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1.
Dev Psychobiol ; 66(1): e22447, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38131239

ABSTRACT

Adolescence is one of the most critical periods for brain development, and exposure to morphine during this period can have long-life effects on pain-related behaviors. The opioid system in the periaqueductal gray (PAG) is highly vulnerable to drug exposure. However, the impact of adolescent morphine exposure (AME) on the endogenous opioid system in the PAG is currently unknown. This study aims to investigate the long-lasting effects of AME on the endogenous opioid system and its involvement in altering nociceptive behaviors. Adolescent rats were given escalating doses of morphine (2.5-25 mg/kg, subcutaneous) or an equal volume of saline twice daily for 10 consecutive days (PND 31-40). After a 30-day washout period, adult rats underwent formalin tests following microinjection of morphine, naloxone, or saline into the ventrolateral PAG (vlPAG) region. The results indicated that morphine microinjection into the vlPAG of the adolescent morphine-treated group significantly reduced the nociceptive score. However, the analgesic response to morphine in this group was significantly lower compared to the saline-treated group during adolescence. Additionally, the nociceptive score significantly increased following naloxone but not saline microinjection into the vlPAG of the saline-treated group during adolescence, rather than the morphine-treated one. These findings indicate that AME has long-lasting effects on the endogenous opioid system in the vlPAG, which can consequently alter behaviors related to inflammatory pain in adulthood.


Subject(s)
Analgesics, Opioid , Morphine , Rats , Animals , Analgesics, Opioid/pharmacology , Morphine/pharmacology , Rats, Sprague-Dawley , Pain , Naloxone/pharmacology , Naloxone/therapeutic use
2.
Medicine (Baltimore) ; 103(25): e38542, 2024 Jun 21.
Article in English | MEDLINE | ID: mdl-38905413

ABSTRACT

RATIONALE: Fahr syndrome is a rare, degenerative neurological condition characterized by bilateral idiopathic calcification of the periventricular region, especially the basal ganglia. This condition is often misdiagnosed as other neurological or psychiatric disorders due to its rarity and overlapping symptoms. PATIENT CONCERNS: A 34-year-old man had been experiencing seizures and cognitive dysfunction for few years, which were further compounded by slurred speech and motor difficulties as acute conditions. DIAGNOSIS: After investigations, severe hypocalcemia, and hypoparathyroidism were detected and his brain computed tomography showed extensive bilateral calcifications in basal ganglia, thalamus, dentate nuclei, and some parts of subcortical white matter, suggestive of Fahr syndrome. Although, the patient was initially misdiagnosed due to a lack of information and the rarity of this disease. INTERVENTION: The patient was treated with intravenous calcium gluconate, vitamin D3, l-ornithine l-aspartate syrup, and levetiracetam, replacing carbamazepine. OUTCOME: His symptoms, including slurred speech, muscle pain, and stiffness improved, serum calcium normalized, and he was discharged with medications for memory deficit and depression. LESSONS: This case underscores the importance of raising awareness among physicians, especially in areas with limited medical resources, about the significance of prompt diagnosis and appropriate symptomatic treatment in enhancing patient prognosis and quality of life.


Subject(s)
Calcinosis , Cognitive Dysfunction , Seizures , Humans , Male , Adult , Seizures/etiology , Seizures/drug therapy , Cognitive Dysfunction/etiology , Cognitive Dysfunction/diagnosis , Calcinosis/complications , Calcinosis/diagnosis , Afghanistan , Basal Ganglia Diseases/diagnosis , Basal Ganglia Diseases/complications , Hypoparathyroidism/complications , Hypoparathyroidism/diagnosis , Hypoparathyroidism/drug therapy , Hypocalcemia/drug therapy , Tomography, X-Ray Computed , Neurodegenerative Diseases
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