GuidelinesfortheUseofAnalgesicsandTranquilizersinLaboratoryAnimal2

General

Some of the drugs listed here do not possess all three criteria for an anesthetic and must be used in combinations to achieve full anesthesia or may be administered individually for restraint, sedation or analgesia. Dosages for specific animals are linked from RAR's formulary. Often injectable drugs are used in combinations. These drugs tend to have synergistic effects. Mixing them can significantly reduce the dosage needed for any individual drug. 

As with inhalation anesthesia, injectables are given to effect. Dosages listed are guidelines. Effects may vary among individuals. If a drug is scheduled by the Controlled Substances Act of 1970, licenses are required to purchase them, and written records must be kept of their use. Universitypolicy outlines these requirements.  Anesthetic drugs that have exceeded their expiration date may not be used, even for terminal procedures 

Injectable anesthetics are, in general, metabolized by the liver and excreted by the kidneys. Animals with liver or kidney disease should not be anesthetized with these agents. Inhalation anesthetics are safer for use in sick or debilitated animals, because there is minimal metabolism, the amount of anesthetic administered can be controlled and one can cease administration as the situation dictates. Injectable anesthetics offer the advantage of requiring less expensive equipment. 

Local Anesthetics

The generic and brand names of local anesthetics often have the suffix "caine". Common local anesthetics are procaine (Novacaine), bupivicaine, lidocaine (Xylocaine) and proparicaine. Considerable experience and skill are necessary in the administration of local anesthetics to animals, and aseptic techniques must be employed. Some animals must be sedated before local anesthetics are injected. 

Local anesthetics may be administered by several techniques. Anesthetic effects are seen within 15 minutes of administration and may last from 45 minutes to several hours, depending on the drug used.

• Infiltration or infusion- injection beneath the skin and other tissue layers along the site of an incision before or after a procedure

• Field block, ring block- injection into soft tissues distant from the actual incision in a pattern that intersects the nerve supplying the surgical site

• Nerve conduction block- infusion of a small amount of drug or directly adjacent to the sheath of a nerve supplying the surgical site 

• Regional or spinal anesthesia- injection into the vertebral canal, epidurally or into the sub-arachnoid space. To avoid systemic toxicity, care must always be taken not to inject local anesthetics into blood vessels. 

• Topical local anesthetics, such as lidocaine jelly, may be useful for some surgical wounds. 

• Proparicaine may be used as a local anesthetic during retroorbital blood collection from mice. One drop on the eye, wait 10-15 minutes before performing the procedure.

An interesting use of local anesthetics is for amphibian and fish anesthesia. Tricaine and benzocaine can be added to water at a dose of from 25-100 mg/L, depending on the depth of anesthesia required. When the fish loses equilibrium (floats belly up) or an amphibian becomes inactive, it can be handled. For longer procedures, intermittent supplementation of anesthetic treated water to the gills or skin may be required. The animal is recovered in fresh water. 

Phenothiazine and Buterophenone Sedatives

These sedatives include acepromazine, chlorpromazine, droperidol (Innovar-Vet) and azaperone(Stresnil). These drugs have excellent sedative properties, as well as muscle relaxation, antiemetic and antiarrhythmogenic effects. They have no analgesic activity, but when administered with other anesthetics can potentiate their effect. Acepromazine is the most commonly used. It is recommended as a sole sedative in dogs and as an anesthetic premedication to improve both induction and recovery (it is long acting) in all species. Droperidol is usually only available in combination with the narcotic, fentanyl (Innovar-vet) and has been associated with aggressive behavior in dogs. 

Disadvantages of these sedatives are that they are alpha adrenergic blockers and cause peripheral vasodilation which can lead to hypothermia. They may have prolonged activity in sight hounds. Acepromazine and chlorpromazine decrease seizure threshold, and are contraindicated in animals with CNS lesions. Because these sedatives lack analgesic activity it is important to realize that any painful stimulation of the animal may cause it to emerge rapidly from the sedated state. 

Benzodiazapines

The benzodiazapines include diazepam (Valium), midazolam (Versed) and zolazepam (Telazol). These drugs are anti-anxiety and anticonvulsant drugs with good muscle relaxation. They have minimal cardiovascular and respiratory effects. Sedation is minimal in most species, except for swine and nonhuman primates. The primary use of these drugs in anesthesia is in combination with other drugs. Ketamine-diazepam, midazolam-narcotic, and tiletamine-zolazepam (Telazol) combinations can be very useful for induction of general anesthesia and for short procedures. These drugs are regulated by the Controlled Substances Act and require special record keeping. 

Thiazines

The thiazine derivatives include xylazine and medetomidine. These two drugs are very similar. They are alpha-2 adrenergic agonists. They cause CNS depression resulting in sedation, emesis and mild analgesia. They also cause hypotension, second degee atrio-ventricular block and bradycardia. Occasionally, aggressive behavior changes have been seen in dogs. They are very useful in combination with other drugs, like ketamine for anesthesia in rodents and swine. They are best avoided in dogs, cats and nonhuman primates, primarily because their significant side-effects can be avoided by using other drugs. They can be used alone for minor procedures in ruminants. It is important to note that the dose for these drugs in ruminants is 1/10 that used in other species. The effects of the thiazine derivatives can be reversed with yohimbine or atapimazole. Use of these drugs with the reversal agent shortens anesthetic recovery and greatly expands the safety and utility of these drugs. Xylazine is a potent analgesicin frogs appropriate for relief of post-surgical pain.

Opiates

The opiates, sometimes referred to as narcotics,are a large class of drugs that exert their effects on the opiate receptors in the central nervous system. Depending on the receptors a drug is active against, and the type of action it has on the receptor, the effects of narcotics can be primarily analgesic, as with buprenorphine (Buprenex), pentazocine (Talwin) and nalbuphine (Nubain), or a mixture of analgesia and euphoria with sedation as with butorphanol (Torbugesic), fentanyl (Innovar-Vet), morphine, meperidine (Demerol) or oxymorphone. Opiates have little effect on the myocardium. However, there can be significant respiratory depression, as well as other side-effects such as nausea and vomiting, delayed gastric emptying, hypotension, and bradycardia. Some species may develop hyperexcitability if given certain opiates. These side-effects are seen more with the mixed effect opiates than the pure analgesics. Naloxone is a opiate antagonist that can be used to reverse the effects of other narcotics. Other opiates, like buprenorphine, nalbuphine and nalorphine, have mixed agonist-antagonist effects and may interfere with the effects of concurrently administered narcotics. All opiates are controlled substances and their use requires special record keeping. These drugs can be given alone as a post-procedural analgesic or in combination with other agents to provide balanced anesthesia, restraint with analgesia for minor procedures, or can be used to decrease the dose of an anesthetic that is needed to provide a surgical plane of anesthesia. 

Don't forget to follow the University Controlled Substances Policy