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Cefazolin

Manufactured by Reckitt Benckiser
Sourced in United Kingdom

Cefazolin is a prescription antibiotic medication that belongs to the cephalosporin class of antibiotics. It is used to treat a variety of bacterial infections. Cefazolin works by interfering with the bacterial cell wall formation, which leads to the death of the bacteria.

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5 protocols using cefazolin

1

Spinal Cord Transection Animal Model

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Two SCI animal models were used. Because TH+ neurons were observed throughout the length of the spinal cord, we transected the spinal cord at the higher thoracic level (T4) to study injury-induced intraspinal plasticity, as a high level of injury affects a substantial amount of spinal cord tissue below the injury. To evaluate bladder function, however, we performed T10-transection to complete remove supraspinal control and partially remove some propriospinal projections onto spinal micturition neuronal circuits as descending propriospinal projections may affect bladder function following SCI. Animals were anesthetized with 2% isoflurane. A partial laminectomy was performed at T3 or T9 vertebra to expose the dorsal spinal cord. The spinal cord was completely transected at T4 (T4–Tx; n = 18) or at T10 (T10–Tx; n = 52) using a No.11 blade. Lesion completeness was verified visually at the time of surgery and histologically following perfusion. Overlying musculature and skin were then closed. Animals were administered Lactated Ringer’s solution (Baxter Healthcare, Deerfield, IL), cefazolin (10 mg/kg), and buprenex (0.1 mg/kg; Reckitt Benckiser) post-operatively. Bladders were manually expressed at least twice daily until sacrifice.
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2

Spinal Cord Transection in Rats

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Rats underwent a complete spinal cord transection at the 10th thoracic level (T10) to remove supraspinal control of micturition. Animals were anesthetized with 2% isoflurane and a partial laminectomy was performed at the T8 vertebrae to expose the dorsal spinal cord. The spinal cord was completely transected at T10 using a No. 11 blade. Lesion completeness was verified visually at the time of surgery. Overlying musculature and skin were then closed. Animals were administered Lactated Ringer’s solution (Baxter Healthcare, Deerfield, IL, USA), cefazolin (10 mg/kg), and buprenex (0.1 mg/kg; Reckitt Benckiser, Slough, United Kingdom) post-operatively. Bladders were manually expressed at least three times per day until sacrifice.
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3

Bladder Injection of Pseudorabies Virus

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Animals were anesthetized with 2% isoflurane for surgery. After the abdomen was shaved and cleaned with a Xenodine solution, rats were placed on the surgical station in supine position. A No. 10 blade was used to make a surgical lesion on the lower abdominal wall to expose the bladder. A total of 6 μL of PRV-152 (Bartha strain, 109 pfu/mL, courtesy of Dr. Michael A. Lane), encoding for green fluorescent protein (GFP), was injected into the bladder detrusor at three different sites, including the front, and bilateral sides, 2 μL per site, with a 10 μL Hamilton syringe connected with a fine glass tip.14 (link),15 (link) Injection sites were immediately sealed with a small drop of tissue glue. Overlying musculature and skin were then closed. Animals were administered with cefazolin (10 mg/kg) and buprenex (0.1 mg/kg; Reckitt Benckiser, Slough, United Kingdom) post-operation.
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4

Spinal Cord Transection in Rodents

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Animals were anesthetized with 2% isoflurane. A partial laminectomy was performed at T8/9 vertebra to expose the dorsal spinal cord. To completely remove supraspinal control and the possibility of formation of descending propriospinal projections postinjury, animals underwent a complete spinal cord transection at the 10th thoracic (T10) level using a no. 11 blade. Lesion completeness was verified visually at the time of surgery. After active bleeding stopped, overlying musculature and skin were closed and lactated Ringer’s solution (3 ml, Baxter Healthcare), cefazolin (10 mg/kg), and buprenex (0.1 mg/kg; Reckitt Benckiser) were subcutaneously administered. Bladders were manually expressed at least three times daily until killing.
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5

Spinal Transection for Micturition Reflex

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To determine whether spinal TH+ interneurons are involved in recovered micturition reflex circuitry, we performed a complete spinal cord transection at the 10th thoracic level (T10-TX) to completely remove supraspinal control as well as some propriospinal projections onto spinal micturition neuronal circuits. Animals were anesthetized with 2% isoflurane. A partial laminectomy was performed at the T8 vertebrae to expose the dorsal spinal cord. The spinal cord was completely transected at T10 using a No. 11 blade. Lesion completeness was verified visually at the time of surgery. Overlying musculature and skin were then closed. Animals were administered lactated Ringer's solution (Baxter Healthcare, Deerfield, IL), cefazolin (10 mg/kg), and burprenex (0.1 mg/kg; Reckitt Benckiser, Slough, UK) post-operatively. Bladders were manually expressed two to three times daily until euthanized.
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