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Stress may cause or aggravate Bladder Pain Syndrome/Interstitial Cystitis (BPS/IC) symptoms. Thus, stress models are being refined to be used as systemic in counterpoint to bladder centric animal models We hypothesised that different stress insults modulate the insula activity diversely. Two models were used in female Wistar rats, Maternal Deprivation Model (MDM, stress applied to new-borns and studies done at 6M) and Water Avoidance Stress test (WAS, stress is applied to 6M rats for 1h every 10 days and studies carried afterwards). Mechanical pain threshold was evaluated in L6/S1 dermatomes which share the spinal cord segments of bladder sensory innervation. Bladder function was evaluated by cystometry. Then Insulas were removed. One was immersed in RNAlater, homogenized, RNA extracted, and expression of different biomarkers assessed by real-time PCR. The other insula was immunoreacted against microglia markers Iba1 and Cd68. The analysis of positive cells used LASAF and ImageJ software. Morphometric analysis and 3D reconstructions used IMARIS software.

Microglia have been increasingly implicated in neurodegenerative diseases (NDs), and specific disease associated microglia (DAM) profiles have been defined for several of these NDs. Yet, the microglial profile in Machado–Joseph disease (MJD) remains unexplored. Here, we characterized the profile of microglia in the CMVMJD135 mouse model of MJD. This characterization was performed using primary microglial cultures and microglial cells obtained from disease-relevant brain regions of neonatal and adult CMVMJD135 mice, respectively. Machine learning models were implemented to identify potential clusters of microglia based on their morphological features, and an RNA-sequencing analysis was performed to identify molecular perturbations and potential therapeutic targets. Our findings reveal morphological alterations that point to an increased activation state of microglia in CMVMJD135 mice and a disease-specific transcriptional profile of MJD microglia, encompassing a total of 101 differentially expressed genes, with enrichment in molecular pathways related to oxidative stress, immune response, cell proliferation, cell death, and lipid metabolism. Overall, these results allowed us to define the cellular and molecular profile of MJD-associated microglia and to identify genes and pathways that might represent potential therapeutic targets for this disorder., This work was supported by Fundação para a Ciência e a Tecnologia (FCT) (PTDC/NEUNMC/3648/2014) and COMPETE-FEDER (POCI-01-0145-FEDER-016818). It was also supported by Portuguese funds through FCT in the framework of the Project POCI-01-0145-FEDER-031987 (PTDC/MED-OUT/31987/2017). A.B.C. was supported by a doctoral fellowship from FCT (PD/BD/ 127828/2016). S.P.N. was also supported by FCT (PD/BD/114120/2015). Work in the JBR laboratory was financed by FEDER—Fundo Europeu de Desenvolvimento Regional funds through the COMPETE 2020—Operational Programme for Competitiveness and Internationalization (POCI), Portugal 2020, and by Portuguese funds through FCT in the framework of the Project POCI-01-0145- FEDER030647 (PTDC/MED-NEU/31318/2017). This work was funded by ICVS Scientific Microscopy Platform, member of the national infrastructure PPBI (Portuguese Platform of Bioimaging) (PPBIPOCI-01-0145-FEDER-022122), and by National funds, through FCT—project UIDB/50026/2020 and UIDP/50026/2020.

Retrato de Maria de Sousa - Maria de Sousa e a luminosidade do esperado ��� por Teresa Summavielle, sobre a Professora Catedr��tica no Instituto de Ci��ncias Biom��dicas de Abel Salazar e investigadora, defensora de uma Ci��ncia integrada na Universidade, aspirando construir um pa��s respeitado pela pr��tica da Ci��ncia e pela proje����o internacional dos seus cientistas., Summavielle, T. (2021). Maria de Sousa e a luminosidade do esperado. Faces de Eva. Estudos sobre a Mulher, (45), 199-204. ISSN: 0874-6885

Exposure to cocaine in early periods of postnatal life is usually associated with changes in development of neurotransmitter systems and structure of the central nervous system. Such changes are most likely correlated with behavioral alterations. Environmental enrichment conditions (EC) in early stages is a factor that affects structural and behavioral development. The purpose of this study is to examine the effects of EC on rats postnatally exposed to cocaine on exploratory behavior. Wistar rats were as signed to four groups—Group 1: pups exposed to cocaine hydrochloride (15 mg/kg body weight/day) s.c., in two daily doses, from postnatal day (PND) 1 to 28 and reared in EC; Group 2: pups exposed to cocaine as previously described and reared in a stan dard environmental conditions (SC); Group 3: pups saline-injected and reared in EC; and Group 4: pups saline-injected and reared in SC. On PND 21, 24, and 28, groups of four rats (to reduce anxiety) were placed for 10 minutes into an arena with sev eral objects. The following exploratory behavioral categories were examined: object interaction, exploration, manipulation, approximation, and total time of object contact. Animals from Group 2 showed decreased object interaction and total contact on PND 21. Control offspring reared in EE showed decreases in exploratory behavior at all ages analyzed compared with the control SE group, while cocaine-exposed animals reared in EC showed decreased object interaction, object approximation, and total exploratory behavior. The results in this group suggest that EC improved information acquisition and memory processes in animals postnatally exposed to cocaine.

The use of cocaine in adults has been linked to depression and/or anxiety. Several studies have shown an association between cocaine-primed craving and depressive symptoms. In animal models, the forced swim test (FST) is frequently used for screening depressive-like behavior. This study aimed to verify the presence of depression-like symptoms in adolescent rats after chronic cocaine exposure by analyzing behavior in a FST. The subsequent alterations in neurotransmitters and hypothalamus-pituitary-adrenal axis activity induced by this test were also analyzed. Both male and female adolescent Wistar rats were submitted to a chronic “binge” pattern of administration of cocaine hydrochloride, and subjects were tested in a forced swim test 2 days after cocaine's last administration. At the end of the behavioral test, trunk blood was collected for quantification of corticosterone plasma levels, and hypothalamus, prefrontal cortex, amygdala, and hippocampus were dissected for neurochemical determinations. No significant differences were found in the behavior on the FST of both males and females after withdrawal from chronic cocaine administration. Nevertheless, plasma levels of corticosterone were increased in cocaine-treated males, although not significantly (P= 0.065). In females cocaine failed to affect corticosterone levels. Of interest, neurochemical analyses showed that dopamine turnover was decreased in amygdala in cocaine-treated males (not significantly, P= 0.055). No significant differences were found on neurotransmitter levels in the other brain regions analyzed. Withdrawal from chronic cocaine administration during adolescence did not have a significant effect on stress-induced behavioral alterations, although the neurochemical response to the stressful situation provided by FTS seemed to be affected.

Exposure to cocaine throughout gestation may produce several deleterious outcomes in the offspring that include effects on neurotransmitter systems and structure of the central nervous system. Such changes are most likely correlated with behavioral alterations. Environmental enrichment (EE) in early stages is a factor that affects structural and behavioral development. This article examines the effects, upon social interactions, of EE during the first month of life in rats prenatally exposed to cocaine. Wistar dams were subcutaneously exposed to 60 mg/kg of cocaine divided in two daily doses from gestational day (GD)8 to GD22. Pair-fed controls were given saline vehicle in the same protocol. Offspring were distributed to the different environments in four experimental groups. Group 1: offspring from dams prenatally exposed to cocaine as previously described and reared in EE from postnatal day (PND)1 to PND28; Group 2: pups from cocaine-exposed dams and reared in a standard environment (SE); Group 3: pups from pair-fed saline-exposed dams and reared in EE; Group 4: offspring from saline-exposed dams and reared in SE. On PND21, 24, and 28, rats were examined in several social behavioral categories (play fighting, social investigation, comfort behaviors, and solicitation to play) for 10 min. Animals reared in SE do not display any differences due to treatment in the behavioral categories analyzed. Control offspring reared in EE presented decreased play fighting, decreased solicitation to play, and decreased social investigation compared to the control SE group, while cocaine-exposed animals reared in EE did not present these variations. These results suggest that EE rearing may unmask hidden effects of prenatal cocaine exposure.

Radioimmunoassay (RIA) was applied to identify selected metabolites obtained in in vitro incubations of ovarian and hepatopancreatic tissues from female Marsupenaeus japonicus in previtellogenic and vitellogenic maturation stages. Depending on the precursors used, progesterone, 17?-hydroxyprogesterone or testosterone, it was possible to observe the presence of several enzymatic activities through metabolites detected in incubations. The present study provides evidence that the ovary of the shrimp M. japonicus is capable of synthesising 17?-estradiol from progesterone, evidencing the presence of 17?-hydroxylase, C17-C20 lyase, 17?-hydroxysteroid dehydrogenase (17?-HSD) and aromatase. Enzymatic activities of aromatase, 3?-HSD and 17?-hydroxylase were detected in hepatopancreas, but not that of C17-C20 lyase. These results suggest that 17?-estradiol could be the vitellogenesis stimulating ovarian hormone (VSOH), and together with former in vivo and in vitro studies this leads us to propose that in fact there may be a physiological role for steroid hormones in the maturation cycle of crustaceans., Se utilizó el radioinmunoensayo (RIA) para identificar los metabolitos seleccionados obtenidos en incubaciones in vitro del ovario y del hepatopáncreas de hembras en estado de maduración previtelogénico y vitelogénico de Marsupenaeus japonicus. Dependiendo del precursor utilizado: progesterona, 17?-hidroxiprogesterona o testosterona fue posible observar la presencia de diversas actividades enzimáticas a través de metabolitos detectados en las incubaciones. El presente estudio demuestra que el ovario del langostino M. japonicus es capaz de sintetizar 17?-estradiol a partir de progesterona y pone en evidencia la presencia de 17?-hidroxilasa, C17-C20liasa, 17?-hidroxiesteroide deshidrogenasa (17-HSD) y aromatasa. La actividad enzimática de la aromatasa, 3?-HSD y 17?-hidroxilasa se detectó en el hepatopáncreas, pero de C17-C20liasa. Estos resultados sugieren que el 17?-estradiol podría ser la hormona estimuladora de la vitelogénesis (VSOH), y conjuntamente con anteriores estudios in vivo e in vitro nos dirige a proponer que de hecho debería existir una función fisiológica para las hormonas esteroides en el ciclo de maduración de los crustáceos.