Is each horse unique and unrepeatable? An explanation through morphometric and statistical analysis of the limb bones.

Horses went through functional differentiation during their evolutionary and reproductive development, however, some body parts continued to improve their specificity for speed. Regarding this, we evaluated by morphometric analysis the relationship between limb section (LS) differences in the appendicular structures of horses. Two hundred and seven (n = 207) adult horses of different breeds and sex were selected. The limb section was measured by identification of topographic palpable skeleton landmarks with a measurement tape (centimetres). Quantitative variables (limb section) were analysed with PAST Paleontological Statistics Version 3.16. Spearman's ordinal or non-parametric correlation coefficient was used to study the relationship between the limb section of each variable (p < 0.05), with a low coefficient of variation (<30%). In 45 analysed correlations, 35 were statistically significant and 10 were discarded because p > 0.05. These results show that most variables were correlated with each other. As a result, we can imply that some LS of the horse's limbs are correlated with each other, positively or negatively and to a different degree. In conclusion, the correlations between LS lengths determine the size and shape of each horse, making individual horses unique and unrepeatable.

A Comprehensive Analysis of Replicative Lifespan in 4,698 Single-Gene Deletion Strains Uncovers Conserved Mechanisms of Aging.

Many genes that affect replicative lifespan (RLS) in the budding yeast Saccharomyces cerevisiae also affect aging in other organisms such as C. elegans and M. musculus. We performed a systematic analysis of yeast RLS in a set of 4,698 viable single-gene deletion strains. Multiple functional gene clusters were identified, and full genome-to-genome comparison demonstrated a significant conservation in longevity pathways between yeast and C. elegans. Among the mechanisms of aging identified, deletion of tRNA exporter LOS1 robustly extended lifespan. Dietary restriction (DR) and inhibition of mechanistic Target of Rapamycin (mTOR) exclude Los1 from the nucleus in a Rad53-dependent manner. Moreover, lifespan extension from deletion of LOS1 is nonadditive with DR or mTOR inhibition, and results in Gcn4 transcription factor activation. Thus, the DNA damage response and mTOR converge on Los1-mediated nuclear tRNA export to regulate Gcn4 activity and aging.

Molecular mechanisms underlying genotype-dependent responses to dietary restriction.

Dietary restriction (DR) increases lifespan and attenuates age-related phenotypes in many organisms; however, the effect of DR on longevity of individuals in genetically heterogeneous populations is not well characterized. Here, we describe a large-scale effort to define molecular mechanisms that underlie genotype-specific responses to DR. The effect of DR on lifespan was determined for 166 single gene deletion strains in Saccharomyces cerevisiae. Resulting changes in mean lifespan ranged from a reduction of 79% to an increase of 103%. Vacuolar pH homeostasis, superoxide dismutase activity, and mitochondrial proteostasis were found to be strong determinants of the response to DR. Proteomic analysis of cells deficient in prohibitins revealed induction of a mitochondrial unfolded protein response (mtUPR), which has not previously been described in yeast. Mitochondrial proteotoxic stress in prohibitin mutants was suppressed by DR via reduced cytoplasmic mRNA translation. A similar relationship between prohibitins, the mtUPR, and longevity was also observed in Caenorhabditis elegans. These observations define conserved molecular processes that underlie genotype-dependent effects of DR that may be important modulators of DR in higher organisms.

Digestive peritoneum in Wistar rat (Rattus norvegicus) / Peritoneo del aparato digestivo de la rata Wistar (Rattus norvegicus)

La rata de laboratorio (Rattus norvegicus albinus) ha sido usada como modelo para investigaciones médicas, biológicas y moleculares, desde hace mucho tiempo. Sin embargo, no existen descripciones detalladas del peritoneo digestivo de la rata wistar. El objetivo de este trabajo es definir en forma clara y acorde a los principios de la Nómina Anatómica Veterinaria el peritoneo en esta especie de mamífero de laboratorio. Se utilizaron ochenta y ocho ratas (Rattus norvegicus albinus) de entre 250 y 450 g. Fueron disecadas en fresco luego de ser eutanasiadas por sobredosis de tiopental sódico intraperitoneal. Se realizó una incisión paramediana que se extendía desde el cartílago xifoides del esternón hasta el pubis y otra sobre cada arco costal hacia dorsal.

The laboratory rat (Rattus norvegicus albinus) has been used as a model for medical, biological and molecular research, for a long time. It is an interesting fact that there are no detailed descriptions of the gross anatomy of the liver and its ways of fixation. The aim of this study is to define clearly and according to the Nomina Anatomica Veterinaria principles, the liver and its way of fixation in this species of laboratory mammal. Eighty-eight rats (Rattus norvegicus albinus) were used, with a weight between 250 and 450 g. They were dissected in fresh, after been euthanized by an overdose of thiopental sodium intraperitoneal. An incision from the xiphoid cartilage up to the pubic region was made and another on each costal arch toward dorsal.

End-of-life cell cycle arrest contributes to stochasticity of yeast replicative aging.

There is growing evidence that stochastic events play an important role in determining individual longevity. Studies in model organisms have demonstrated that genetically identical populations maintained under apparently equivalent environmental conditions display individual variation in life span that can be modeled by the Gompertz-Makeham law of mortality. Here, we report that within genetically identical haploid and diploid wild-type populations, shorter-lived cells tend to arrest in a budded state, while cells that arrest in an unbudded state are significantly longer-lived. This relationship is particularly notable in diploid BY4743 cells, where mother cells that arrest in a budded state have a shorter mean life span (25.6 vs. 35.6) and larger coefficient of variance with respect to individual life span (0.42 vs. 0.32) than cells that arrest in an unbudded state. Mutations that cause genomic instability tend to shorten life span and increase the proportion of the population that arrest in a budded state. These observations suggest that randomly occurring damage may contribute to stochasticity during replicative aging by causing a subset of the population to terminally arrest prematurely in the S or G2 phase of the cell cycle.

Dietary restriction and mitochondrial function link replicative and chronological aging in Saccharomyces cerevisiae.

Chronological aging of budding yeast cells results in a reduction in subsequent replicative life span through unknown mechanisms. Here we show that dietary restriction during chronological aging delays the reduction in subsequent replicative life span up to at least 23days of chronological age. We further show that among the viable portion of the control population aged 26days, individual cells with the lowest mitochondrial membrane potential have the longest subsequent replicative lifespan. These observations demonstrate that dietary restriction modulates a common molecular mechanism linking chronological and replicative aging in yeast and indicate a critical role for mitochondrial function in this process.

pH neutralization protects against reduction in replicative lifespan following chronological aging in yeast.

Chronological and replicative aging have been studied in yeast as alternative paradigms for post-mitotic and mitotic aging, respectively. It has been known for more than a decade that cells of the S288C background aged chronologically in rich medium have reduced replicative lifespan relative to chronologically young cells. Here we report replication of this observation in the diploid BY4743 strain background. We further show that the reduction in replicative lifespan from chronological aging is accelerated when cells are chronologically aged under standard conditions in synthetic complete medium rather than rich medium. The loss of replicative potential with chronological age is attenuated by buffering the pH of the chronological aging medium to 6.0, an intervention that we have previously shown can extend chronological lifespan. These data demonstrate that extracellular acidification of the culture medium can cause intracellular damage in the chronologically aging population that is asymmetrically segregated by the mother cell to limit subsequent replicative lifespan.

Caffeine extends life span, improves healthspan, and delays age-associated pathology in Caenorhabditis elegans.

BACKGROUND: The longevity of an organism is influenced by both genetic and environmental factors. With respect to genetic factors, a significant effort is being made to identify pharmacological agents that extend life span by targeting pathways with a defined role in the aging process. On the environmental side, the molecular mechanisms responsible for the positive influence of interventions such as dietary restriction are being explored. The environment experienced by humans in modern societies already contains countless compounds that may influence longevity. Understanding the role played by common compounds that substantially affect the aging process will be critical for predicting and interpreting the outcome of introducing new interventions. Caffeine is the most widely used psychoactive drug worldwide. Prior studies in flies, worms, and mice indicate that caffeine may positively impact age-associated neurodegenerative pathology, such as that observed in Alzheimer's disease. RESULTS: Here we report that caffeine is capable of extending life span and improving healthspan in Caenorhabditis elegans, a finding that is in agreement with a recently published screen looking for FDA-approved compounds capable of extending worm life span. Life span extension using caffeine displays epistatic interaction with two known longevity interventions: dietary restriction and reduced insulin signaling. Caffeine treatment also delays pathology in a nematode model of polyglutamine disease. CONCLUSIONS: The identification of caffeine as a relevant factor in aging and healthspan in worms, combined with prior work in both humans and rodents linking caffeine consumption to reduced risk of age-associated disease, suggests that caffeine may target conserved longevity pathways. Further, it may be important to consider caffeine consumption when developing clinical interventions, particularly those designed to mimic dietary restriction or modulate insulin/IGF-1-like signaling. The positive impact of caffeine on a worm model of polyglutamine disease suggests that chronic caffeine consumption may generally enhance resistance to proteotoxic stress and may be relevant to assessing risk and developing treatments for human diseases like Alzheimer's and Huntington's disease. Future work addressing the relevant targets of caffeine in models of aging and healthspan will help to clarify the underlying mechanisms and potentially identify new molecular targets for disease intervention.

Sir2 deletion prevents lifespan extension in 32 long-lived mutants.

Activation of Sir2 orthologs is proposed to increase lifespan downstream of dietary restriction. Here, we describe an examination of the effect of 32 different lifespan-extending mutations and four methods of DR on replicative lifespan (RLS) in the short-lived sir2Δ yeast strain. In every case, deletion of SIR2 prevented RLS extension; however, RLS extension was restored when both SIR2 and FOB1 were deleted in several cases, demonstrating that SIR2 is not directly required for RLS extension. These findings indicate that suppression of the sir2Δ lifespan defect is a rare phenotype among longevity interventions and suggest that sir2Δ cells senesce rapidly by a mechanism distinct from that of wild-type cells. They also demonstrate that failure to observe lifespan extension in a short-lived background, such as cells or animals lacking sirtuins, should be interpreted with caution.

Anatomía del peritoneo digestivo del ñandú (Rhea americana) / Digestive peritoneum anatomy of the Rhea (Rhea americana)

El ñandú (Rhea americana) es un ave corredora autóctona de Sudamérica la cual hace ya algunos años ha despertado cierto interés productivo. Sin embargo, la morfología detallada a nivel de las aves domésticas aún se desconoce en muchos aspectos; entre ellos el peritoneo. El objetivo de este trabajo es describir el peritoneo parietal, visceral y de conexión del ñandú acorde con los principios de la Nómina Anatómica Aviar. Se utilizaron 7 animales adultos; 5 machos y 2 hembras de entre 8 y 25 kg. de peso procedentes de un criadero comercial. Fueron eutanasiados por sobredosis de tiopental sódico. La cavidad peritoneal estaba dividida en una parte craneal (equivalente a 1/3) y una parte caudal al estómago (equivalente a 2/3 del total del abdomen). En la parte caudal se encontraba la totalidad del intestino y el páncreas, mientras que en la parte craneal se observó el hígado y la vesícula biliar. Un omento menor fijaba el estómago al hígado cranealmente hacia la derecha y un omento mayor pequeño con una bolsa omental cerrada lo fijaba caudalmente hacia la izquierda. La raíz del mesenterio fijaba al yeyuno, al íleon y a ambos ciegos entre sus hojas a través de amplios pliegues ileocecales. Desde la raíz del mesenterio un corto mesoduodeno sujetaba al duodeno descendente y ascendente hacia la derecha. El colon estaba sostenido por un amplio mesocolon desde distal a la desembocadura de los ciegos hasta su terminación en la cloaca. Se concluye que esta especie corredora presenta similitudes con las aves domésticas. Sin embargo, lo relativamente grueso y fuerte del peritoneo de conexión sumado a lo compartimentado de la cavidad peritoneal hacen suponer que se trata de una adaptación para la carrera al permitir una gran sujeción de las vísceras abdominales.

The rhea (Rhea americana) is a native ratite from South America which has woken up since a few years ago a big productive interest. However the detailed morphology of the rhea at the level at the domestic birds is still unknown in many aspects, on of them is the peritoneum. The aim of this work is to describe the parietal, visceral and connection peritoneum of the rhea according to the anatomical avian nomenclature. Seven specimens of adult rhea were used, five males and two females about 8 and 25 kg of weight. All of them proceeding from a commercial farm. The animals were slaughtered before their study. The peritoneum that cover the abdominal wall and the visceral and connection peritoneum that support the abdominal viscera were observed and described. The peritoneal cavity were divided into two parts, one was craneal to the ventriculum (1/3 parts from the total of the abdomen) and the other was caudal (2/3). Into the cranial part we founded the liver and the gallbladder while into the caudal part we founded the intestine and the pancreas. The stomach was fixed to the liver cranially to the right by a minor omentus and caudally to the left was fixed by a small major omentus with a close omental bag. The root of the mesentery was fixing the yeyuno, ileum and both caecums between its sheets towards wide ileocecalis creases. From the mesentery root a short mesoduodenum was holding the descending and ascending duodenum towards the right. The colon was supported by a wide mesocolon. We concluded that this ratite has similarities with the domestic birds. Nevertheless, the thickness and strong connection peritoneum and the compartmentalization of the peritoneal cavity make us suppose that it is an adaption to the race since it is a big subjection to the abdominal viscera.