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The animal model deals with the species other than the human, as it can imitate the disease progression, its’ diagnosis as well as a treatment similar to human. Discovery of a drug and/or component, equipment, their toxicological studies, dose, side effects are in vivo studied for future use in humans considering its’ ethical issues. Here lies the importance of the animal model for its enormous use in biomedical research. Animal models have many facets that mimic various disease conditions in humans like systemic autoimmune diseases, rheumatoid arthritis, epilepsy, Alzheimer’s disease, cardiovascular diseases, Atherosclerosis, diabetes, etc., and many more. Besides, the model has tremendous importance in drug development, development of medical devices, tissue engineering, wound healing, and bone and cartilage regeneration studies, as a model in vascular surgeries as well as the model for vertebral disc regeneration surgery. Though, all the models have some advantages as well as challenges, but, present review has emphasized the importance of various small and large animal models in pharmaceutical drug development, transgenic animal models, models for medical device developments, studies for various human diseases, bone and cartilage regeneration model, diabetic and burn wound model as well as surgical models like vascular surgeries and surgeries for intervertebral disc degeneration considering all the ethical issues of that specific animal model. Despite, the process of using the animal model has facilitated researchers to carry out the researches that would have been impossible to accomplish in human considering the ethical prohibitions.

Ultrafast processes in matter, such as the electron emission after light absorption, can now be studied using ultrashort light pulses of attosecond duration (10−18 seconds) in the extreme ultraviolet spectral range. The lack of spectral resolution due to the use of short light pulses has raised issues in the interpretation of the experimental results and the comparison with theoretical calculations. We determine photoionization time delays in neon atoms over a 40–electron volt energy range with an interferometric technique combining high temporal and spectral resolution. We spectrally disentangle direct ionization from ionization with shake-up, in which a second electron is left in an excited state, and obtain excellent agreement with theoretical calculations, thereby solving a puzzle raised by 7-year-old measurements.

The discovery of a significantly large anomalous Hall effect in the chiral antiferromagnetic system—Mn3Ge—indicates that the Weyl points are widely separated in phase space and positioned near the Fermi surface. In order to examine the effects of Fe substitution in Mn3Ge on the presence and location of the Weyl points, we synthesized (Mn1−αFeα)3Ge (α=0−0.30) compounds. The AHE was observed in compounds up to α = 0.22, but only within the temperature range where the magnetic structure remains the same as the Mn3Ge. Additionally, positive longitudinal magnetoconductance and planar Hall effect (PHE) were detected within the same temperature and doping range. These findings strongly suggest the existence of Weyl points in (Mn1−αFeα)3Ge (α=0−0.22) compounds. Further, we observed that with an increase in Fe doping fraction, there is a significant reduction in the magnitude of anomalous Hall conductivity, PHE, and positive longitudinal magnetoconductance, indicating that the Weyl points move further away from the Fermi surface. Consequently, it can be concluded that suitable dopants in the parent Weyl semimetals have the potential to tune the properties of Weyl points and the resulting anomalous electrical transport effects.

A bstract We consider the collider phenomenology of a simple extension of the Standard Model (SM), which consists of an EW isospin 3/2 scalar, Δ and a pair of EW isospin 1 vector like fermions, Σ and Σ ¯ , responsible for generating tiny neutrino mass via the effective dimension seven operator. This scalar quadruplet with hypercharge Y = 3 has a plethora of implications at the collider experiments. Its signatures at TeV scale colliders are expected to be seen, if the quadruplet masses are not too far above the electroweak symmetry breaking scale. In this article, we study the phenomenology of multi-charged quadruplet scalars. In particular, we study the multi-lepton signatures at the Large Hadron Collider (LHC) experiment, arising from the production and decays of triply and doubly charged scalars. We studied Drell-Yan (DY) pair production as well as pair production of the charged scalars via photon-photon fusion. For doubly and triply charged scalars, photon fusion contributes significantly for large scalar masses. We also studied LHC constraints on the masses of doubly charged scalars in this model. We derive a lower mass limit of 725 GeV on doubly charged quadruplet scalar.

Photoionization as a half-scattering process is not instantaneous. Usually, time delays in photoionization are on the order of tens of attoseconds. In going from a single atom to a nano-object, one can expect the delay to increase, since the photoelectron scatters over a larger distance. Here we show that this intuition is not correct when comparing three-dimensional and planar molecules. Using attosecond interferometry, we find that the time delays in two-dimensional (2D) carbon-based molecules can be significantly shorter than those of three-dimensional counterparts. The measured time delay carries the signature of the spatial distribution of the 2D hole created in the residual molecular cation, allowing us to obtain its dimensions with angstrom accuracy. Our results demonstrate that the photoionization delay depends on the symmetry and shape of the created hole, as we show by identifying a quadrupole contribution in the measured delay of 2D molecules. Attosecond interferometry measurements of photoionization delays in planar carbon-based molecules can provide information on the dimension and shape of the two-dimensional hole generated in the process.

Canine parvovirus 2 (CPV-2) has been considered to be an important pathogen of domestic and wild canids and has spread worldwide since its emergence in 1978. It has been reported from Asia, Australia, New Zealand, the Americas and Europe. Two distinct parvoviruses are now known to infect dogs—the pathogenic CPV-2 and CPV-1 or the minute virus of canine (MVC). CPV-2, the causative agent of acute hemorrhagic enteritis and myocarditis in dogs, is one of the most important pathogenic viruses with high morbidity (100%) and frequent mortality up to 10% in adult dogs and 91% in pups. The disease condition has been complicated further due to emergence of a number of variants namely CPV-2a, CPV-2b and CPV-2c over the years and involvement of domestic and wild canines. There are a number of different serological and molecular tests available for prompt, specific and accurate diagnosis of the disease. Further, both live attenuated and inactivated vaccines are available to control the disease in animals. Besides, new generation vaccines namely recombinant vaccine, peptide vaccine and DNA vaccine are in different stages of development and offer hope for better management of the disease in canines. However, new generation vaccines have not been issued license to be used in the field condition. Again, the presence of maternal antibodies often interferes with the active immunization with live attenuated vaccine and there always exists a window of susceptibility in spite of following proper immunization regimen. Lastly, judicious use of the vaccines in pet dogs, stray dogs and wild canids keeping in mind the new variants of the CPV-2 along with the proper sanitation and disinfection practices must be implemented for the successful control the disease.

Glucagon-like peptide-1 receptor (GLP-1R) agonists, widely used to treat type 2 diabetes, reduce blood pressure (BP) in hypertensive patients. Whether this action involves central mechanisms is unknown. We here report that repeated lateral ventricular (LV) injection of GLP-1R agonist, liraglutide, once daily for 15 days counteracted the development of hypertension in spontaneously hypertensive rats (SHR). In parallel, it suppressed urinary norepinephrine excretion, and induced c-Fos expressions in the area postrema (AP) and nucleus tractus solitarius (NTS) of brainstem including the NTS neurons immunoreactive to dopamine beta-hydroxylase (DBH). Acute administration of liraglutide into fourth ventricle, the area with easy access to the AP and NTS, transiently decreased BP in SHR and this effect was attenuated after lesion of NTS DBH neurons with anti-DBH conjugated to saporin (anti-DBH-SAP). In anti-DBH-SAP injected SHR, the antihypertensive effect of repeated LV injection of liraglutide for 14 days was also attenuated. These findings demonstrate that the central GLP-1R signaling via NTS DBH neurons counteracts the development of hypertension in SHR, accompanied by attenuated sympathetic nerve activity.

In the mammalian model of sex determination, embryos are considered to be sexually indifferent until the transient action of a sex-determining gene initiates gonadal differentiation. Although this model is thought to apply to all vertebrates, this has yet to be established. Here we have examined three lateral gynandromorph chickens (a rare, naturally occurring phenomenon in which one side of the animal appears male and the other female) to investigate the sex-determining mechanism in birds. These studies demonstrated that gynandromorph birds are genuine male:female chimaeras, and indicated that male and female avian somatic cells may have an inherent sex identity. To test this hypothesis, we transplanted presumptive mesoderm between embryos of reciprocal sexes to generate embryos containing male:female chimaeric gonads. In contrast to the outcome for mammalian mixed-sex chimaeras, in chicken mixed-sex chimaeras the donor cells were excluded from the functional structures of the host gonad. In an example where female tissue was transplanted into a male host, donor cells contributing to the developing testis retained a female identity and expressed a marker of female function. Our study demonstrates that avian somatic cells possess an inherent sex identity and that, in birds, sexual differentiation is substantively cell autonomous.

We present results of a comprehensive investigation of two phenomena arising in superconductor(S)/ferromagnet(F) heterostructures of Nb on FePd with a lateral magnetic domain pattern: domain-superconductivity and spin-triplet Cooper pair generation. Resistivity measurements in a magnetic field applied out-of-plane to a Nb/FePd (S/F) sample with high magnetocrystalline anisotropy give evidence of stray field generated domain-wall- and reverse-domain-superconductivity. A corresponding bilayer comprising low magnetocrystalline anisotropy exhibits spin-triplet Cooper pair generation and a notable high variation of the S critical temperature due to spin-triplet generation (ΔTc) of 100 mK in an in-plane applied field. Using reference samples we can clearly distinguish stray field from proximity effects. The relevance of the characteristic S and F length scales related to the observed proximity effects is discussed.

Background Glucagon-like peptide-1 (GLP-1) induces diuresis and natriuresis. Previously we have shown that GLP-1 activates afferent renal nerve to increase efferent renal sympathetic nerve activity that negates the diuresis and natriuresis as a negative feedback mechanism in normal rats. However, renal effects of GLP-1 in heart failure (HF) has not been elucidated. The present study was designed to assess GLP-1-induced diuresis and natriuresis in rats with HF and its interactions with renal nerve activity. Methods HF was induced in rats by coronary artery ligation. The direct recording of afferent renal nerve activity (ARNA) with intrapelvic injection of GLP-1 and total renal sympathetic nerve activity (RSNA) with intravenous infusion of GLP-1 were performed. GLP-1 receptor expression in renal pelvis, densely innervated by afferent renal nerve, was assessed by real-time PCR and western blot analysis. In separate group of rats after coronary artery ligation selective afferent renal denervation (A-RDN) was performed by periaxonal application of capsaicin, then intravenous infusion of GLP-1-induced diuresis and natriuresis were evaluated. Results In HF, compared to sham-operated control; (1) response of increase in ARNA to intrapelvic injection of GLP-1 was enhanced (3.7 ± 0.4 vs. 2.0 ± 0.4 µV s), (2) GLP-1 receptor expression was increased in renal pelvis, (3) response of increase in RSNA to intravenous infusion of GLP-1 was enhanced (132 ± 30% vs. 70 ± 16% of the baseline level), and (4) diuretic and natriuretic responses to intravenous infusion of GLP-1 were blunted (urine flow 53.4 ± 4.3 vs. 78.6 ± 4.4 µl/min/gkw, sodium excretion 7.4 ± 0.8 vs. 10.9 ± 1.0 µEq/min/gkw). A-RDN induced significant increases in diuretic and natriuretic responses to GLP-1 in HF (urine flow 96.0 ± 1.9 vs. 53.4 ± 4.3 µl/min/gkw, sodium excretion 13.6 ± 1.4 vs. 7.4 ± 0.8 µEq/min/gkw). Conclusions The excessive activation of neural circuitry involving afferent and efferent renal nerves suppresses diuretic and natriuretic responses to GLP-1 in HF. These pathophysiological responses to GLP-1 might be involved in the interaction between incretin-based medicines and established HF condition. RDN restores diuretic and natriuretic effects of GLP-1 and thus has potential beneficial therapeutic implication for diabetic HF patients.