Intracerebroventricular streptozotocin (ICV-STZ) injection is among the best animal models to simulate sporadic Alzheimer disease (AD) (Hoyer, 2002, 2000, 1998; Salkovic-Petrisic and Hoyer, 2007). Brain insulin signaling abnormality (Grunblatt et al., 2007), neurodegeneration (Kamat, 2015), neuroinflammation (Liu et al., 2022), cholinergic damage (Blokland and Jolles, 1993; Roy et al., 2021), mitochondrial dysfunction (C. Correia et al., 2013), genetic abnormality (Chen et al., 2012), respiratory problem (Ebel et al., 2017), oxidative stress (Sharma and Gupta, 2001), gliosis (Rostami et al., 2017), sleep disturbances (Song et al., 2018) associated with cognitive abnormalities seen in ICV-STZ injected rats. Available experimental evidences has used varying doses of STZ (<1 to 3mg/kg) and studied its effect for different study durations, ranging from 14-21 (short), 30-42 (mild), 90-105 (moderate) and 250-270 (long) days (Chen et al., 2013, 2012; Grunblatt et al., 2007; Knezovic et al., 2015; Kraska et al., 2012; Mehla et al., 2013; Rostami et al., 2017; Salkovic-Petrisic et al., 2006). These studies indicated that 3mg/kg of body weight is the optimum dose for inducing sporadic AD in the rodents. However studies on the pathological process with relating the morphological and functional abnormalities reported were illusive. Therefore in the present study, we have investigated the effect of 3mg/kg ICV-STZ on three cognitive domains viz. spatial, episodic and avoidance and even neuropsychiatric abnormality i.e. anxiety with extensive morphological examination in the layers associated with hippocampus proper. Further, we have observed the onset of diffuse amyloid plaques, in association with enlargement of lateral ventricles and down scaling of spines in granular cells of dentate gyrus. Finally, to dissect the functional changes in spatial and anxiety variables we had examined the probability of fraction of time spent in Morris water maze and changes in ethological patterns of STZ injected rats in elevated plus maze.