% for CRP. Interplate coefficients of variation for each assay were: 12.77% for testosterone; 4.85% for cortisol; 15.10% for myoglobin; 17.96% for BDNF; 5.92% for IL‐6; 6.03% for CRP.
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5

Biochemical Analyte Measurements in Plasma

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Blood glucose was estimated by glucose oxidase method using glucometer (26).
Plasma insulin, cortisol, testosterone, oestrogen (Calbiotech Inc., 1935 Cordell Ct., El Cajon, CA 92020) and glucagon (Bioassay Technology Laboratory, Yangpu Dist, Shanghai, China) were assayed spectrophotometrically (Beckman Coulter DTX 880 Multimode Detector) following the kit manufacturers' procedure.
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6

Endocrine Biomarkers Quantification

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Serum concentrations of estradiol, testosterone, insulin (Calbiotech, Spring Valley, CA, USA) and corticosterone (Demeditec diagnostics GmbH, Germany) were estimated using ELISA kits and procedures provided by the respective manufacturer.
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7

Prostate Biomarkers in BPH Patients

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27 BPH patients who were admitted in urology ward for transurethral resection of prostate surgery were recruited in the study. Subjects with prostate cancer and other medical co morbidities were excluded from the study. Written informed consent was obtained from all the subjects prior to the study. This study was approved by institute advisory committee and ethics committee. 5 ml of fasting venous blood samples were collected from the subjects and used for the analysis of PSA, Testosterone and Estrogen (Calbiotech Inc., Spring Valley, California) by using ELISA.
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