dht Search Results


94
Elabscience Biotechnology dht
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
Dht, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Novus Biologicals nbp2 67999
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
Nbp2 67999, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
steraloids inc 5α dihydrotestosterone
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
5α Dihydrotestosterone, supplied by steraloids inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
Cerilliant Corporation 5a dihydrotestosterone dht 290 44 cerilliant
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
5a Dihydrotestosterone Dht 290 44 Cerilliant, supplied by Cerilliant Corporation, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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94
Cusabio rat specific dht
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
Rat Specific Dht, supplied by Cusabio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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93
Cayman Chemical dht
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
Dht, supplied by Cayman Chemical, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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88
Cusabio canine dihydrotestosterone dht elisan kit
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
Canine Dihydrotestosterone Dht Elisan Kit, supplied by Cusabio, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Eagle Biosciences elisa kit
Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. <t>D-G</t> <t>ELISA</t> analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of <t>DHT</t> level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001
Elisa Kit, supplied by Eagle Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dht  (Cusabio)
92
Cusabio dht
Figure 2. FNS‑loaded microspheres effectively prevent 5α‑reductase activity in a testosterone‑induced androgenic alopecia mouse model. (A) Schematic diagram of the study protocol. The mice were administered with the test compounds orally or subcutaneously for 8 weeks. (B) Images of the dorsal skin at 8 weeks. Individual data were obtained using enzyme‑linked immunosorbent assays for <t>(C)</t> <t>testosterone</t> and (D) <t>DHT</t> in serum. The DHT levels decreased 4 weeks after orally‑applied FNS and FNS‑loaded microspheres administration. All data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 and **P<0.01, vs. microspheres‑treated group. FNS, finasteride; TP, testosterone propionate; DHT, dihydrotestosterone.
Dht, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
Cusabio human dihydrotestosterone elisa kit
Figure 2. Permeability and adhesion study on CaCo-2 cells. In (A), Cell viability is measured by using the MTT test; in (B), TEER Value using EVOM3; in (C), SCFA analysis is conducted using an <t>ELISA</t> kit; in (D), butyric acid analysis is carried out using an ELISA kit; in (E) the analysis of aggregation activity and in (F) the analysis of hydrophobicity activity. Data are mean ± SD of five independent experiments performed in triplicates compared to control values (0% line). In (A,C–F), * p < 0.05 vs. control; ** p < 0.05 vs. single agents. In (B), p < 0.05 vs. control; ** p < 0.05 vs. single agents.
Human Dihydrotestosterone Elisa Kit, supplied by Cusabio, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Valiant Co Ltd rabbit antiserum
Figure 2. Permeability and adhesion study on CaCo-2 cells. In (A), Cell viability is measured by using the MTT test; in (B), TEER Value using EVOM3; in (C), SCFA analysis is conducted using an <t>ELISA</t> kit; in (D), butyric acid analysis is carried out using an ELISA kit; in (E) the analysis of aggregation activity and in (F) the analysis of hydrophobicity activity. Data are mean ± SD of five independent experiments performed in triplicates compared to control values (0% line). In (A,C–F), * p < 0.05 vs. control; ** p < 0.05 vs. single agents. In (B), p < 0.05 vs. control; ** p < 0.05 vs. single agents.
Rabbit Antiserum, supplied by Valiant Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
FUJIFILM dht (dehydrotestosterone)
Figure 2. Permeability and adhesion study on CaCo-2 cells. In (A), Cell viability is measured by using the MTT test; in (B), TEER Value using EVOM3; in (C), SCFA analysis is conducted using an <t>ELISA</t> kit; in (D), butyric acid analysis is carried out using an ELISA kit; in (E) the analysis of aggregation activity and in (F) the analysis of hydrophobicity activity. Data are mean ± SD of five independent experiments performed in triplicates compared to control values (0% line). In (A,C–F), * p < 0.05 vs. control; ** p < 0.05 vs. single agents. In (B), p < 0.05 vs. control; ** p < 0.05 vs. single agents.
Dht (Dehydrotestosterone), supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. D-G ELISA analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of DHT level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001

Journal: Cell Communication and Signaling : CCS

Article Title: Dual deficiency of melatonin and dihydrotestosterone promotes stromal cell damage and mediates prostatitis via the cGAS-STING pathway in sleep-deprived mice

doi: 10.1186/s12964-024-01554-5

Figure Lengend Snippet: Characteristics and proteomic analysis of prostate in mice after 3 weeks of SD. A Photos of prostate and corresponding sizes (prostate index) analysis. B HE staining showing the typical pathological changes of prostatitis. C Quantification of urinary frequency by urine spots assay. D-G ELISA analysis of cytokines in serum, including IL-6, TNF-α, PGE2 and IFN-β. H-K ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, PGE2 and IFN-β. Proteomic analysis of control and SD mice including ( L ) KEGG pathway enrichment, ( M ) hierarchical clustering heatmap, and ( N ) volcano plot of differentially expressed proteins. O Proteomic analysis showing the underlying mechanism of prostatitis induction. P Analysis of MT level in serum after 3 weeks of SD. Q-R Analysis of DHT level in serum and prostate tissue after 3 weeks of SD. S Schematic hypothesis of the cGAS-STING pathway activation by the dual deficiency of MT and DHT for inducing inflammatory microenvironment in prostate. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the Student’s t test ( A , C , D - K , and P - R ). ns, no significance, ** P < 0.01, and *** P < 0.001

Article Snippet: Cytokine levels in mouse plasma and prostate tissue homogenate samples were detected using ELISA kits for MT (E-EL-M0788c, Elabscience, Wuhan, China), DHT (E-EL-0031c, Elabscience, Wuhan, China), E2 (E-OSEL-M0008, Elabscience, Wuhan, China), T (E-OSEL-M0003, Elabscience, Wuhan, China), GnRH (E-EL-0071c, Elabscience, Wuhan, China), LH (E-EL-M3053, Elabscience, Wuhan, China), IFN-β (EK2236-96, MULTISCIENCES, Hangzhou, China), TNF-ɑ (EK282/4–96, MULTISCIENCES, Hangzhou, China), IL-6 (EK206/3–96, MULTISCIENCES, Hangzhou, China), and PGE2 (EK8103/2–96, MULTISCIENCES, Hangzhou, China).

Techniques: Staining, Enzyme-linked Immunosorbent Assay, Control, Activation Assay

Induction of cGAS-STING pathway-mediated prostatitis by co-inhibiting MT and DHT in normal mice. A Schematic illustration of treatment by MT inhibitor (4-P-PDOT) and DHT inhibitor (finasteride) in normal mice for 3 weeks. 4-P-PDOT and finasteride were used to establish the mice model with dual deficient MT and DHT, which was applied to verify the relationship between dual deficient MT and DHT and prostatitis in SD mice. B-C Photos of prostate and corresponding sizes (prostate index) analysis. D The level of DHT in prostate of mice treated by finasteride. E Changes of tactile allodynia by Von Frey filaments. F HE staining showing the changes of prostate in mice after 4-P-PDOT and finasteride treatment. Scale bar, 100 μm. G-H The indexes of oxidative stress in prostate, including MDA and SOD. I-K ELISA analysis of cytokines in serum, including IL-6, TNF-α, and PGE2. L-N ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, and PGE2. O-P Immunohistochemical staining of p-TBK1 and p-IRF3. Scale bar, 100 μm. Q-R The corresponding average optical density (AOD) of immunohistochemistry for p-TBK1 and p-IRF3. S-T The changes of IFN-β levels in serum and prostate tissue. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the one-way ANOVA ( C-E , G-N , and Q-T ). ns, no significance, and *** P < 0.001

Journal: Cell Communication and Signaling : CCS

Article Title: Dual deficiency of melatonin and dihydrotestosterone promotes stromal cell damage and mediates prostatitis via the cGAS-STING pathway in sleep-deprived mice

doi: 10.1186/s12964-024-01554-5

Figure Lengend Snippet: Induction of cGAS-STING pathway-mediated prostatitis by co-inhibiting MT and DHT in normal mice. A Schematic illustration of treatment by MT inhibitor (4-P-PDOT) and DHT inhibitor (finasteride) in normal mice for 3 weeks. 4-P-PDOT and finasteride were used to establish the mice model with dual deficient MT and DHT, which was applied to verify the relationship between dual deficient MT and DHT and prostatitis in SD mice. B-C Photos of prostate and corresponding sizes (prostate index) analysis. D The level of DHT in prostate of mice treated by finasteride. E Changes of tactile allodynia by Von Frey filaments. F HE staining showing the changes of prostate in mice after 4-P-PDOT and finasteride treatment. Scale bar, 100 μm. G-H The indexes of oxidative stress in prostate, including MDA and SOD. I-K ELISA analysis of cytokines in serum, including IL-6, TNF-α, and PGE2. L-N ELISA analysis of cytokines in prostate tissue, including IL-6, TNF-α, and PGE2. O-P Immunohistochemical staining of p-TBK1 and p-IRF3. Scale bar, 100 μm. Q-R The corresponding average optical density (AOD) of immunohistochemistry for p-TBK1 and p-IRF3. S-T The changes of IFN-β levels in serum and prostate tissue. Data were presented as means ± SEM ( n = 5). Statistical significance was calculated using the one-way ANOVA ( C-E , G-N , and Q-T ). ns, no significance, and *** P < 0.001

Article Snippet: Cytokine levels in mouse plasma and prostate tissue homogenate samples were detected using ELISA kits for MT (E-EL-M0788c, Elabscience, Wuhan, China), DHT (E-EL-0031c, Elabscience, Wuhan, China), E2 (E-OSEL-M0008, Elabscience, Wuhan, China), T (E-OSEL-M0003, Elabscience, Wuhan, China), GnRH (E-EL-0071c, Elabscience, Wuhan, China), LH (E-EL-M3053, Elabscience, Wuhan, China), IFN-β (EK2236-96, MULTISCIENCES, Hangzhou, China), TNF-ɑ (EK282/4–96, MULTISCIENCES, Hangzhou, China), IL-6 (EK206/3–96, MULTISCIENCES, Hangzhou, China), and PGE2 (EK8103/2–96, MULTISCIENCES, Hangzhou, China).

Techniques: Staining, Enzyme-linked Immunosorbent Assay, Immunohistochemical staining, Immunohistochemistry

Progression of prostatitis in sleep-deprived mice after sleep recovery. A Schematic illustration of sleep recovery for different time (1 to 3 weeks) in SD mice. B Analysis of MT level in serum in SD mice after 3 weeks of sleep-recovery (R1, R2, and R3). C Analysis of DHT level in prostate tissue after 3 weeks of sleep-recovery. D The prostate sizes (prostate index) analysis. E-G ELISA analysis of cytokines in prostate, including IL-6, TNF-α, and PGE2. H-I The concentration of IFN-β in serum and prostate tissue. J HE staining showing the changes of prostate in SD mice after 1 week of sleep-recovery. Scale bar, 100 μm. K The corresponding inflammation score analysis of prostate in HE staining. L Evaluation of tactile allodynia by Von Frey filaments in mice. M-N Western blot and corresponding analysis of the essential proteins of cGAS-STING pathway in prostate of mice after 1 week of sleep-recovery. O Schematic illustration of sleep re-deprivation for different time (1, 3 and 7 days) in mice. P HE staining revealing the changes of prostate in sleep-recovery mice after sleep re-deprivation (R-SD) for different periods (1, 3, and 7 days). Scale bar, 100 μm. Data were presented as means ± SEM ( n ≥ 5). Statistical significance was calculated using the one-way ANOVA ( B - I , K , L , and N ). ns, no significance, * P < 0.05, ** P < 0.01, and *** P < 0.001

Journal: Cell Communication and Signaling : CCS

Article Title: Dual deficiency of melatonin and dihydrotestosterone promotes stromal cell damage and mediates prostatitis via the cGAS-STING pathway in sleep-deprived mice

doi: 10.1186/s12964-024-01554-5

Figure Lengend Snippet: Progression of prostatitis in sleep-deprived mice after sleep recovery. A Schematic illustration of sleep recovery for different time (1 to 3 weeks) in SD mice. B Analysis of MT level in serum in SD mice after 3 weeks of sleep-recovery (R1, R2, and R3). C Analysis of DHT level in prostate tissue after 3 weeks of sleep-recovery. D The prostate sizes (prostate index) analysis. E-G ELISA analysis of cytokines in prostate, including IL-6, TNF-α, and PGE2. H-I The concentration of IFN-β in serum and prostate tissue. J HE staining showing the changes of prostate in SD mice after 1 week of sleep-recovery. Scale bar, 100 μm. K The corresponding inflammation score analysis of prostate in HE staining. L Evaluation of tactile allodynia by Von Frey filaments in mice. M-N Western blot and corresponding analysis of the essential proteins of cGAS-STING pathway in prostate of mice after 1 week of sleep-recovery. O Schematic illustration of sleep re-deprivation for different time (1, 3 and 7 days) in mice. P HE staining revealing the changes of prostate in sleep-recovery mice after sleep re-deprivation (R-SD) for different periods (1, 3, and 7 days). Scale bar, 100 μm. Data were presented as means ± SEM ( n ≥ 5). Statistical significance was calculated using the one-way ANOVA ( B - I , K , L , and N ). ns, no significance, * P < 0.05, ** P < 0.01, and *** P < 0.001

Article Snippet: Cytokine levels in mouse plasma and prostate tissue homogenate samples were detected using ELISA kits for MT (E-EL-M0788c, Elabscience, Wuhan, China), DHT (E-EL-0031c, Elabscience, Wuhan, China), E2 (E-OSEL-M0008, Elabscience, Wuhan, China), T (E-OSEL-M0003, Elabscience, Wuhan, China), GnRH (E-EL-0071c, Elabscience, Wuhan, China), LH (E-EL-M3053, Elabscience, Wuhan, China), IFN-β (EK2236-96, MULTISCIENCES, Hangzhou, China), TNF-ɑ (EK282/4–96, MULTISCIENCES, Hangzhou, China), IL-6 (EK206/3–96, MULTISCIENCES, Hangzhou, China), and PGE2 (EK8103/2–96, MULTISCIENCES, Hangzhou, China).

Techniques: Enzyme-linked Immunosorbent Assay, Concentration Assay, Staining, Western Blot

Figure 2. FNS‑loaded microspheres effectively prevent 5α‑reductase activity in a testosterone‑induced androgenic alopecia mouse model. (A) Schematic diagram of the study protocol. The mice were administered with the test compounds orally or subcutaneously for 8 weeks. (B) Images of the dorsal skin at 8 weeks. Individual data were obtained using enzyme‑linked immunosorbent assays for (C) testosterone and (D) DHT in serum. The DHT levels decreased 4 weeks after orally‑applied FNS and FNS‑loaded microspheres administration. All data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 and **P<0.01, vs. microspheres‑treated group. FNS, finasteride; TP, testosterone propionate; DHT, dihydrotestosterone.

Journal: International journal of molecular medicine

Article Title: Development of finasteride polymer microspheres for systemic application in androgenic alopecia.

doi: 10.3892/ijmm.2019.4149

Figure Lengend Snippet: Figure 2. FNS‑loaded microspheres effectively prevent 5α‑reductase activity in a testosterone‑induced androgenic alopecia mouse model. (A) Schematic diagram of the study protocol. The mice were administered with the test compounds orally or subcutaneously for 8 weeks. (B) Images of the dorsal skin at 8 weeks. Individual data were obtained using enzyme‑linked immunosorbent assays for (C) testosterone and (D) DHT in serum. The DHT levels decreased 4 weeks after orally‑applied FNS and FNS‑loaded microspheres administration. All data are presented as the mean ± standard error of the mean from three independent experiments. *P<0.05 and **P<0.01, vs. microspheres‑treated group. FNS, finasteride; TP, testosterone propionate; DHT, dihydrotestosterone.

Article Snippet: Serum testosterone (cat. no. CSB‐E05101m) and DHT (cat. no. CSB‐E07880m) were measured via enzyme linked immunosorbent assays (ELISA; Cusabio, Wuhan, China).

Techniques: Activity Assay

Figure 2. Permeability and adhesion study on CaCo-2 cells. In (A), Cell viability is measured by using the MTT test; in (B), TEER Value using EVOM3; in (C), SCFA analysis is conducted using an ELISA kit; in (D), butyric acid analysis is carried out using an ELISA kit; in (E) the analysis of aggregation activity and in (F) the analysis of hydrophobicity activity. Data are mean ± SD of five independent experiments performed in triplicates compared to control values (0% line). In (A,C–F), * p < 0.05 vs. control; ** p < 0.05 vs. single agents. In (B), p < 0.05 vs. control; ** p < 0.05 vs. single agents.

Journal: Foods (Basel, Switzerland)

Article Title: Analysis of the Beneficial Effects of Probiotics on the Gut-Prostate Axis Using Prostatic Co-Culture Model.

doi: 10.3390/foods13223647

Figure Lengend Snippet: Figure 2. Permeability and adhesion study on CaCo-2 cells. In (A), Cell viability is measured by using the MTT test; in (B), TEER Value using EVOM3; in (C), SCFA analysis is conducted using an ELISA kit; in (D), butyric acid analysis is carried out using an ELISA kit; in (E) the analysis of aggregation activity and in (F) the analysis of hydrophobicity activity. Data are mean ± SD of five independent experiments performed in triplicates compared to control values (0% line). In (A,C–F), * p < 0.05 vs. control; ** p < 0.05 vs. single agents. In (B), p < 0.05 vs. control; ** p < 0.05 vs. single agents.

Article Snippet: According to the manufacturer, a Human Dihydrotestosterone ELISA Kit (Cusabio, Houston, TX, USA) was used to measure DHT in co-culture prostatic supernatants [43].

Techniques: Permeability, Enzyme-linked Immunosorbent Assay, Activity Assay, Control

Figure 3. Integrity analysis. In (A), the analysis of claudin-1 measured by ELISA test; in (B), the analysis of ZO-1 by ELISA test; in (C), the analysis of occludin-1 by ELISA kit. Data are mean ± SD of five independent experiments performed in triplicates vs. control values (0% line) and * p < 0.05 vs. control; ** p < 0.05 vs. single agents.

Journal: Foods (Basel, Switzerland)

Article Title: Analysis of the Beneficial Effects of Probiotics on the Gut-Prostate Axis Using Prostatic Co-Culture Model.

doi: 10.3390/foods13223647

Figure Lengend Snippet: Figure 3. Integrity analysis. In (A), the analysis of claudin-1 measured by ELISA test; in (B), the analysis of ZO-1 by ELISA test; in (C), the analysis of occludin-1 by ELISA kit. Data are mean ± SD of five independent experiments performed in triplicates vs. control values (0% line) and * p < 0.05 vs. control; ** p < 0.05 vs. single agents.

Article Snippet: According to the manufacturer, a Human Dihydrotestosterone ELISA Kit (Cusabio, Houston, TX, USA) was used to measure DHT in co-culture prostatic supernatants [43].

Techniques: Enzyme-linked Immunosorbent Assay, Control

Figure 4. Analysis of oxidative stress and inflammation. All of the following results are derived from the ELISA kit: (A) ROS generation; (B) SOD levels; (C) TNF-α production; (D) IL-6 production; and (E) IL-10 production. The mean ± SD of five separate studies conducted in triplicate is shown, along with * p < 0.05 vs. control, ** p < 0.05 vs. single drugs, and # p < 0.05 vs. DHT, in comparison to control values (0% line).

Journal: Foods (Basel, Switzerland)

Article Title: Analysis of the Beneficial Effects of Probiotics on the Gut-Prostate Axis Using Prostatic Co-Culture Model.

doi: 10.3390/foods13223647

Figure Lengend Snippet: Figure 4. Analysis of oxidative stress and inflammation. All of the following results are derived from the ELISA kit: (A) ROS generation; (B) SOD levels; (C) TNF-α production; (D) IL-6 production; and (E) IL-10 production. The mean ± SD of five separate studies conducted in triplicate is shown, along with * p < 0.05 vs. control, ** p < 0.05 vs. single drugs, and # p < 0.05 vs. DHT, in comparison to control values (0% line).

Article Snippet: According to the manufacturer, a Human Dihydrotestosterone ELISA Kit (Cusabio, Houston, TX, USA) was used to measure DHT in co-culture prostatic supernatants [43].

Techniques: Derivative Assay, Enzyme-linked Immunosorbent Assay, Control, Comparison

Figure 5. Mechanism analyses for prostate hyperplasia. Testosterone levels (A), 5α-reductase levels (B), DHT levels (C), AR levels (D), and PSA levels (E) are all derived from the ELISA kit. Values are mean ± SD from five independent tests in triplicates compared to control values (0% line). * p < 0.05 vs. control; ** p < 0.05 vs. single agents; # p < 0.05 vs. DHT.

Journal: Foods (Basel, Switzerland)

Article Title: Analysis of the Beneficial Effects of Probiotics on the Gut-Prostate Axis Using Prostatic Co-Culture Model.

doi: 10.3390/foods13223647

Figure Lengend Snippet: Figure 5. Mechanism analyses for prostate hyperplasia. Testosterone levels (A), 5α-reductase levels (B), DHT levels (C), AR levels (D), and PSA levels (E) are all derived from the ELISA kit. Values are mean ± SD from five independent tests in triplicates compared to control values (0% line). * p < 0.05 vs. control; ** p < 0.05 vs. single agents; # p < 0.05 vs. DHT.

Article Snippet: According to the manufacturer, a Human Dihydrotestosterone ELISA Kit (Cusabio, Houston, TX, USA) was used to measure DHT in co-culture prostatic supernatants [43].

Techniques: Derivative Assay, Enzyme-linked Immunosorbent Assay, Control

Figure 6. Serotonin and proliferation studies. The following results are derived from an ELISA kit: (A) 5-Htr1a levels, (B) serotonin production, (C) Ki67 expression, and (D) proliferation rate. The mean ± SD of five separate, duplicate tests is presented, along with * p < 0.05 vs. control, ** p < 0.05 vs. single drugs, and # p < 0.05 vs. DHT, in comparison to control values (0% line).

Journal: Foods (Basel, Switzerland)

Article Title: Analysis of the Beneficial Effects of Probiotics on the Gut-Prostate Axis Using Prostatic Co-Culture Model.

doi: 10.3390/foods13223647

Figure Lengend Snippet: Figure 6. Serotonin and proliferation studies. The following results are derived from an ELISA kit: (A) 5-Htr1a levels, (B) serotonin production, (C) Ki67 expression, and (D) proliferation rate. The mean ± SD of five separate, duplicate tests is presented, along with * p < 0.05 vs. control, ** p < 0.05 vs. single drugs, and # p < 0.05 vs. DHT, in comparison to control values (0% line).

Article Snippet: According to the manufacturer, a Human Dihydrotestosterone ELISA Kit (Cusabio, Houston, TX, USA) was used to measure DHT in co-culture prostatic supernatants [43].

Techniques: Derivative Assay, Enzyme-linked Immunosorbent Assay, Expressing, Control, Comparison