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Thermo Fisher gene exp bmp4 rn00432087 m1
<t>Bmp4</t> , Bmp5 , and Inhba expression in the ovaries. (A–C) Relative mRNA expression quantified by real-time PCR. Expression levels are relative to 18S ribosomal RNA. Data are shown as mean ± standard deviation with individual data points. P -values were obtained by one-way analysis of variance (ANOVA) with Tukey’s post hoc test (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). (D–G) Correlation analysis between gene expression and ovarian follicle counts in the DHT and DHT+TSS groups ( n = 6 per group). The correlation coefficient ( r 2 ) and P -value were calculated. DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; PCR, polymerase chain reaction.
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<t>Bmp4</t> , Bmp5 , and Inhba expression in the ovaries. (A–C) Relative mRNA expression quantified by real-time PCR. Expression levels are relative to 18S ribosomal RNA. Data are shown as mean ± standard deviation with individual data points. P -values were obtained by one-way analysis of variance (ANOVA) with Tukey’s post hoc test (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). (D–G) Correlation analysis between gene expression and ovarian follicle counts in the DHT and DHT+TSS groups ( n = 6 per group). The correlation coefficient ( r 2 ) and P -value were calculated. DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; PCR, polymerase chain reaction.
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<t>Bmp4</t> , Bmp5 , and Inhba expression in the ovaries. (A–C) Relative mRNA expression quantified by real-time PCR. Expression levels are relative to 18S ribosomal RNA. Data are shown as mean ± standard deviation with individual data points. P -values were obtained by one-way analysis of variance (ANOVA) with Tukey’s post hoc test (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). (D–G) Correlation analysis between gene expression and ovarian follicle counts in the DHT and DHT+TSS groups ( n = 6 per group). The correlation coefficient ( r 2 ) and P -value were calculated. DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; PCR, polymerase chain reaction.
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Bmp4 , Bmp5 , and Inhba expression in the ovaries. (A–C) Relative mRNA expression quantified by real-time PCR. Expression levels are relative to 18S ribosomal RNA. Data are shown as mean ± standard deviation with individual data points. P -values were obtained by one-way analysis of variance (ANOVA) with Tukey’s post hoc test (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). (D–G) Correlation analysis between gene expression and ovarian follicle counts in the DHT and DHT+TSS groups ( n = 6 per group). The correlation coefficient ( r 2 ) and P -value were calculated. DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; PCR, polymerase chain reaction.

Journal: Frontiers in Endocrinology

Article Title: Amelioration of polycystic ovarian morphology by Tokishakuyakusan in a PCOS rat model: association with bone morphogenetic protein 4

doi: 10.3389/fendo.2025.1649124

Figure Lengend Snippet: Bmp4 , Bmp5 , and Inhba expression in the ovaries. (A–C) Relative mRNA expression quantified by real-time PCR. Expression levels are relative to 18S ribosomal RNA. Data are shown as mean ± standard deviation with individual data points. P -values were obtained by one-way analysis of variance (ANOVA) with Tukey’s post hoc test (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). (D–G) Correlation analysis between gene expression and ovarian follicle counts in the DHT and DHT+TSS groups ( n = 6 per group). The correlation coefficient ( r 2 ) and P -value were calculated. DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; PCR, polymerase chain reaction.

Article Snippet: The following TaqMan primer–probe sets (Thermo Fisher Scientific) were used: Bmp4 , Rn00432087_m1; Bmp5 , Rn01447676_m1; inhibin-βa ( Inhba ), Rn01538592_m1; steroidogenic acute regulatory protein ( Star ), Rn00580695_m1; cytochrome P450 11A1 ( Cyp11a1 ), Rn00568733_m1; 3β hydroxysteroid dehydrogenase ( Hsd3b ), Rn01789220_m1; 18s , Hs99999901_s1; and Gapdh , Rn01775763_g1.

Techniques: Expressing, Real-time Polymerase Chain Reaction, Standard Deviation, Gene Expression, Polymerase Chain Reaction

BMP4 and inhibin βA protein expression in the ovaries. (A) Representative Western blot images. (B, C) Quantification of BMP4 and inhibin βA protein levels relative to β-actin. Data are shown as mean ± standard deviation with individual data points (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). * P < 0.05, ** P < 0.01, one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test; P < 0.0167 by Bonferroni correction. BMP, bone morphogenetic protein; DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan.

Journal: Frontiers in Endocrinology

Article Title: Amelioration of polycystic ovarian morphology by Tokishakuyakusan in a PCOS rat model: association with bone morphogenetic protein 4

doi: 10.3389/fendo.2025.1649124

Figure Lengend Snippet: BMP4 and inhibin βA protein expression in the ovaries. (A) Representative Western blot images. (B, C) Quantification of BMP4 and inhibin βA protein levels relative to β-actin. Data are shown as mean ± standard deviation with individual data points (vehicle: n = 6; DHT: n = 9; DHT+TSS: n = 10). * P < 0.05, ** P < 0.01, one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test; P < 0.0167 by Bonferroni correction. BMP, bone morphogenetic protein; DHT, 5α-dihydrotestosterone; TSS, Tokishakuyakusan.

Article Snippet: The following TaqMan primer–probe sets (Thermo Fisher Scientific) were used: Bmp4 , Rn00432087_m1; Bmp5 , Rn01447676_m1; inhibin-βa ( Inhba ), Rn01538592_m1; steroidogenic acute regulatory protein ( Star ), Rn00580695_m1; cytochrome P450 11A1 ( Cyp11a1 ), Rn00568733_m1; 3β hydroxysteroid dehydrogenase ( Hsd3b ), Rn01789220_m1; 18s , Hs99999901_s1; and Gapdh , Rn01775763_g1.

Techniques: Expressing, Western Blot, Standard Deviation

Effect of Tokishakuyakusan (TSS) on target gene expressions in granulosa cells (GCs) derived from prenatally 5α-dihydrotestosterone (DHT)-treated rats. (A) Timeline of ovarian GC collection. (B, C) Relative mRNA expression of Bmp4 and Inhba in primary cultured GCs after 24 h of TSS treatment (125–500 μg/mL). Expression levels are relative to Gapdh . Data are shown as mean ± standard deviation with individual data points ( n = 3 per group). ** P < 0.01, P -values for the untreated control were obtained using one-way analysis of variance (ANOVA) followed by Dunnett’s post hoc test. PMSG, pregnant mare serum gonadotropin; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; Gapdh, glyceraldehyde-3-phosphate dehydrogenase.

Journal: Frontiers in Endocrinology

Article Title: Amelioration of polycystic ovarian morphology by Tokishakuyakusan in a PCOS rat model: association with bone morphogenetic protein 4

doi: 10.3389/fendo.2025.1649124

Figure Lengend Snippet: Effect of Tokishakuyakusan (TSS) on target gene expressions in granulosa cells (GCs) derived from prenatally 5α-dihydrotestosterone (DHT)-treated rats. (A) Timeline of ovarian GC collection. (B, C) Relative mRNA expression of Bmp4 and Inhba in primary cultured GCs after 24 h of TSS treatment (125–500 μg/mL). Expression levels are relative to Gapdh . Data are shown as mean ± standard deviation with individual data points ( n = 3 per group). ** P < 0.01, P -values for the untreated control were obtained using one-way analysis of variance (ANOVA) followed by Dunnett’s post hoc test. PMSG, pregnant mare serum gonadotropin; Bmp, bone morphogenetic protein; Inhba, inhibin-βa; Gapdh, glyceraldehyde-3-phosphate dehydrogenase.

Article Snippet: The following TaqMan primer–probe sets (Thermo Fisher Scientific) were used: Bmp4 , Rn00432087_m1; Bmp5 , Rn01447676_m1; inhibin-βa ( Inhba ), Rn01538592_m1; steroidogenic acute regulatory protein ( Star ), Rn00580695_m1; cytochrome P450 11A1 ( Cyp11a1 ), Rn00568733_m1; 3β hydroxysteroid dehydrogenase ( Hsd3b ), Rn01789220_m1; 18s , Hs99999901_s1; and Gapdh , Rn01775763_g1.

Techniques: Derivative Assay, Expressing, Cell Culture, Standard Deviation, Control

Effect of Tokishakuyakusan (TSS) on progesterone synthesis in granulosa cells (GCs) derived from prenatally 5α-dihydrotestosterone (DHT)-treated rats. (A–D) Relative mRNA expression of Bmp4 (A) , Star (B) , Cyp11a1 (C) , and Hsd3b (D) in primary cultured GCs after 24 h of TSS (500 μg/mL) treatment with or without FSH (3 ng/mL). Expression levels are relative to Gapdh. (E) Progesterone concentration in GC culture medium after 24 h of treatment. Data are shown as mean ± standard deviation with individual data points ( n = 3 per group). * P < 0.05, ** P < 0.01, two-way analysis of variance (ANOVA) followed by Tukey’s post hoc test. FSH, follicle-stimulating hormone; Star, steroidogenic acute regulatory protein; Cyp11a1, cytochrome P450 11A1; Hsd3b, 3β hydroxysteroid dehydrogenase; Gapdh, glyceraldehyde-3-phosphate dehydrogenase.

Journal: Frontiers in Endocrinology

Article Title: Amelioration of polycystic ovarian morphology by Tokishakuyakusan in a PCOS rat model: association with bone morphogenetic protein 4

doi: 10.3389/fendo.2025.1649124

Figure Lengend Snippet: Effect of Tokishakuyakusan (TSS) on progesterone synthesis in granulosa cells (GCs) derived from prenatally 5α-dihydrotestosterone (DHT)-treated rats. (A–D) Relative mRNA expression of Bmp4 (A) , Star (B) , Cyp11a1 (C) , and Hsd3b (D) in primary cultured GCs after 24 h of TSS (500 μg/mL) treatment with or without FSH (3 ng/mL). Expression levels are relative to Gapdh. (E) Progesterone concentration in GC culture medium after 24 h of treatment. Data are shown as mean ± standard deviation with individual data points ( n = 3 per group). * P < 0.05, ** P < 0.01, two-way analysis of variance (ANOVA) followed by Tukey’s post hoc test. FSH, follicle-stimulating hormone; Star, steroidogenic acute regulatory protein; Cyp11a1, cytochrome P450 11A1; Hsd3b, 3β hydroxysteroid dehydrogenase; Gapdh, glyceraldehyde-3-phosphate dehydrogenase.

Article Snippet: The following TaqMan primer–probe sets (Thermo Fisher Scientific) were used: Bmp4 , Rn00432087_m1; Bmp5 , Rn01447676_m1; inhibin-βa ( Inhba ), Rn01538592_m1; steroidogenic acute regulatory protein ( Star ), Rn00580695_m1; cytochrome P450 11A1 ( Cyp11a1 ), Rn00568733_m1; 3β hydroxysteroid dehydrogenase ( Hsd3b ), Rn01789220_m1; 18s , Hs99999901_s1; and Gapdh , Rn01775763_g1.

Techniques: Derivative Assay, Expressing, Cell Culture, Concentration Assay, Standard Deviation