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1.
Transgenic Res ; 26(4): 567-575, 2017 08.
Article in English | MEDLINE | ID: mdl-28534229

ABSTRACT

Swine are the only livestock species that produce both the second mammalian isoform of gonadotropin-releasing hormone (GNRH2) and its receptor (GNRHR2). Previously, we reported that GNRH2 and GNRHR2 mediate LH-independent testosterone secretion from porcine testes. To further explore this ligand-receptor complex, a pig model with reduced GNRHR2 expression was developed. Small hairpin RNA sequences targeting porcine GNRHR2 were subcloned into a lentiviral-based vector, lentiviral particles were generated and microinjected into the perivitelline space of zygotes, and embryos were transferred into a recipient. One GNRHR2 knockdown (KD) female was born that subsequently produced 80 piglets from 6 litters with 46 hemizygous progeny (57% transgenic). Hemizygous GNRHR2 KD (n = 10) and littermate control (n = 7) males were monitored at 40, 100, 150, 190, 225 and 300 days of age; body weight and testis size were measured and serum was isolated and assayed for testosterone and luteinizing hormone (LH) concentrations. Body weight of GNRHR2 KD boars was not different from littermate controls (P = 0.14), but testes were smaller (P < 0.05; 331.8 vs. 374.8 cm3, respectively). Testosterone concentrations tended (P = 0.06) to be reduced in GNRHR2 KD (1.6 ng/ml) compared to littermate control (4.2 ng/ml) males, but LH levels were similar (P = 0.47). The abundance of GNRHR2 mRNA was reduced (P < 0.001) by 69% in testicular tissue from mature GNRHR2 KD (n = 5) versus littermate control (n = 4) animals. These swine represent the first genetically-engineered model to elucidate the function of GNRH2 and its receptor in mammals.


Subject(s)
Animals, Genetically Modified/genetics , Gonadotropin-Releasing Hormone/genetics , Receptors, LHRH/genetics , Animals , Animals, Genetically Modified/growth & development , Female , Gene Expression Regulation , Gene Knockdown Techniques , Gonadotropin-Releasing Hormone/biosynthesis , Hemizygote , Luteinizing Hormone/blood , Male , RNA, Small Interfering/genetics , Receptors, LHRH/biosynthesis , Swine/genetics , Swine/growth & development , Testis/growth & development , Testis/metabolism , Testosterone/blood
2.
J Therm Biol ; 57: 84-91, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27033043

ABSTRACT

Boars from sows with elevated plasma cortisol during pregnancy have shorter anogenital distance (AGD), a trait associated with subfertility. Since gestating sows often experience summer heat stress (HS), a mouse model was used to evaluate the effect of prenatal HS on AGD and fertility; efficacy of the heat stress-mitigating supplement Artemisia absinthium (AB) was also evaluated. Dams were treated from d 8-18 of gestation, residing in ambient temperatures from 0700 to 1900h. From 1900 to 0700h females were exposed to 34.13±0.27°C (HS) with access to water (HSW; n=9), HS with access to a 1% w/v decoction of AB (HSA; n=9), 20.81±0.20°C (thermal neutral; TN) with water (TNW; n=10) or TN with AB (TNA; n=10). Daily liquid consumption was measured from d 6-18, and tail temperature was recorded at 0700 and 1900h from d 8-18. Progeny weight and AGD were recorded at birth and weaning. At maturity, males were mated to non-littermate females from each treatment; these females were euthanized after 16 d of TN gestation. Reproductive traits were compared among all male/female treatment combinations; testes were weighed. Average liquid intake differed among treatments with HS and AB animals drinking more (P<0.0004). A treatment by time interaction for tail temperature (P<0.001) was observed; HS increased tail temperature of HSA and HSW animals similarly compared to TNA and TNW. Treatment affected (P<0.01) male birth AGD (HSW shortest; P<0.07). At maturity, HSW males also had the smallest testes (P<0.02). However, we observed no differences in fertility (P>0.10). These data indicate that in utero HS decreases both male birth AGD and adult testis size, effects which maternal AB consumption mitigates.


Subject(s)
Artemisia absinthium/chemistry , Heat-Shock Response , Plant Extracts/pharmacology , Prenatal Exposure Delayed Effects/drug therapy , Testis/embryology , Animals , Female , Male , Mice , Plant Extracts/therapeutic use , Pregnancy , Prenatal Exposure Delayed Effects/etiology , Testis/abnormalities , Testis/drug effects
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