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In particular, NCX2 positive synaptic terminals were increased in AD cohort while the number of NCX3 positive terminals were reduced. In addition, NCX1, NCX2 and NCX3 isoforms were up-regulated in those synaptic terminals accumulating amyloid-beta (Aβ), the neurotoxic peptide responsible for AD neurodegeneration. More recently, the hyperfunction of a specific NCX subtype, NCX3, has been shown to delay endoplasmic reticulum stress and apoptotic neuronal death in hippocampal neurons exposed to Aβ insult. Despite some issues about the functional role of NCX in synaptic failure and neuronal loss require further studies, these findings highlight the putative neuroprotective role of NCX in AD and open new strategies to develop new druggable targets for AD therapy. Since the discovery of the three isoforms of the Na+/Ca2+ exchanger, NCX1, NCX2 and NCX3 in 1990s, many studies have been devoted to identifying their specific roles in different tissues under several physiological or pathophysiological conditions. In particular, several seminal experimental works laid the foundation for better understanding gene and protein structures, tissue distribution, and regulatory functions of each antiporter isoform. On the other hand, despite the efforts in the development of specific compounds selectively targeting NCX1, NCX2 or NCX3 to test their physiological or pathophysiological roles, several drawbacks hampered the achievement of these goals. In fact, at present no isoform-specific compounds have been yet identified. Moreover, these compounds, despite their potency, possess some nonspecific actions against other ion antiporters, ion channels, and channel receptors. As a result, it is difficult to discriminate direct effects of inhibition/activation of NCX isoforms from the inhibitory or stimulatory effects exerted on other antiporters, channels, receptors, or enzymes. To overcome these difficulties, some research groups used transgenic, knock-out and knock-in mice for NCX isoforms as the most straightforward and fruitful strategy to characterize the biological role exerted by each antiporter isoform. The present review will survey the techniques used to study the roles of NCXs and the current knowledge obtained from these genetic modified mice focusing on the advantages obtained with these strategies in understanding the contribution exerted by each isoform. AIMS/BACKGROUND People diagnosed with multiple drug use disorders are high-risk subpopulations, but changes in diagnostic classification and drug use prevalence mean patterning of drug use disorders has changed in the past decade. We analyzed comorbidity patterns of lifetime drug use disorder in a general population sample. DESIGN Using latent class analysis, we derived lifetime drug use disorder classes based on dichotomous indicators of sedative, cannabis, opioid, cocaine, stimulant, hallucinogen, inhalant/solvent, club drug, heroin, and other drug use disorders in the National Epidemiologic Survey on Alcohol and Related Conditions-III (n = 36,309). Multinomial models assessed associations between sociodemographic and clinical correlates and latent class status. RESULTS Four latent classes of lifetime substance use disorder were identified A very low risk class, a class with high opioid, sedative and heroin comorbidity, a class based on cocaine and stimulant comorbidity, and class with high likelihood of multiple lifetime drug use disorders. All higher risk classes were associated with higher risk of lifetime personality disorder and mood disorder. Conduct disorder was also associated with higher risk, but level of risk varied by class. Opioid and sedative class was associated with higher odds of lifetime eating disorder diagnosis. CONCLUSIONS Comorbidity of drug use disorders is associated with a range of lifetime mental health disorder diagnoses. Unlike previous research, we did not identify a cannabis use class, possibly due to changes in diagnostic criteria and cannabis prevalence rates. Semiconducting frameworks possessing porous structure are promising platforms for the detection of hazardous gas molecules. In this study, we propose a facile route to fabricate millimeter-scale, three-dimensional semiconducting SWCNT (s-SWCNT) aerogels and demonstrate deactivation of the co-existing metallic SWCNT (m-SWCNT) network via electrical breakdown process. In particular, the on-off ratio of the modulated semiconducting aerogel after the electrical breakdown process was 205, which is an increase of 18.9 times over that before the process. The modulated semiconducting SWCNT aerogels with a large specific surface area (∼1270 m2 g-1) demonstrated their applicability for highly sensitive ppb-level ozone detection. The modulated semiconducting networks led to a 1310 % increase in the magnitude of response to 30-ppb ozone gas injection compared with that of pristine SWCNT aerogels. Furthermore, the prepared aerogels could detect 3 ppb of ozone within 40 s and retain stable reversible ozone detection for 200 cyclic operations over 100 h. Thus, the proposed semiconducting SWCNT aerogels are a promising candidate for highly sensitive environmental gas sensors. selleck products Microplastics pollution has become a global concern in recent years. In this work, the potential influences of polyethylene (PE) microplastics on the residue, degradation and distribution behaviors of eight pesticides (epoxiconazole, tebuconazole, myclobutanil, azoxystrobin, simazine, terbuthylazine, atrazine and metolachlor) in the aquatic environment were investigated. The results showed that the presence of 2-50 g L-1 microplastics could decrease the pesticide residues in water. The adsorption isotherms were linear, indicating the process was dominated by partitioning into the bulk polymer. The desorption kinetics data implied the desorption process obeyed a pseudo-second-order kinetic model, with R2 above 0.99 in most cases. Aging treatment of microplastics had no significant effects on the interaction with the pesticides. The presence of PE microplastics could significantly prolong the degradation half-lives of pesticides in water, especially for those with moderate degradation half-lives and high log Kow values.