2016
DOI: 10.1111/and.12533
|View full text |Cite
|
Sign up to set email alerts
|

Biphasic effect ofSyzygium aromaticumflower bud on reproductive physiology of male mice

Abstract: The flower buds of Syzygium aromaticum (clove) have been used for the treatment of male sexual disorders in indigenous medicines of Indian subcontinent. Therefore to evaluate the efficacy of Syzygium aromaticum on the male reproductive health, chronic oral exposure of aqueous extract of flower buds of Syzygium in three doses (15 mg, 30 mg and 60 mg kg BW) were studied for a single spermatogenic cycle (35 days) in Parkes (P) strain mice. Lower dose (15 mg) of Syzygium aromaticum flower buds increased serum test… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
13
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 15 publications
(13 citation statements)
references
References 27 publications
0
13
0
Order By: Relevance
“…Further, the present study indicates that Shilajit may stimulate testosterone biosynthesis by increasing the activity of testicular hydroxysteroid dehydrogenases. Pituitary gonadotropins are prime regulators of testicular androgenic enzymes activities; therefore, the increase in the activities of testicular Δ 5 3β‐HSD and 17β‐HSD may be due to the effect of Shilajit on pituitary gonadotropins secretion (Mishra & Singh, ; Verma & Singh, ). It is, therefore, reasonable to assume that Shilajit improves the functional status of male reproductive organs and the related endocrine pathways through pituitary–testicular axis, presumably by acting as an antioxidant; however, this needs further investigations.…”
Section: Discussionmentioning
confidence: 99%
See 2 more Smart Citations
“…Further, the present study indicates that Shilajit may stimulate testosterone biosynthesis by increasing the activity of testicular hydroxysteroid dehydrogenases. Pituitary gonadotropins are prime regulators of testicular androgenic enzymes activities; therefore, the increase in the activities of testicular Δ 5 3β‐HSD and 17β‐HSD may be due to the effect of Shilajit on pituitary gonadotropins secretion (Mishra & Singh, ; Verma & Singh, ). It is, therefore, reasonable to assume that Shilajit improves the functional status of male reproductive organs and the related endocrine pathways through pituitary–testicular axis, presumably by acting as an antioxidant; however, this needs further investigations.…”
Section: Discussionmentioning
confidence: 99%
“…In mice spermatogenesis, developing spermatids spend 4.84 days in step 14–16. Therefore, to calculate daily sperm production, the number of steps 14–16 spermatids was divided by 4.84 (Mishra & Singh, ).…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Testicular cholesterol concentration was determined by the enzymatic end‐point method using commercially available kits (BioAssay Systems) according to the protocol of the manufacturer. As used by Mishra and Singh (2016), the method of Talalay (1962) was used to measure the activity of 3β‐HSD, while the method of Jarabak, Adams, Williams‐Ashman, and Talalay (1962) was used to measure 17β‐HSD activity in the testis. In a total volume of 2 ml, the reaction mixture contained 100 μmol sodium pyrophosphate buffer (pH 8.9), 0.5 μmol NAD + for 3β‐HSD and NADP + for 17β‐HSD, 0.14 μmol dehydroepiandrosterone for 3β‐HSD and 0.5 μmol testosterone for 17β‐HSD, and 20 mg equivalent of microsomal protein as enzyme source.…”
Section: Methodsmentioning
confidence: 99%
“…Cholesterol was assayed in the sample by the enzymatic end‐point method using a commercially available kit (Randox, UK) following the manufacturer's protocol. Testicular 3β‐HSD and 17β‐HSD activities were measured according to the methods of Talalay () and Jarabak, Adams, Williams‐Ashman, and Talalay (), respectively, as used by Mishra and Singh (). The reaction mixture in a total volume of 2 ml contained 100 μmol sodium pyrophosphate buffer (pH 8.9), 0.5 μmol NAD+ for 3β‐HSD and NADP+ for 17β‐HSD, 0.14 μmol dehydroepiandrosterone for 3β‐HSD and 0.5 μmol testosterone for 17β‐HSD, and 20 mg equivalent of microsomal protein as enzyme source.…”
Section: Methodsmentioning
confidence: 99%