Dataset on assessing olfactory function in the residents of Central Russia using the University of Pennsylvania Smell Identification Test.

Data were acquired via sensory testing of olfactory function in 252 adult residents of Central Russia (18-87 years old), including groups from urban and rural areas. The 40-item North American version of the University of Pennsylvania Smell Identification Test (UPSIT) was used. The test alternatives were initially translated into Russian by the authors with minor adaptations. We followed the test procedure recommended by the manufacturer and introduced additional tasks. Familiarity with odor names and consistency with the pre-existing concepts for the test odor items were determined using multiple response questions. Intensity ratings for the UPSIT odorants were obtained using 4-point categorical scale for a subset of the participants. Demographic data and other relevant characteristics of the study population were collected using an adapted translation of the questionnaire included with the test. Descriptive statistics of the collected data are presented in this article. The dataset may be reused for evaluating the impact of various factors, such as cultural context, age, sex, environment, and smoking habits, on the perception of specific odorants as well as on general olfactory function (determined by the number of recognized test items). The data may find its application in the clinical practice of otolaryngologists and neurologists who work with the ethno-cultural group in Russia and all over the world. The dataset can also be used for development of new diagnostic tools for olfactory dysfunction.

Olfactory perception of 5α-androst-16-en-3-one: Data obtained in the residents of central Russia.

This dataset describes olfactory perception of androstenone (5α-androst-16-en-3-one) in residents of central Russia (n=807, 9-84 years old). Based on previous studies, 3.13 × 10-3% androstenone was utilized for sensory testing. A modified two-alternative choice task with "no-difference" options was applied as an odor discrimination procedure. The participants rated the perceived odor intensity and pleasantness on 3-point categorical scales. The subsequent task was free odor identification. We used a survey to determine characteristics of our study population such as age, sex, ethnicity, olfactory abilities, smoking habits, respiratory tract diseases, perfume use, blood group. To examine sex differences in characteristics of participants, as well as in their perception of androstenone, we have applied one-way ANOVA for age variable and Chi-square tests for categorical variables. The dataset will be useful for assessing the impact of the aforementioned factors on the perception of volatile steroids. A wide range of researchers studying verbal descriptors of specific odors and cross-cultural differences in olfactory perception may reuse this dataset. Primarily, this dataset may benefit meat industry, as androstenone, which is perceived as an unpleasant odor by about a quarter of the population, significantly contributes to pork flavor.

Aerobic training reverses high-fat diet-induced pro-inflammatory signalling in rat skeletal muscle.

High-fat feeding activates components of the pro-inflammatory pathway and increases co-immunoprecipitation of suppressor of cytokine signalling (SOCS)-3 with both the insulin receptor (IR)-ß subunit and IRS-1, which together contribute to keeping PI-3 kinase from being fully activated. However, whether aerobic training reverses these impairments is unknown. Sprague-Dawley rats were fed a chow (CON, n = 8) or saturated high-fat (n = 16) diets for 4 weeks. High-fat-fed rats were then allocated (n = 8/group) to either sedentary (HF) or aerobic exercise training (HFX) for an additional 4 weeks after which all animals underwent hind limb perfusions. Insulin-stimulated red quadriceps 3-O-methylglucose transport rates and PI-3 kinase activity were greater (p < 0.05) in CON and HFX compared to HF. IRS-1 tyrosine phosphorylation was increased (p < 0.05) and IRS-1 serine 307 phosphorylation was decreased (p < 0.05) in HFX compared to HF. IR-ß subunit co-immunoprecipitation with IRS-1 was increased in HFX compared to HF. SOCS-3 co-immunoprecipitation with both the IR-ß subunit and IRS-1 was decreased (p < 0.05) in HFX compared to HF. IKKα/ß serine phosphorylation, and IκBα serine phosphorylation were decreased (p < 0.05) while IκBα protein concentration was increased in HFX compared to HF. By decreasing the association of SOCS-3 with both the IR-ß subunit and IRS-1 the interaction between IRS-1 and the IR-ß subunit was normalized in the HFX, and may have contributed to skeletal muscle PI-3 kinase being fully activated by insulin. Additionally, the reduction in IKKα/ß serine phosphorylation in HFX may have contributed to decreasing IRS-1 serine phosphorylation, and in turn, promoted the normalization of insulin-stimulated activation of PI-3 kinase.

High-fat feeding increases insulin receptor and IRS-1 coimmunoprecipitation with SOCS-3, IKKalpha/beta phosphorylation and decreases PI-3 kinase activity in muscle.

Suppressor of cytokine signaling (SOCS) proteins and/or activation of the proinflammatory pathway have been postulated as possible mechanisms that may contribute to skeletal muscle insulin resistance. Thus, the aims of the present investigation were to determine in high-fat-fed skeletal muscle: 1) whether SOCS-3 protein concentration is increased, 2) whether coimmunoprecipitation of SOCS-3 with the insulin receptor-beta subunit and/or IRS-1 is increased, and 3) whether select components of the proinflammatory pathway are altered. Thirty-two male Sprague-Dawley rats were assigned to either control (CON, n = 16) or high-fat-fed (HF, n = 16) dietary groups for 12 wk and then subjected to hind limb perfusions in the presence (n = 8/group) or absence (n = 8/group) of insulin. Insulin-stimulated skeletal muscle 3-MG transport rates and PI-3 kinase activity were greater (P < 0.05) in CON. IRS-1 tyrosine phosphorylation was decreased (P < 0.05), and IRS-1 serine 307 phosphorylation was increased (P < 0.05) in HF. Insulin receptor-beta (IR-beta) subunit coimmunoprecipitation with IRS-1 was reduced in HF. SOCS-3 protein concentration and SOCS-3 coimmunoprecipitation with both the IR-beta subunit and IRS-1 was increased (P < 0.05) in HF. IKKalpha/beta serine phosphorylation was increased (P < 0.05), IkappaBalpha protein concentration was decreased (P < 0.05) and IkappaBalpha serine phosphorylation was increased (P < 0.05) in HF. Increased colocalization of SOCS-3 with both the IR-beta subunit and IRS-1 may provide steric hindrance that prevents IRS-1 from interacting with IR-beta, while increased IKKbeta serine phosphorylation may contribute to increasing IRS-1 serine phosphorylation, both of which independently can have deleterious effects on insulin-stimulated PI-3 kinase activation in high-fat-fed rodent skeletal muscle.

Exercise reverses high-fat diet-induced impairments on compartmentalization and activation of components of the insulin-signaling cascade in skeletal muscle.

The aims of this investigation were 1) to determine whether endurance exercise training could reverse impairments in insulin-stimulated compartmentalization and/or activation of aPKCzeta/lambda and Akt2 in skeletal muscle from high-fat-fed rodents and 2) to assess whether the PPARgamma agonist rosiglitazone could reverse impairments in skeletal muscle insulin signaling typically observed after high-fat feeding. Sprague-Dawley rats were placed on chow (NORCON, n = 16) or high-fat (n = 64) diets for 4 wk. During a subsequent 4-wk experimental period, high-fat-fed rats were allocated (n = 16/group) to either sedentary control (HFC), exercise training (HFX), rosiglitazone treatment (HFRSG), or a combination of both exercise training and rosiglitazone (HFRX). Following the 4-wk experimental period, animals underwent hindlimb perfusions. Insulin-stimulated plasma membrane-associated aPKCzeta and -lambda protein concentration, aPKCzeta/lambda activity, GLUT4 protein concentration, cytosolic Akt2, and aPKCzeta/lambda activities were reduced (P < 0.05) in HFC compared with NORCON. Cytosolic Akt2, aPKCzeta, and aPKClambda protein concentrations were not affected in HFC compared with NORCON. Exercise training reversed the deleterious effects of the high-fat diet such that insulin-stimulated compartmentalization and activation of components of the insulin-signaling cascade in HFX were normalized to NORCON. High-fat diet-induced impairments to skeletal muscle glucose metabolism were not reversed by rosiglitazone administration, nor did rosiglitazone augment the effect of exercise. Our findings indicate that chronic exercise training, but not rosiglitazone, reverses high-fat diet induced impairments in compartmentalization and activation of components of the insulin-signaling cascade in skeletal muscle.