High-intensity interval resistance training (HIIRT) improves liver gluconeogenesis from lactate in Swiss mice

High-intensity physical exercise favors anaerobic glycolysis and increases lactatemia. Lactate is converted back to glucose in the liver, so that the lactate threshold, an indicator of physical performance, must be related to the gluconeogenic capacity of the liver. This research assessed the effect of a high-intensity interval resistance training (HIIRT) on liver gluconeogenesis from lactate. Swiss mice were trained (groups T) on vertical ladder with overload of 90% of their maximal load. Control animals remained untrained (groups C0 and C8). In situ liver perfusion with lactate and adrenaline was performed in rested mice after six hours of food deprivation. There were larger outputs of glucose (T6 71.90%, T8 54.53%) and pyruvate (T8 129.28%) (representative values for 4 mM lactate) in the groups trained for six or eight weeks (T6 and T8), and of glucose in the presence of adrenaline in group T8 (280%). The content of PEPCK, an important regulatory enzyme of the gluconeogenic pathway, was 69.13% higher in group T8 than in the age-matched untrained animals (C8). HIIRT augmented liver gluconeogenesis from lactate and this might improve the lactate threshold. Bullet points: The liver metabolizes lactate from muscle into glucose. Physical training may enhance the gluconeogenic capacity of the liver. As lactate clearance by the liver improves, lactate threshold is displaced to higher exercise intensities.

Spontaneous pre-axial polydactyly in Swiss mice

ABSTRACT: Spontaneous polydactyly has been described in several species, but only one report about it in Swiss mice. The aim of the current study was to report the spontaneous occurrence of pre-axial polydactyly in Swiss mice. Clinical examination showed one extra toe laterally to the first digit, in the plantar region, alopecia in the back, altered face growth anatomy and changed perineal region anatomy. Pre-axial polydactyly in the tibial side, fused metatarsals and Y-shaped free phalanges were evidenced in the radiographic images. Pre-axial polydactyly observed in the plantar region differed from that in reports on albino Swiss mice with post-axial polydactyly (Po/Po+) phenotype featured by one extra toe in the ulnar side of one, or both, front limbs, which is the dominant feature. The observed findings highlight the importance of both clinical examinations and close attention by professionals involved in rodents’ breeding on physical changes resulting from different causes, including the genetic ones, since they reveal mutations and, sometimes, new biomodels.

Histological and Weight Changes in the Testes of Plasmodium Berghei- Infected Swiss Mice Treated with Chloroquine

Chloroquine has gained great emphasis in the treatment of malaria. This study sought experimentally to determine the histomorphological and weight changes in the testes of male mice infected with Plasmodium berghei and treated with chloroquine. The study used 30 Swiss mice divided into five groups. Group 1 is Control that was not infected with Plasmodium berghei and not treated with chloroquine as control, Group 2 is Plasmodium (Plasmodiul berghei) Infected animals but not treated, Group 3 is Plasmodium Infected animals + Chloroquine (5mg/kg), Group 4 is Plasmodium Infected animals + Chloroquine (10mg/kg) and Group 5 is Plasmodium Infected animals + Chloroquine (15mg/kg). The mice were treated for 7 days after parasitaemia was confirmed and the Group 2-5 testes studied with reference to Group 1. The results showed that the Group 2 showed a little distortion, difference in spermatogenic activities and increased cellular activities; Group 3 showed large, convoluted tubules, moderate number of spermatids and large interstitial spaces, Group 4 showed Large seminiferous tubules, large spermatids, increased distortion and group 5 showed shrinking of seminiferous tubules, degeneration of interstitial cells of Leydig cells and Sertolic cells with spermatids. Groups 1-5 showed no significant effect in in body weights and testes weights of Swiss mice. Plasmodium berghei (malaria) and chloroquine have effects on histomorphological structures of Swiss mice testes but not on their teste’s weights. The testicular section from Swiss mice infected with malaria and treated at various doses when compared with the Control (Group 1) showed some moderate distortion in some structures like seminiferous tubules, connective tissues between the tubules, lumen and interstitial spaces. It can be deducted that Plasmodium berghei which caused parasitaemia in mice could cause a little tissue effect on mice if not treated.

The evaluation of acute and subchronic toxicities of An Phu Khang capsules in experimental animals

The purpose of this research was to evaluate the acute and subchronic toxicities of An Phu Khang capsules through oral administration in experimental animals. The acute toxicity was determined by the method of Litchfield Wilcoxon in Swiss mice. The subchronic toxicity was evaluated by the recommendation of WHO in Wistar rats at these doses of 0.54 g/kg b.w/day (equal to recommended human dose) and 1.62 g/kg b.w/day (3 times as high as recommended human dose) in 4 consecutive weeks. As a result, An Phu Khang capsules at the highest dose used for mice (36.29 g/kg b.w) did not show acute toxicity in mice. In terms of the subchronic toxicity test, after oral administration of An Phu Khang capsules, hematological parameters, hepato-renal functions, and microscopic images of liver and kidney at both doses were unchanged compared with the control group. In conclusion, An Phu Khang with both doses 0.54 g/kg b.w/day and 1.62 g/kg b.w/day did not produce acute and subchronic toxicities in Swiss mice and Wistar rats.

The study of acute and subchronic toxicities of Da Dai Trang HVD capsules in experimental animals

The purpose of this research is to evaluate the acute and subchronic toxicities of DA DAI TRANG HVD capsules through oral administration in experimental animals. The acute toxicity was determined by the method of Litchfield Wilcoxon in Swiss mice. The subchronic toxicity was evaluated by the recommendation of WHO and OECD in Wistar rats with oral doses of 1.44 g/kg/day (equal to recommended human dose) and 4.32 g/kg/day (3 times as high as recommended human dose) in 4 consecutive weeks. As a result, DA DAI TRANG HVD capsules at the highest dose used for mice (99.9 g materials/kg) did not express acute toxicity in mice. In term of the subchonic toxicity test, DA DAI TRANG HVD had no deleterious effect on hematological parameters, hepato-renal functions, macroscopic and microscopic images of livers and kidneys of rats. In conclusion, DA DAI TRANG HVD capsules did not produce the acute and subchronic toxicities in Swiss mice and Wistar rats.

Evaluation effects of “An Tri Khang” hard capsule on scopolamine-induced memory impairment in experimental animals

This study was performed to investigate the effects of An Tri Khang (ATK) hard capsule on scopolamine-induced memory impairment in experimental animals. The effects on memory of oral administration ATK were evaluated on scopolamine-induced memory impairment in experimental animals. The memory improvement effects were conducted on 2 experimental models: the Morris water maze (MWM) and the Multi-T maze (MTM). In the MWM model, ATK significantly reduced the time spent and pathlength to platform, increased the percentage of time swimming in platform’s quadrant. Swiss mice performed the MTM with shorter in both the time spent and the pathlength to the goal box (p < 0.01). Both doses of ATK attenuated scopolamine-mediated impairment of memory. ATK has potential effects on memory improvement. It is suggested that further clinical trials should be undertaken to have thorough assessment on human.

Effect of biotherapy T. cruzi 7x in several therapeutic schemes on experimental infection by Trypanosoma cruzi

Background: Biotherapy is used against infectious diseases treatment and prophylaxis and has been investigated by many researchers [1,2]. Aim: Assess the effect of biotherapy 7x T. cruzi on several treatment schemes, upon experimental infection by T. cruzi. Methodology: A blind, controlled and randomized by drawing experiment was performed. Male Swiss mice, four weeks old were utilized. Groups evaluated: IC – Infection Control (treated with water – 9 animals); TBBA7x3days – Treated with biotherapy 7x 3 days before and 3 days after infection (5 animals); TBB7x3days – Treated with 7x biotherapy 3 days before infection (5 animals); TBBAI7x3days – Treated with 7x biotherapy 3 days before infection and after infection indefinitely (6 animals). Animals were inoculated intraperitoneally with 1400 blood trypomastigotes Y strain. Biotherapy: prepared according to Farmacopéia Homeopática Brasileira [3]. Treatment plan: offered ad libitum, in the water (10µL/mL). Parasitological parameters: parasitemia was assessed according Brener’s technique. [4]. Clinical parameters: body hair aspect, edema, movement, diarrhea, body weight, temperature, food and water intake. Ethics: Registration 030/2008 UEM Ethics Committee for Experiments in Animals. Statistical analysis: was performed using the tests Kruskal Wallis and Mann-Whitney testes, significance 5%. Results: The best effect obtained was with the TBBA7x3days, both for clinical and parasitological parameters. It was expressed by lower parasitemia curve (p=0.04) and decrease of patent period tendency, of total parasitemia, of mortality and survival of the animals increase (Table 1). Evolution of parasitemia was distinct for the several treatment schemes. Survival of at least one mouse by treated groups is an extremely important data, since Y strain causes 100% mortality in Swiss mice. TBBAI7x3days group showed begger tendency in raising total parasitemia compared with IC. Although it might have occurred, this group presented 80% mortality rate compared with other groups. Animals from TBBA7x3days also showed better evolution of weight body, temperature, food (p=0.078-10%) and water intake, body hair aspect and edema development. Diarrhea and paralysis were only observed in IC group mice, highlighting the biotherapy use benefits. Conclusions: Best effect was obtained TBBA7x3days, both for clinical and parasitological parameters. It’s possible to speculate that in this regimen, biotherapy was able to modulate, more effectively, the host’s immune system, decreasing the number of parasites.