Ram Pratap Singh

Dr. Ram Pratap Singh


Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 October 2013 in Food Control
Verified
Journal Article
Closed access
RSRenu Singh
Renu Singh
AYA.S. Yadav
A.S. Yadav
VTV. Tripathi
V. Tripathi
RSRam Pratap Singh
Ram Pratap Singh

27 February 2015 in Environmental Toxicology and Chemistry
Verified
Journal Article
Closed access
PDF file
RSRam Pratap Singh
Ram Pratap Singh
CSChathathayil Mohammedali Shafeeque
Chathathayil Mohammedali Shafeeque
SSSanjeev K. Sharma
Sanjeev K. Sharma
NPNitin K. Pandey
Nitin K. Pandey
RSRenu Singh
Renu Singh
PAParappurath A. Azeez
Parappurath A. Azeez

1 October 2014 in Animal Reproduction Science
Verified
Journal Article
Closed access
CSChathathayil Mohammedali Shafeeque
Chathathayil Mohammedali Shafeeque
RSRam Pratap Singh
Ram Pratap Singh
SSS.K. Sharma
S.K. Sharma
JMJ. Mohan
J. Mohan
KSK.V.H. Sastry
K.V.H. Sastry
PAP.A. Azeez
P.A. Azeez

3 May 2018 in Reproduction, Fertility and Development
Verified
Journal Article
Closed access
PDF file
CTChommanart Thongkittidilok
Chommanart Thongkittidilok
RSRam Pratap Singh
Ram Pratap Singh
PCPierre Comizzoli
Pierre Comizzoli
DWDavid Wildt
David Wildt
NSNucharin Songsasen
Nucharin Songsasen
The aims of the present study were to determine the effects of insulin, in vitro, on: (1) the viability and growth of domestic cat ovarian follicles; (2) mRNA expression of genes regulating steroidogenesis (cytochrome P450 family 17 subfamily, A polypeptide 1 (Cyp17a1), cytochrome P450 family 19 subfamily, A polypeptide 1 (Cyp19a1) and steroidogenic acute regulatory protein (Star)) and water transport (aquaporins (AQPs) Aqp1, Aqp3, Aqp7, Aqp9); and (3) steroid production (17ß-oestradiol (E2), progesterone (P4), androstenedione (A4)). Cat secondary follicles were isolated from ovarian cortices and cultured in 0 (Control), 1 or 10 µg mL-1 insulin for 14 days (Day 0 = culture onset). Follicle and oocyte viability (based on neutral red staining), diameter and antrum formation were assessed every 72 h and at the end of incubation (Day 14). Expression of steroidogenic and water transport genes was evaluated on Days 0, 6 and 12, and E2, P4 and A4 concentrations in the culture medium were determined on Day 12. By Day 14, 1 and 10 µg mL-1 insulin had significantly promoted (P < 0.05) both antrum formation in a mean (± s.e.m.) 26.9 ± 9.0% and 78.0 ± 10.0% of follicles respectively, and follicle growth (diameter 151.4 ± 4.5 and 169.9 ± 10.5 µm respectively) compared with Control (antrum formation in 3.3 ± 3.3% of follicles and follicle diameter 129.1 ± 6.6 µm). High insulin (10 µg mL-1) treatment increased follicle viability compared with Control (86.0 ± 9.8% vs 38.1 ± 10.9% respectively; P < 0.05). However, insulin had no beneficial effect (P > 0.05) on oocyte diameter. Cyp17a1 expression on Days 6 and 12 was higher (P < 0.05) in follicles cultured in the low (1 µg mL-1) compared with high (10 µg mL-1) insulin treatment, with no significant difference between low or high insulin vs Control groups. Star expression was higher (P < 0.01) in the low insulin compared with Control group on Day 6, but Star was undetectable in the high insulin group by Day 12. Compared with high insulin, low insulin increased (P < 0.05) Aqp1 expression on Day 6, but there were no significant differences between these two groups on Day 12. In contrast, high insulin decreased (P < 0.05) Aqp9 transcript levels compared with Control. Only P4 production was affected by insulin, with P4 concentrations in the medium being higher (P < 0.05) in the low compared with high insulin and Control groups. In summary, the findings indicate that insulin promotes cat ovarian follicle growth and survival in vitro, including enhanced antrum formation, with the likely mechanism involving temporal expression of Cyp17a1, Star and Aqp9 genes.

15 March 2014 in Asian Journal of Animal and Veterinary Advances
Verified
Journal Article
Closed access
Kuldeep DhamaKuldeep Dhama
Kuldeep Dhama
RSRam Pratap Singh
Ram Pratap Singh
KKK. Karthik
K. Karthik
SCS. Chakrabort
S. Chakrabort
RTR. Tiwari
R. Tiwari
JMJ. Mohan
J. Mohan
Artificial Insemination in Poultry and Possible Transmission of Infectious Pathogens: A Review

20 October 2011 in Reproduction, Fertility and Development
Verified
Journal Article
Closed access
PDF file
RSRam Pratap Singh
Ram Pratap Singh
KSK. V. H. Sastry
K. V. H. Sastry
NPN. K. Pandey
N. K. Pandey
KSK. B. Singh
K. B. Singh
IMI. A. Malecki
I. A. Malecki
RMR. P. Moudgal
R. P. Moudgal
The adult male Japanese quail has a well developed cloacal gland that produces meringue-like white foam. The physiological significance of the cloacal gland and its foam is still unclear. Therefore, we conducted two experiments to establish the functional role of the cloacal gland and its foam in natural mating and oviducal sperm transport. In the first experiment, artificial insemination of equal numbers of spermatozoa diluted in foam extract and normal saline once in a week were used to determine the role of foam in sperm transport in the female oviduct. After artificial insemination, eggs were collected to measure fertility, the duration of the fertile period, sperm holes and attached spermatozoa in the perivitelline membrane. Higher (P < 0.05) fertility and greater duration of the fertile period were observed when semen was inseminated along with foam extract compared with normal saline. Further, the sperm holes and trapped spermatozoa in the perivitelline membrane were also higher (P < 0.05) in the presence of foam extract. In the second experiment, two males with bigger and smaller cloacal gland areas were allowed to mate with a female. The mating attempts of males with larger cloacal gland were more successful (P < 0.05) than males with smaller cloacal glands. Our results indicated that cloacal foam improves sperm transport in the female oviduct and that males with larger cloacal gland areas are preferred during mating.